Alcon Jobs

At Alcon, we are driven by the meaningful work we do to help people see brilliantly. We innovate boldly, champion progress, and act with speed as the global leader in eye care. Here, you'll be recognized for your commitment and contributions and see your career like never before. Together, we go above and beyond to make an impact in the lives of our patients and customers. We foster an inclusive culture and are looking for diverse, talented people to join Alcon and we are looking for a Principal, Biostatistics Statistical Programming either in Fort Worth, TX or to work remotely. In this role, a typical day will include: * Lead onboarding, professional development, training and mentoring assigned programmers Understand SP deliverables, customer expectations and resource requirements. Prioritize tasks, assign resources, and manage plan to optimize resources. * Forecast short-term and long-term demand for resources * Generate status reports and metrics * Lead statistical programming activities as Project Programmer for assigned studies or project-level activities including requirements analysis, resource estimation, planning and tracking, development of programs and validation of deliverables * Develop and review programming dataset specifications * Coordinate activities of all programmers assigned to the same study or project. Conduct kickoff meeting to provide an overview of the study or project, discuss deliverables, roles and responsibilities, timelines, and conventions * Remove barriers to facilitate quality, timely and efficient completion of deliverables. Ensure that programmers have all required inputs for their tasks * Provide solutions to programming issues and/or ensure efficient implementation * Build and maintain effective working relationships with relevant team functional representation. Effectively communicate the status of deliverables, changes to plan, risks and proposed mitigation strategy to relevant team and supervisor * Contribute to development of SP standards and processes, knowledge sharing and other tasks as assigned * Responsible for quality control and audit readiness of all assigned statistical programming deliverables as well as accuracy and reliability of statistical analysis results. Additional Experience: * Effectiveness in developing, mentoring and managing assigned programmers * Efficiency of resource utilization and accuracy of resource estimation * Quality and timeliness of all deliverables for assigned studies or project-level activities * Ability and effectiveness in leading activities and coordinating programmers assigned to the same study or project * Adequate representation as Trial Programmer in the Clinical Trial Team. Effectiveness of communication and participation as assessed by the team members * Compliance with internal and external standards as measured by audit findings * 5 years of relevant programming experience * 2 years of proven ability to lead statistical programming activities as Trial Programmer * Relevant programming experience is in the pharmaceutical or medical device industry * Proven ability to lead statistical programming activities as Project Programmer Impact in the Organization: * Timely and high-quality SP deliverables. Delays and errors in deliverables may impede submissions or other product developments and subsequent revenue loss to the company * Efficient programming leading to quality submissions, and reduced time and costs for development and registration * Ensuring external quality reputation of Alcon with Health Authorities Competency Profile: * Strong leadership, collaboration and organizational skills with proven ability to successfully manage numerous, simultaneous activities and meet deadlines * Strong SAS programming skills including development and use of macros * Extensive experience in requirements analysis, resource estimation, planning and tracking deliverables and coordinating activities * Extensive experience in developing programming dataset specifications * Good working knowledge of statistical concepts * Good understanding of regulatory requirements relevant to Statistical Programming (e.g. GCP, ICH) and industry standards such as CDISC * Excellent interpersonal skills and proven ability to operate effectively in a global environment. Ability to influence and communicate across functions * Excellent written and oral communication * Interviewing, mentoring, coaching, knowledge management and best practice sharing What You'll Bring to Alcon: * Bachelor's Degree or Equivalent years of directly related experience (or high school +13 yrs; Assoc.+9 yrs; M.S.+2 yrs; PhD+0 yrs) * The ability to fluently read, write, understand, and communicate in English * 5 Years of Relevant Experience How You Can Thrive at Alcon: * Join Alcon's mission to provide outstanding, innovative products and solutions to improve sight, improve lives, and grow your career! * Alcon provides robust benefits package including health, life, retirement, flexible time off, and much more! * Travel Requirements: 0-5% * Relocation assistance: Yes * Sponsorship available: Yes Alcon Careers See your impact at alcon.com/careers #LI-DNI ATTENTION: Current Alcon Employee/Contingent Worker If you are currently an active employee/contingent worker at Alcon, please click the appropriate link below to apply on the Internal Career site. Find Jobs for Employees Find Jobs for Contingent Worker Alcon is an Equal Opportunity Employer and participates in E-Verify. Alcon takes pride in maintaining a diverse environment and our policies are not to discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, gender identity, marital or veteran status, disability, or any other legally protected status. Alcon is also committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please send an email to *************************** and let us know the nature of your request and your contact information.

At STERIS, we help our Customers create a healthier and safer world by providing innovative healthcare and life science product and service solutions around the globe. SPM Client Service Account Manager As a SPM Client Services Account Manager at STERIS, you are tasked with providing excellent Customer support while ensuring KPIs for Customer satisfaction and continued business growth are met. You will serve as the primary partner with our Customers to ensure our SPM software is meeting their needs and enhancing the operation of their sterile processing departments while focusing on Customer-focused initiatives. You will be expected to drive success and lead the team as they provide excellent support to our Customers, meet high expectations, and develop a strong partnership with our Customers. This is a remote based Customer facing position. To support and service our Customer in this assigned territory candidates must be based out of one of the following state: Denver, CO or Salt Lake City, Utah What you will do as a Client Services Account Manager * Lead current Customers in identifying additional solutions to help increase their utilization of SPM (interfaces, modules, mobile hand scanners) and provide excellent Customer support while ensuring KPIs for Customer satisfaction and continued business growth are met. * Work with Customers on recommendations for strategic adjustments to maximize Customer satisfaction and growth opportunities for SPM business. * Lead initiatives and implementation for annual software upgrades, new feature adoptions, and new products and services. * Identify and establish site visits to coordinate and execute assigned implementations of modules, services, and interface for Customers. Identify opportunities for additional reoccurring revenue through products and services based on Customer's needs and requirements. * Manage assigned Customer renewals of their technical support and upgrade service agreement. * Provide training and Customer support to help Customers increase their utilization of SPM and satisfaction with the products. * Lead the remediation and mitigation of Customer issues and for at-risk Customers throughout the region. * Maintain a thorough understanding of software capabilities and use this understanding to provide solutions for Customers. * Partner with sales, implementation, and other commercial teams to drive on-site visits for business analysis, system configuration, and continued education to drive upgrade proposals to the Customer. * Collaborate with internal STERIS teams to drive overall Customer satisfaction. The Experience, Skills and Abilities Needed Required: * Bachelor's degree * 5 years of project management experience implementing software and/or hardware within Customers in an enterprise IT organization * In lieu of Bachelor's degree, Associate's degree with 9 years of related experience OR High School diploma with 13 years of related experience * Ability to complete the Certified Central Service Vendor Partner (CCSVP) certification within the first year of employment * Must be able to be compliant with hospital/customer credentialing requirements Preferred: * General knowledge of software, servers, IP addresses, networking concepts (DHCP, Static IP, etc.) * Experience in sterile processing departments What STERIS Offers We value our employees and are committed to providing a comprehensive benefits package that supports your health, well-being, and financial future. Here is just a brief overview of what we offer: * Base Salary + Incentive Compensation Program * Vehicle Reimbursement Plan (includes monthly stipend + mileage reimbursement) * Cell Phone Stipend * Robust Training Program * Paid Time Off + 9 Corporate Holidays Per Year * Excellent Healthcare, Dental, and Vision Benefits * Healthcare and Dependent Flexible Spending Accounts * Long/Short Term Disability Coverage * 401(k) with a Company Match * Parental Leave * Tuition Reimbursement Program * Additional Add-On Benefits/Discounts Must be able to be compliant with hospital/customer credentialing requirements #LI-BS1 Pay range for this opportunity is $67,750.00 - $94,762.50. This position is eligible for bonus. Minimum pay rates offered will comply with county/city minimums, if higher than range listed. Pay rates are based on a number of factors, including but not limited to local labor market costs, years of relevant experience, education, professional certifications, foreign language fluency, etc. STERIS offers a comprehensive and competitive benefits portfolio. Click here for a complete list of benefits: STERIS Benefits STERIS is a leading global provider of products and services that support patient care with an emphasis on infection prevention. WE HELP OUR CUSTOMERS CREATE A HEALTHIER AND SAFER WORLD by providing innovative healthcare, life sciences and dental products and services. STERIS is a $5 billion, publicly traded (NYSE: STE) company with approximately 17,000 associates and Customers in more than 100 countries. If you need assistance completing the application process, please call ****************. This contact information is for accommodation inquiries only and cannot be used to check application status. STERIS is an Equal Opportunity Employer. We are committed to equal employment opportunity and the use of affirmative action programs to ensure that persons are recruited, hired, trained, transferred and promoted in all job groups regardless of race, color, religion, age, disability, national origin, citizenship status, military or veteran status, sex (including pregnancy, childbirth and related medical conditions), sexual orientation, gender identity, genetic information, and any other category protected by federal, state or local law. We are not only committed to this policy by our status as a federal government contractor, but also we are strongly bound by the principle of equal employment opportunity. The full affirmative action program, absent the data metrics required by § 60-741.44(k), shall be available to all employees and applicants for employment for inspection upon request. The program may be obtained at your location's HR Office during normal business hours. Req ID: 48372 Job Category: Customer Operations/Customer Support Location: Denver, CO, US, 80012 Workplace Type: Remote STERIS Sustainability Life at STERIS

At STERIS, we help our Customers create a healthier and safer world by providing innovative healthcare and life science product and service solutions around the globe. Repair Technician 1 - Glendale, CA * When surgical instruments are sharpened and working properly, surgeons can focus on providing the best care for their patients. STERIS offers a variety of repair solutions to meet the needs of the Customer including onsite mobile repair services, in house repair lab services, or one of five national repair centers. * You do not have to have previous instrument repair experience to be considered. * This is an entry level job - we will train you! * Click this link to take a peek at the truck and the work you could be doing to help STERIS create a safer, healthier world! * In this position, you will perform surgical instrument inspection, repair, and refurbishment in a field-based setting. Technicians work out of mobile repair trucks at Customer sites and regional labs in more condensed markets. Technicians deliver superior Customer Experience by providing timely and quality repairs to meet compliance standards. * This position may require occasional overnight travel. * This role requires daily travel by driving a company vehicle. If offered this position, STERIS will run a 7 year driving record check, as part of our onboarding process. * This is a remote based customer facing position. To support and service our customers in this assigned territory candidates must be based out of California. * PLEASE NOTE: This position requires 50% overnight travel, which is usually comprised of Monday-Friday travel every other week to service accounts several hours away. STERIS covers all travel expenses, and driving time is paid. What You Will Do As A Repair Technician Level 1 * Perform basic to intermediate inspection and repairs on surgical instrumentation using grinding wheels, buffing wheels, various hand and power tools, soldering, etc. Complexity of repairs and level of intricacy will vary. * You will work in the field on a mobile repair truck, inside a repair lab or inside a hospital, based on the needs of the Customer within the assigned territory. * Provide invoicing and documentation based on business need. * Provide support various locations within assigned territory depending on the service agreements, Customer needs, and staffing levels. What STERIS Offers * Competitive pay * Overtime opportunity * Annual merit review and incentive plans * Uniforms and all necessary tools provided * Business travel and all related expenses paid * Medical, vision, prescription, dental and life insurance * 401(k) with a company match * Paid time off that accrues from day one and paid holidays * Tuition assistance * Opportunities for advancement * Competitive pay and quarterly incentive opportunity * Extensive hands-on training and development * Career progression path with STERIS Instrument Management Services and growth opportunities in other parts of STERIS * Medical, vision, dental, life insurance, 401(k) with a company match, tuition assistance, and paid vacation time and paid holidays The Experience, Skills, and Abilities Needed: * High school diploma or GED required * 2+ years of work experience, including at least 1 year of relevant experience*, or 1 year of experience at STERIS. All experience must be verifiable. * Must be able to meet flexible schedules with early/late hours and occasional overnight/out of state travel, based on Customer and business needs. * Must be able to pass a DOT medical/ physical exam and comply with all DOT regulations. * Must have a valid driver's license with an acceptable driving record (CDL not required) and maintain required vaccines. * Ability to drive DOT regulated vehicle and conduct basic box truck safety checks. * Must be at least 21 years old to meet the FMCSA age requirement for commercial interstate driving. * Must be able to lift up to 25 pounds at times and push instrument carts ranging from 10-150 pounds at times. * Must be able to be compliant with hospital/customer credentialing requirements * What is relevant work experience? * Hands-on repair, assembly, or product testing and use of small hand tools is a plus. Examples are small engine repair, cell phone and electronics repair, testing, or re-builds, carpentry, circuit board assembly and repair, sterile processing, industrial sewing, and jewelry repair. Maintenance, construction, welding, fabrication, and automotive repair can also be relevant. #LI-AC1 Pay range for this opportunity is $24.00 - $26.00/hour. Minimum pay rates offered will comply with county/city minimums, if higher than range listed. Pay rates are based on a number of factors, including but not limited to local labor market costs, years of relevant experience, education, professional certifications, foreign language fluency, etc. Employees (and their families) may enroll in our company-sponsored medical, dental, vision, flexible spending, health savings account, voluntary benefits, supplemental life/AD&D plans and the company's 401k plan. Employees are covered by an employee assistance program (also available to household members) and long-term disability. Full-Time Employees are also eligible for short-term disability. Full-time Employees will also receive Paid Time Off (PTO) based on years of service and paid Holidays. Part-time employees working 20 or more hours receive a pro-ration of the full-time PTO allocation and paid Holidays based on their standard hourly work week. Full-Time employees are eligible for four weeks of paid parental leave. Part-time employees also receive paid parental leave, pro-rated based on their standard hourly work week. STERIS is an Equal Opportunity Employer. We are committed to equal employment opportunity and the use of affirmative action programs to ensure that persons are recruited, hired, trained, transferred and promoted in all job groups regardless of race, color, religion, age, disability, national origin, citizenship status, military or veteran status, sex (including pregnancy, childbirth and related medical conditions), sexual orientation, gender identity, genetic information, and any other category protected by federal, state or local law. We are not only committed to this policy by our status as a federal government contractor, but also we are strongly bound by the principle of equal employment opportunity. Req ID: 47062 Job Category: Service/Technical Services Location: Glendale, CA, US, 91020 Workplace Type: Remote Life at STERIS STERIS Sustainability

HOW MIGHT YOU DEFY IMAGINATION? You've worked hard to become the professional you are today and are now ready to take the next step in your career. How will you put your skills, experience and passion to work toward your goals? At Amgen, our shared mission-to serve patients-drives all that we do. It is key to our becoming one of the world's leading biotechnology companies, reaching over 10 million patients worldwide. Come do your best work alongside other innovative, driven professionals in this meaningful role. Associate Manufacturing I - Nights Live What you will do Let's do this! Let's change the world! In this vital role you will perform operations in the Manufacturing area. Operations will be performed according to Standard Operating Procedures (SOPs), these can include bioreactor cleaning, steaming, inoculation, etc., operations. Perform and monitor critical processes, complete routine validation protocols, and regularly draft and revise documents such as Manufacturing Procedures, SOPs, and technical reports. Perform basic troubleshooting and assist in the review of documentation for assigned functions. Participate on cross-functional teams and represent the manufacturing teams. May also have the responsibility of owning deviations/CAPAs. Identify, recommend, and implement improvements related to routine functions. This position is for the AR5 A shift Upstream Cell Culture (Perfusion, Production, Harvest - PPH) team. The successful candidate will be expected to join a shift team working a 12-hour shift. The shift pattern will be 7PM-7AM with a two-week rotation covering 7 days per week. The rotating shift offers several benefits, with an average of 14 days on shift per month with every other weekend off. In addition, any Sundays worked receive Premium pay. Qualifications Win What we expect of you We are all different, yet we all use our unique contributions to serve patients. The dedicated professional we seek is an excellent teammate with these qualifications. Basic Qualifications: High school/GED + 2 years of manufacturing or operations work or military experience OR Associate's + 6 months of manufacturing or operations work or military experience Preferred Qualifications: Bachelor's degree in Science or Engineering Knowledge of large-scale biotechnology operations such as purification, cell culture, aseptic processing, etc. Knowledge of Single-use-Systems CFR and Regulatory knowledge Mechanical ability/expertise Basic statistical mathematical skills Ability to interpret and apply GMP knowledge Understanding of analytical methods for manufacturing area Demonstrated technical writing capability Able to demonstrate project management skills and presentation skills Ability to understand, apply and evaluate basic chemistry, biology and physical principles Basic troubleshooting skills on production equipment Experience with Delta V Experience with lab equipment/testing Additional Information Thrive What you can expect of us As we work to develop treatments that take care of others, we also work to care for our teammates' professional and personal growth and well-being. The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications. Amgen offers a Total Rewards Plan comprising health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities including: Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts. A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan Stock-based long-term incentives Award-winning time-off plans and bi-annual company-wide shutdowns Flexible work models, including remote work arrangements, where possible Apply now for a career that defies imagination Objects in your future are closer than they appear. Join us. careers.amgen.com Application deadline Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position. Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. All your information will be kept confidential according to EEO guidelines.

**Join Amgen's Mission of Serving Patients** At Amgen, if you feel like you're part of something bigger, it's because you are. Our shared mission-to serve patients living with serious illnesses-drives all that we do. Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest diseases. With our focus on four therapeutic areas -Oncology, Inflammation, General Medicine, and Rare Disease- we reach millions of patients each year. As a member of the Amgen team, you'll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you'll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career. **Global Safety Director, Obesity - US, Remote** **What you will do** Let's do this. Let's change the world. In this vital role you will serve as the safety expert of the assigned product(s) within the Obesity portfolio. You will establish the strategy, direction, and priorities of pharmacovigilance activities and are accountable for the overall safety profile and all product-related decisions and deliverables for assigned products. You will also lead the Safety Analysis Team (SAT), Global Safety Team (GST) and is a core member of the Executive Safety Committee (ESC). Serve as a member of the Evidence Generation Team and other relevant cross-functional teams and will be assigned as delegated for the Therapeutic Area Head (TAH). Work in a fast-paced environment with a dynamic team of safety physicians and scientists dedicated to bringing important therapies to patients in need. Key activities: + Validate safety signals and lead safety signal assessments + Develop and maintain Core Safety Information (core data sheet, core risks in informed consent forms, etc.) + Prepare/review core and regional risk management plans including additional risk minimization measures + Prepare/review safety sections of periodic aggregate reports + Provide safety input to protocols, statistical analysis plans, and clinical study reports + Prepare/review safety sections of new drug applications and other regulatory filings + Serve as safety expert on Evidence Generation Team for assigned products + Inspection Readiness + Domestic and International travel up to 10% **What we expect of you** We are all different, yet we all use our unique contributions to serve patients. The Global Safety Director professional we seek is a leader with these qualifications: **Basic Qualifications:** Doctorate degree and 4 years Safety experience OR Master's degree and 7 years Safety experience OR Bachelor's degree and 9 years Safety experience **Preferred Qualifications:** + Product safety in the bio/pharmaceutical industry or regulatory agency + Expertise in Obesity, Metabolic/CV therapeutic area, or clinical training. + Experience with marketed product safety; risk management + Experience with phase 1-3 clinical trials safety assessments and analyses + Drug Submission experience + Leadership experience of the safety profile of products assigned with cross-functional team members. **What you can expect of us** As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we'll support your journey every step of the way. The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is $184,901. to $233,959. Actual salary will vary based on several factors including, but not limited to, relevant skills, experience, and qualifications. In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include: + A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts + A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan + Stock-based long-term incentives + Award-winning time-off plans + Flexible work models, including remote and hybrid work arrangements, where possible **Apply now** **for a career that defies imagination** Objects in your future are closer than they appear. Join us. **careers.amgen.com** In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information. **Application deadline** Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position. As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease. Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. \#obesity

At STERIS, we help our Customers create a healthier and safer world by providing innovative healthcare and life science product and service solutions around the globe. As an IMS Inside Sales Representative II at STERIS, you will manage sales and Customer activities in an assigned Inside Sales territory. You are expected to achieve maximum sales profitability, growth and account penetration by building relationships, understanding Customer needs, selling the Instrument Management Services (IMS) portfolio of services and products, and prospecting revenue opportunities. This can be a remote position, based anywhere in the United States. What you will do as an Inside Sales Representative * Collaborate with field sales and sales support teams to identify and close new business. * Partner with field service teams assigned to territory including facilitating introductions with Customers. * Attend Customer training events throughout the year such as Customer Learning Seminars. * Responsible for providing the quarterly business reviews, proactive maintenance inspections, departmental evaluations, and in-services to accounts in territory either virtually or in person. * Update the CRM system as required to document Customer information, sales activities, purchase orders. * Resolve Customer service issues such as tracking down delayed repairs and billing issues and escalate as needed. * Develop relationships with chapters of industry groups and GPOs within the territory. The Experience, Skills, and Abilities Needed Required * High School diploma * 3 years successful sales experience (proven track record of achieving goals) * Ability to travel overnight up to 50% * Valid Driver's License * Industry certifications such as IAHCSMM, AORN, CCSVP, SGNA preferred (or able to obtain in first year of employment) * Must be able to be compliant with hospital/customer credentialing requirements Preferred * Bachelor's degree * Medical device/Service Sales/B2B experience * Military Experience / Security Clearance What STERIS Offers We value our employees and are committed to providing a comprehensive benefits package that supports your health, well-being, and financial future. Here is just a brief overview of what we offer: * Base Salary + Incentive Compensation Program * Cell Phone Stipend * Robust Sales Training Program * Paid Time Off + 9 Corporate Holidays Per Year * Excellent Healthcare, Dental, and Vision Benefits * Healthcare and Dependent Flexible Spending Accounts * Long/Short Term Disability Coverage * 401(k) with a Company Match * Parental Leave * Tuition Reimbursement Program * Additional Add-On Benefits/Discounts Pay range for this opportunity is $50,000. This position is eligible for bonus participation. Minimum pay rates offered will comply with county/city minimums, if higher than range listed. Pay rates are based on a number of factors, including but not limited to local labor market costs, years of relevant experience, education, professional certifications, foreign language fluency, etc. STERIS offers a comprehensive and competitive benefits portfolio. Click here for a complete list of benefits: STERIS Benefits STERIS is a leading global provider of products and services that support patient care with an emphasis on infection prevention. WE HELP OUR CUSTOMERS CREATE A HEALTHIER AND SAFER WORLD by providing innovative healthcare, life sciences and dental products and services. STERIS is a $5 billion, publicly traded (NYSE: STE) company with approximately 17,000 associates and Customers in more than 100 countries. If you need assistance completing the application process, please call ****************. This contact information is for accommodation inquiries only and cannot be used to check application status. STERIS is an Equal Opportunity Employer. We are committed to equal employment opportunity and the use of affirmative action programs to ensure that persons are recruited, hired, trained, transferred and promoted in all job groups regardless of race, color, religion, age, disability, national origin, citizenship status, military or veteran status, sex (including pregnancy, childbirth and related medical conditions), sexual orientation, gender identity, genetic information, and any other category protected by federal, state or local law. We are not only committed to this policy by our status as a federal government contractor, but also we are strongly bound by the principle of equal employment opportunity. The full affirmative action program, absent the data metrics required by § 60-741.44(k), shall be available to all employees and applicants for employment for inspection upon request. The program may be obtained at your location's HR Office during normal business hours. Req ID: 48151 Job Category: Sales Location: Birmingham, AL, US, 35222 Workplace Type: Remote STERIS Sustainability Life at STERIS

The Principal Business Analyst (BA) in Research and Preclinical Development IT will collaborate with Research Scientists acting as a liaison defining and delivering data management solutions. The BA interfaces between Research Systems Analysts, Programmers, Data Architects, Scientists, and IT Project Managers ensuring information technology designs meet the needs of the end users. In addition, we ensure our solutions meet the requirements by engaging the team in an iterative software development cycle This position will required you to be on-site for 3+ days/week at our Tarrytown, NY offices. We cannot offer a fully remote option. If eligible, we can offer relocation assistance. A typical day may include the following: * Lead scientific-related business needs assessment and design, build and implementation of IT systems. Work with scientists and laboratory personnel understanding business processes and suggesting improvement opportunities. * Define user requirements and design plans solutions into the Research systems architecture through documentation of scientific processes, data workflows, and product/service requirements * Collaborate with end-users and technical teams translating high-level business and user requirements into functional and design specifications. * Act as an expert technical and scientific resource to software development staff in all phases of the development and implementation process * Participate in user research, usability and acceptance testing * Understand system interdependencies and collaborate with project teams accordingly * Assist in evaluating cost-benefit and return on investment analyses * Train, develop and manage junior scientific business analysts * Contributes to the definition, implementation and governance of the BA practices and processes. * May lead or supervise a small team (e.g., 1 - 3 people), assigning day-to-day work. This may be for you if you have: * Strong ability to collaborate with business functional leaders, across all levels in the business supported organization and with technologists. * Experience with critical functional data and management processes, and data integration. * Collaborative, agile approach to drive speedy, creative and efficient use of technology and data to drive business value across IT. * Ability to creatively and constructively challenge designs to ensure simplicity and supportability. * Capable of translating and presenting concepts into practical business terms in both small and large group settings. * Ability to analyze and document complex data management processes. * Ability to think analytically and interpret relevant data and information. To be considered, you must have an Advanced degree (MS or PhD) and 5+ years of scientific experience, including 2+ years in a data, business analyst or relevant IT project execution role. Experience in business process & requirements gathering through is execution. Your Research experience will need to include some of the following: (e.g., biologic and/or small molecule drug discovery, cell biology, molecular biology, immunology, and/or invivo studies). Preferred experiences * Business intelligence tools such as Spotfire, Tableau, Qliksense, Vortex, Power BI. * Project Management of Research programs in a pharmaceutical setting or use of PPM systems to manage projects. Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive and diverse culture that provides comprehensive benefits, which often include (depending on location) health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees at all levels! Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business. For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location. Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc. Salary Range (annually) $113,100.00 - $184,700.00

Career CategoryMedical AffairsJob DescriptionJoin Amgen's Mission of Serving Patients At Amgen, if you feel like you're part of something bigger, it's because you are. Our shared mission-to serve patients living with serious illnesses-drives all that we do. Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest diseases. With our focus on four therapeutic areas -Oncology, Inflammation, General Medicine, and Rare Disease- we reach millions of patients each year. As a member of the Amgen team, you'll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you'll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career. Medical Science Liaison, Nephrology - Rare Disease Territory: Pacific Northwest Region Territory Includes - AK, WA, OR, ID, MT, WY, UT, CO What you will do Let's do this. Let's change the world. In this vital role you will serve as a scientific liaison to the medical/scientific community and will be responsible for establishing, developing and maintaining relationships with prominent experts and clinicians throughout the Pacific Northwest Region. Responsibilities: Network and partner with important external customers, including medical thought leaders, academic institutions, large group practices, medical directors, managed care decision makers, and pharmacy directors in alignment with applicable compliance, legal, and regulatory guidelines. Understand, integrate and effectively communicate scientific/medical information and commercial value of products to the medical community and other key internal and external audiences. Prioritize and work effectively in a self-directed manner in a constantly changing environment, including ability to obtain, integrate, and communicate customer feedback. Pair customers' unmet needs with available internal resources. Collaborate effectively with all functional areas to identify opportunities and needs that can be addressed via communication of scientific, medical, and health economic information. Identify potential new speakers and train on scientific content for sponsored external speaker programs. Participate in national and regional conferences, meetings, and other scientific venues as appropriate to support the Medical/Clinical strategy and to obtain new competitive information, keep abreast of clinical trends, and support and maintain relationships with key investigators and scientific research. Working in conjunction with the medical affairs and clinical development teams, evaluate potential external clinical research collaboration opportunities and facilitate the conduct of external clinical investigator-initiated trials (IITs) and company sponsored trials. Monitor the competitive environment for advances and trends in our therapeutic areas, including new treatment management and new therapies, as well as competitive products and features and provide feedback to the senior leadership team on specific initiatives of competitors. What we expect of you We are all different, yet we all use our unique contributions to serve patients. The professional we seek is a go-getter with these qualifications. Basic Qualifications: Doctorate degree & 2 years of Medical Affairs experience OR Master's degree & 6 years of Medical Affairs experience OR Bachelor's degree & 8 years of Medical Affairs experience Preferred Qualifications & Experience: PharmD, MD, DNP, PhD doctorate level degrees preferred. Field Medical Affairs experience preferred. Experience in Nephrology or similar disease state (Transplant, Dialysis, CV/Metabolics, Diabetes) strongly preferred. Rare disease/specialty disease state experience preferred. Exceptional oral and written communication and interpersonal skills (including strong demonstration of ability to network. Ability to travel up to 60% for territory management, attendance at regional and national conferences/workshops, and attendance at company meetings. There may be a need to work up to 15-hour days due to travel Must have ability to learn to use new business applications across hardware tools (e.g., PC, iPad). Proficient in Microsoft Office. Professional, proactive demeanor Strong interpersonal skills. Excellent written and verbal communication skills. What you can expect of us As we work to develop treatments that take care of others, we also work to care for our teammates' professional and personal growth and well-being. The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is listed below. Actual salary will vary based on several factors including, but not limited to, relevant skills, experience, and qualifications. In addition to the base salary, Amgen offers a Total Rewards Plan comprising health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities including: Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts. A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan Stock-based long-term incentives Award-winning time-off plans and bi-annual company-wide shutdowns Flexible work models, including remote work arrangements, where possible Apply now for a career that defies imagination Objects in your future are closer than they appear. Join us. careers.amgen.com Application deadline Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position. As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease. Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. . Salary Range 165,467.00 USD - 188,730.00 USD

Career CategoryCollege JobJob DescriptionJoin Amgen's Mission of Serving Patients At Amgen, if you feel like you're part of something bigger, it's because you are. Our shared mission-to serve patients living with serious illnesses-drives all that we do. Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest diseases. With our focus on four therapeutic areas -Oncology, Inflammation, General Medicine, and Rare Disease- we reach millions of patients each year. As a member of the Amgen team, you'll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you'll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career. Undergrad Intern - Representation in Clinical Trials (R&D) (Summer 2025) This could be your everyday Let's do this. Let's change the world. This internship will be approximately 12 weeks and includes both project-based and experiential learning. The intern will be an integral member of the Amgen Representation in Clinical Research (RISE) Team, (within Amgen's Research and Development, Global Medical Organization), which is dedicated to improving clinical trial diversity and proportional representation by addressing the systemic issues that deter people from participating in research, especially those who have been historically excluded due to race, ethnicity, sex, age, and other factors. As a member of Amgen's Global Medical Organization, your work, will be highly collaborative across multiple functions and levels within Amgen, including Research & Development, Corporate Affairs, Government Affairs, Health Equity, Advocacy Relations, Diversity, Inclusion & Belonging, and others. You will be uniquely responsible for one or more key projects that will advance the RISE mission: to serve patients by improving the diversity and representation of racial and ethnic minority and other underrepresented populations in Amgen's clinical research through science-based, data-driven strategies and to positively advance this dialogue across the industry. This educational and developmental opportunity will allow you to gain valuable experience in an enriching and scientific environment while completing meaningful projects and developing the following skills: Develop a project charter to map out objectives and identify key stakeholders, timelines, and deliverables Leverage your analytical, leadership, communication, and interpersonal skills to work in teams, identify problems, conduct research, develop recommendations through qualitative and quantitative analysis, and deliver final projects Present your deliverables/findings through various forums including in-person team workshops and a final readout to senior leaders and cross-functional stakeholders Engage in learning activities, network with colleagues across the company, and enjoy full access to Amgen's Employee Resource Groups Here's what it takes to Win We are all different, yet we all use our unique contributions to serve patients. The collaborative individual we seek is hard-working and adaptable with these qualifications: Basic Qualifications Amgen requires that all individuals applying for an undergrad internship or a co-op assignment at Amgen must meet the following criteria: 18 years or older Currently enrolled in a full-time Bachelor's Degree program from an accredited college or university with a 3.0 minimum GPA or equivalent Completion of one year of study from an accredited college or university prior to the internship commencing Enrolled in a full-time Bachelor's degree program following the potential internship or co-op assignment with an accredited college or university Must not be employed at the time the internship starts Student must be located in the United States for the duration of the internship OR co-op Preferred Qualifications Degree concentration(s) in Human Resources, Business Administration, Communications, Psychology, Sociology, English, Public Health, or a similar field Strong written and verbal communication skills Strong interest in public health, community health, social sciences, health equity, health policy, health communications, DEI (diversity, equity, and inclusion), and/or other related fields Strong interpersonal, organization and time management skills Strong problem-solving and critical thinking Some of the vast rewards of working here As we work to develop treatments that take care of others, we also work to care for our teammates' professional and personal growth in addition to their well-being: The base pay range for this opportunity in the U.S. is $24.70 - $28.30 per hour. Build a network of colleagues that will endure and grow throughout your time with us and beyond. Bring your authentic self to the table and become the professional you're inspired to be through accepting a culture that values the diversity of thought and experience and will flex to your strengths and possibilities. Participate in executive and social networking events, as well as community volunteer projects. Apply nowfor an internship/co-op that defies imagination If you feel like you're part of something bigger, it's because you are. Join us. careers.amgen.com Please search for Keyword R-203057 In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information. Application deadline Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position. As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease. Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. . Salary Range -

Career CategoryClinicalJob DescriptionJoin Amgen's Mission of Serving Patients At Amgen, if you feel like you're part of something bigger, it's because you are. Our shared mission-to serve patients living with serious illnesses-drives all that we do. Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest diseases. With our focus on four therapeutic areas -Oncology, Inflammation, General Medicine, and Rare Disease- we reach millions of patients each year. As a member of the Amgen team, you'll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you'll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career. Director, Scientific Communications - TezspireWhat you will do Let's do this. Let's change the world. In this vital role the Director Scientific Communications is the single point of accountability for Holistic Scientific Communications for Tezspire. Reporting to the Executive Director, Scientific Communications, the Director, Scientific Communications partners with key internal team members to develop and drive execution of the scientific communication deliverables in alignment with overall product strategy. This includes strategic planning and development of content, definition of channels, determination of audience, and areas of focus to maximize Amgen's value proposition. This role will partner closely with the operations team on activities such as process alignment, standardization, continuous improvement, and innovation, including use of digital and multi-channel approaches. As a people leader, this person will also be accountable for creating a culture of psychological safety, agility, and diversity to inspire and motivate teams to the highest level of performance. Responsibilities: The Director, Scientific Communications - Tezspire will lead the Tezspire Scientific Communication (SciComm) Team and specific responsibilities of this role include: Support prioritization process and resource allocation to meet program goals on time and within budget. Lead the Tezspire SciComm team to: Develop high-quality strategic plans and scientific and medical content (including publications, medical content, payer-relevant content) to communicate Amgen science in alignment with product strategies Contribute to medical strategy through scientific expertise and defining appropriate, relevant, and innovative channels for delivery of medical and scientific content to reach target audiences Successfully collaborate with external partner to solicit and provide input into shared product SciComm strategic plans Develop, maintain, cultivate, and influence strong relationships with cross-functional colleagues Support the development of educational events and activities in alignment with program goals and objectives. Maintain strong relationship with the product partner company Support development of strategic plans and ensure successful execution of top tier congresses Understand the external landscape and advance the SciComm capability in alignment with evolving regulatory, legal, and industry guidelines and recommendations Ensure compliance with relevant SciComm SOP(s) and system(s) Recruit, retain, and motivate high-performing and empowered staff Effectively manage agency and vendor partnerships Actively support and enhance the career development of employees within SciComm team In partnership with the SciComm Operations Team: Contribute to and participate in governance of, consistent process, and training across the SciComm capability Support the evolution of systems and new technologies, and continuous process improvement, and vendor oversight Evolve procedures and systems, as necessary, to ensure all activities in full compliance with all applicable laws, regulations, policies, and procedures Ensure staff receive appropriate onboarding and ongoing training,,and manage role-based curriculum (RBC) assignments for SciComm roles Partner with Global Learning and Performance to support the annual strategy and execution of training programs to support TA/staff Partner with Med Info to respond to inquiries and conduct literature surveillance What we expect of you We are all different, yet we all use our unique contributions to serve patients. The professional we seek has these qualifications. Basic Qualifications: Doctorate degree & 4 years of Publication OR Medical Communications OR Medical Value and Access OR Medical Strategy Experience Or Master's degree & 8 years of Global Publication OR Medical Communications OR Medical Value and Access OR Medical Strategy Experience Or Bachelor's degree & 10 years of Global Publication OR Medical Communications OR Medical Value and Access OR Medical Strategy Experience In addition to meeting at least one of the above requirements, you must have at least 4 years of experience directly managing people and/or leadership experience leading teams, projects, programs, or directing the allocation or resources. Your managerial experience may run concurrently with the required technical experience referenced above. Preferred Qualifications: Previous leadership within a function and experience managing direct reports 5 or more years of relevant experience in clinical research, patient care, clinical development, medical/scientific affairs and/or basic research Prior experience in Medical Affairs or Clinical Development within the biopharmaceutical industry, and/or clinical or research experience in inflammatory or respiratory diseases Deep understanding of the drug development and commercialization process Deep understanding of clinical trial processes Toolsets/skills required to drive organizational change and translate corporate imperatives into strategic drivers for the function with limited supervision Business process and systems management experience Finance and budget management experience Knowledge of pharmaceutical industry guidelines and legal/health system environment Strong ability to lead multiple disciplines and initiatives in a fast-paced environment, with changing priorities and significant time pressures to shape functional strategy Exceptional interpersonal, organizational, leadership, and problem-solving skills Exceptional communication skills (written and verbal), time management, project planning, aptitude in presenting in front of executives and strong ability for self-direction Knowledge and experience with multi-channel scientific platform and communications Deep understanding of Good Publication Practices, including familiarity with external guidelines, recommendations and standards (e.g., ICMJE, current Good Publication Practice (GPP) Guidelines, GPP 2022) Externally recognized as having knowledge or expertise in scientific publications, medical communications, or medical affairs practices What you can expect of us As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we'll support your journey every step of the way. The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications. In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include: A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan Stock-based long-term incentives Award-winning time-off plans Flexible work models, including remote and hybrid work arrangements, where possible Apply now for a career that defies imagination Objects in your future are closer than they appear. Join us. careers.amgen.com In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information. Application deadline Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position. As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease. Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. . Salary Range 202,895.00 USD - 232,809.00 USD

JOB ID: R-192788 LOCATION: US - California - Thousand Oaks WORK LOCATION TYPE: On Site DATE POSTED: Oct. 11, 2024 CATEGORY: Human Resources SALARY RANGE: 85,245.00 USD - 109,212.00 USD HOW MIGHT YOU DEFY IMAGINATION? You've earned your degree. How will you use that achievement to reach your goals? Do more with the knowledge you've worked hard to acquire and the passion you already have. At Amgen, our shared mission-to serve patients-drives all that we do. It is key to our becoming one of the world's leading biotechnology companies, reaching over 10 million patients worldwide. Become the professional you are meant to be in this meaningful role. Senior Associate, Physical Security Systems Live What you will do Let's do this. Let's change the world. In this vital role you will be responsible for overseeing daily global operations regarding all security technology systems and hardware along with the planning of the physical security systems and service requirements for the Global Enterprise. Primary duties may include, but are not limited to: * Programs security clearance codes, develops tests and identifies system irregularities. Processes System Access Report requests for the multiple sites. * Partners with all stakeholders in the definition of physical security system standards, required upgrades, maintenance, and the day-to-day operation of all security systems through system integrators or internal resources. * Analyzes the viability and functionality of security systems, legacy and new, business disruption as the result of failed or improperly configured systems. * Develops and implements recommended improvements that involve technology solutions aligned with corporate security goals and budget guidelines. * Maintains an in-depth knowledge of the state-of-the-art security equipment standards and technology encompassing all physical security products. * Recommends system solutions to specific security concerns identified through customer requests, security audits and management. * Performs operational processes to ensure security standards are maintained. Administers processes for annual audits for various access control systems for all countries * Provides product research, feasibility studies, project planning, tracking and quality assurance and overall vendor communication and management. * Provides systems reports and evidence as necessary to support investigations conducted by Global Security & Safety, HR and Financial Investigations. * Knowledge of security systems (hardware and software) utilized by Amgen, including - Access control, CCTV, Visitor management systems, Incident Reporting, Key Systems, Alarm systems. * Recognizes and escalates problems that may arise regarding company security systems * Applies knowledge and understanding of customer needs and other internal/external contacts * Establishes working relationships with other key stakeholders * Works under general direction of senior systems' personnel within the department Win What we expect of you We are all different, yet we all use our unique contributions to serve patients. The systems administration professional we seek is a senior associate with these qualifications. Basic Qualifications Master's degree Or Bachelor's degree and 2 years of Computer Science experience Or Associate's degree and 6 years of Computer Science experience Or High school diploma / GED and 8 years of Computer Science experience Preferred Qualifications * Strong Microsoft Office skills. * Good understanding of TCP/IP network architecture. * Good communication and decision-making skills * Ability to work independently with minimal supervision * Ability to work effectively with external business partners and contractors. Thrive What you can expect of us As we work to develop treatments that take care of others, we also work to care for our teammates' professional and personal growth and well-being. The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications. Amgen offers a Total Rewards Plan comprising health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities including: * Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts. * A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan * Stock-based long-term incentives * Award-winning time-off plans and bi-annual company-wide shutdowns * Flexible work models, including remote work arrangements, where possible Apply now for a career that defies imagination Objects in your future are closer than they appear. Join us. careers.amgen.com Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. Apply Now

**Join Amgen's Mission of Serving Patients** At Amgen, if you feel like you're part of something bigger, it's because you are. Our shared mission-to serve patients living with serious illnesses-drives all that we do. Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest diseases. With our focus on four therapeutic areas -Oncology, Inflammation, General Medicine, and Rare Disease- we reach millions of patients each year. As a member of the Amgen team, you'll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you'll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career. **Commercial Programs Quality Oversight and Monitoring lead** **What you will do** Let's do this. Let's change the world. In this vital role you will provide quality oversight for Patient Support Programs, Market Research, Digital Health, Websites and Social Media working closely with Commercial and Medical. The lead of Commercial Programs and Monitoring Quality will provide guidance to Amgen senior stakeholders including Commercial, Global Patient Safety, Regulatory Affairs and Operations to identify and resolve Quality issues and mitigate compliance risk. They will provide expert advice on Pharmacovigilance programs, initiatives, and activities to help manage and mitigate risk and to build in quality at the rime of process creation. Report and increase significant compliance issues to R&D Quality management and senior collaborators. Ensure proactive identification, customer concern, management, and remediation of compliance issues relating to Amgen processes, programs, and external relationships. **Responsibilities:** + Line Manager of professional staff in the range of 2 to 4 individuals. + Development and conduct of the annual audit program for Patient Support Programs, Market Research, Digital Health, Websites and Social Media. + Lead Audits and Monitoring Visits (External Engagement) and staff across Quality teams for all Amgen Products. + Facilitate and review responses to inspections, audits and monitoring visits, with timely and appropriate remediation of audit and inspection findings. + Advance Risk Based thinking, Proactive Quality Management and Quality by Design, including the following core activities: Audit Management Contract Review and Negotiation, Vendor Oversight, Inspection Preparation, Management, & Execution, eviation/ CAPA Management, and Privacy Issues. + Serve as the PV representative on senior compliance/ quality oversight bodies. E.g., Safety Reporting for Commercial Programs (SRCP). + Understands impact of emerging regulatory trends and their implications for Amgen + Analyzes and forecasts regulatory trends. + Develops complex solutions to problems through in-depth analysis, coordination, and negotiation with key decision makers. + Adapts and integrates own experience with Amgen-wide strategy. + Participates in Industry forums designed to benchmark and continuously improve in the areas of GPvP Quality Management. + Lead the Deviations process in the Safety & Medical Quality team as part of the implementation of Amgen's new Quality management system. **What we expect of you** We are all different, yet we all use our unique contributions to serve patients. The professional we seek is a leader with these qualifications. **Basic Qualifications:** Doctorate degree and 3 years of R&D, Operations and/or Quality experience in the PhRMA/Biotech sector **Or** Master's degree and 7 years of R&D, Operations and/or Quality experience in the PhRMA/Biotech sector **Or** Bachelor's degree and 9 years of R&D, Operations and/or Quality experience in the PhRMA/Biotech sector **Or** Associate's degree and 12 years of R&D, Operations and/or Quality experience in the PhRMA/Biotech sector **Or** High school diploma / GED and 14 years of R&D, Operations and/or Quality experience in the PhRMA/Biotech sector In addition to meeting at least one of the above requirements, you must have a minimum of 3 years experience directly managing people and/or leadership experience leading teams, projects, programs, or directing the allocation or resources. Your managerial experience may run concurrently with the required technical experience referenced above **Preferred Qualifications:** + Experience managing GPvP Quality Management including motivating change across functions. + Demonstrated track record leading impactful teams within the biotechnology and/or pharmaceutical industry. + Understanding of the legal and regulatory environment affecting PhRMA/Biotech + Ability to create, grow, and develop high-performing teams that deliver outstanding business results. + Experience fostering an environment that drives creativity and innovation. + Ability to operate independently in a strategic and tactical manner and ability to work through ambiguity across GPvP in designing and implementing learning and training solutions. + Ability to partner effectively with collaborators at senior and junior levels and develop broad-based solutions designed to meet a variety of organizational and business needs. + Exceptional oral and written communication and writing skills. **What you can expect of us** As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we'll support your journey every step of the way. The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications. In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include: + A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts + A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan + Stock-based long-term incentives + Award-winning time-off plans + Flexible work models, including remote and hybrid work arrangements, where possible **Apply now** **for a career that defies imagination** Objects in your future are closer than they appear. Join us. **careers.amgen.com** In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information. **Application deadline** Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position. As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease. Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

**HOW MIGHT YOU DEFY IMAGINATION?** You've worked hard to become the professional you are today and are now ready to take the next step in your career. How will you put your skills, experience and passion to work toward your goals? At Amgen, our shared mission-to serve patients-drives all that we do. It is key to our becoming one of the world's leading biotechnology companies, reaching over 10 million patients worldwide. Come do your best work alongside other innovative, driven professionals in this meaningful role. Scientist - Biochemistry & Pharmacology **Live** **What you will do** Let's do this. Let's change the world. Amgen is seeking a talented and motivated individual with expertise in biochemical & cell-based assay development in support of Amgen's small molecule drug discovery pipeline. In this vital role you will be responsible for designing, developing, and optimizing assays to identify and validate potential drug candidates, including reversible inhibitors, covalent inhibitors, and degraders. The successful candidate should possess strong technical expertise & laboratory skills, have excellent written and oral communication skills, work productively in a collaborative cross-functional team environment, and keep current with field of expertise, including literature and technology development + Develop and optimize biochemical assays to support HTS, hits validation, and lead optimization for novel therapeutic targets + Develop and execute cell-based assays to assess the effects of small molecules on cellular pathways, receptor activity, and phenotypic outcomes + Apply sophisticated bioassay techniques to develop and perform potency, kinetic and mechanistic assays for hits validation, compound-target engagement, and SAR study + Evaluate and implement new technologies to enhance screen capabilities and assay performance + Stay current with scientific literature and industry trends related to assay technologies, novel drug modalities, and drug discovery + Represent department in multi-disciplinary project teams to present research results and provide scientific and technical support + Collaborate with internal cross-functional teams and external partners to enable project progression **Win** **What we expect of you** We are all different, yet we all use our unique contributions to serve patients. The professional we seek is a motivated scientist with these qualifications. **Basic Qualifications:** Doctorate & relevant scientific experience **OR** Master's degree & 2 years of scientific experience **Preferred Qualifications:** + PhD in Biochemistry, Pharmacology, Cell Biology, Molecular Biology or a related field, with relevant postdoctoral experience preferred + Expertise in quantitative pharmacology, enzymology, and ligand binding kinetics. + Small molecule drug discovery experience in novel modalities including but not limited to reversible inhibitors, covalent inhibitors, or degraders. + A deep and broad understanding of the development, validation & execution of a wide array of binding & functional activity-based assays such as AlphaScreen, TR-FRET, FP, etc. + Demonstrated ability to develop and implement cellular assays for target validation, hit identification, and lead optimization, such as MesoScale Discovery, HiBIT, NanoBRET, and cell reporter assays + Highly skilled in the development & implementation of robust, automated, 384 or 1536-well plate-based assays using a wide range of detection methods (e.g., spectrophotometry, radiometry, luminescence, fluorescence) + Experience with microplate readers and automated liquid handling systems (e.g., PerkinElmer Envision, Labcyte Echo, Agilent Bravo, etc.) + Experience with data analysis and visualization software platforms (e.g., Genedata Screener, Tibco Spotfire, GraphPad Prism, etc.) + Excellent organizational, interpersonal and communication skills, along with the ability to work in a flexible team-oriented environment **Thrive** **What you can expect of us** As we work to develop treatments that take care of others, we also work to care for our teammates' professional and personal growth and well-being. The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications. Amgen offers a Total Rewards Plan comprising health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities including: + Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts. + A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan + Stock-based long-term incentives + Award-winning time-off plans and bi-annual company-wide shutdowns + Flexible work models, including remote work arrangements, where possible **Apply now** **for a career that defies imagination** Objects in your future are closer than they appear. Join us. **careers.amgen.com** **Application deadline** Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position. Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

**Join Amgen's Mission of Serving Patients** At Amgen, if you feel like you're part of something bigger, it's because you are. Our shared mission-to serve patients living with serious illnesses-drives all that we do. Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest diseases. With our focus on four therapeutic areas -Oncology, Inflammation, General Medicine, and Rare Disease- we reach millions of patients each year. As a member of the Amgen team, you'll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you'll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career. **Supply Chain Senior Manager - Global Supply Chain Leader** **What you will do** Let's do this. Let's change the world. In this pivotal role, you will report to the Planning Lead within the Global Supply Chain Organization and will be accountable to deliver strong and agile product leadership through the orchestration of end-to-end global Supply Chain strategies that ensure efficient and reliable patient supply. With the end-to-end supply chain oversight of products, the Senior Manager will be responsible for establishing supply chain resolutions to mitigate against threats to the continuity of supply and advise Executive Management on short and long-term decision making. The Senior Manager will also work with site and regional planners to ensure Amgen's manufacturing network supply plans. **Responsibilities:** **Strategy** + Primary focus is to provide thought leadership in orchestrating the LRS and Planning cycles, make decisions on business-critical Life cycle management and implementation of product strategies. + Ensure every patient every time by driving supply risk mitigation strategies to ensure supply continuity with engagement from a wide matrixed team (through PDT, Mfg Sites and commercial) + Represents Global, regional and site Supply Chain in the PDT and advice PDT on added customer value of strategic LCM initiatives. + Provide supply chain thought leadership to Supply Chain Management and OSBR office for Siting Assessments, Network Evaluation and a plethora of cases to ensure supply; As a critical business partner, responsible to develop demand & supply strategies to influence supply chain design. + Shares and develops standard processes across the Global Supply Chain network through the support of network initiatives to drive improvements in Supply Chain processes, systems, and procedures. + Interfaces across functions including Supply Chain, Manufacturing, Finance, Regulatory, and Quality at various level of detail, to advice and highlight issues and options to Senior Leadership Team. **Execution** + Accountable for supervising the operational and tactical commercial supply planning performance, using appropriate key performance indicators. + Provides guidance and technical advice on global supply chain processes and systems. + Responsible for full Value Stream Mapping of all commercial products including lead-time, critical raw materials, capacity. + Responsible to drive discussions with Mfg Sites, GNP and Finance to set inventory guardrails and ensure working capital goals are realized with adherence to DIO targets. + Understand COGM/COS to drive supply chain allocation discussions to enable revenue growth and supply for price sensitive markets. + Lead and support special initiatives within the Global Supply Chain such as acquisitions, mergers, transformation to enable continued growth of Amgen **What we expect of you** We are all different, yet we all use our unique contributions to serve patients. The supply chain professional we seek is a leader with these qualifications. **Basic Qualifications:** Doctorate degree and 2 years of Supply Chain, or Operations experience **Or** Master's degree and 4 years of Supply Chain, or Operations experience **Or** Bachelor's degree and 6 years of Supply Chain, or Operations experience **Or** Associate's degree and 10 years of [Supply Chain, or Operations experience **Or** High school diploma / GED and 12 years of Supply Chain, or Operations experience **Preferred Qualifications:** + Knowledge and experience in applying advanced planning techniques as it relates to demand, supply, inventory planning, financials, and Mfg. network planning. + Excellent communication capabilities and must be comfortable and confident dealing with all levels of management within the organization. + 7 plus years of experience in global pharmaceutical, biotech or any other industry + Solid understanding of demand/supply planning, Supply Chain principles and logistics + Ability to perform system-based advanced supply planning and scenario analysis + Diligent with strong business analytical skills and company-wide knowledge + Process-oriented mentality with leadership experience to identify gaps and seek solutions + Perseverance and independent problem-solving skills + Knowledge and understanding of COGM, COGS and NPV analyses **What you can expect of us** As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we'll support your journey every step of the way. The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications. In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include: + A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts + A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan + Stock-based long-term incentives + Award-winning time-off plans + Flexible work models, including remote and hybrid work arrangements, where possible **Apply now** **for a career that defies imagination** Objects in your future are closer than they appear. Join us. **careers.amgen.com** In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information. **Application deadline** Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position. As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease. Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

Career CategoryClinicalJob DescriptionJoin Amgen's Mission of Serving Patients At Amgen, if you feel like you're part of something bigger, it's because you are. Our shared mission-to serve patients living with serious illnesses-drives all that we do. Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest diseases. With our focus on four therapeutic areas -Oncology, Inflammation, General Medicine, and Rare Disease- we reach millions of patients each year. As a member of the Amgen team, you'll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you'll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career. Director Clinical Program Resource Management What you will do Let's do this. Let's change the world. In this vital role you will oversee and manage global Clinical Program Operations (CPO) resources and Functional Service Provider (FSP) performance. The role includes translating business strategy into effective resource planning, supporting standardization and efficiency, driving continuous improvement initiatives within the CPO function and its interactions with Global Development Operations (GDO) function. Recruitment, line management, performance management and mentoring of Program Research Management (PRM) staff Global-level functional oversight of the CPO roles (e.g. Global Trial Manager, Local Trial Manager) Coordinate FSP performance and resource allocation Lead strategic staff-focused process improvement and training initiatives Contribute to risk assessment and mitigation Partner with stakeholders and external suppliers Support CPO goal setting, drive operational efficiency and onboarding What we expect of you We are all different, yet we all use our unique contributions to serve patients. The professional we seek is experienced with these qualifications. Basic Qualifications: Doctorate degree and 4 years of related experience Or Master's degree and 7 years of related experience Or Bachelor's degree and 9 years of related experience Preferred Qualifications: Experience in life sciences or medical field, including biopharmaceutical clinical research with a sophisticated knowledge of global clinical trial management and ICH/GCP regulations Previous managerial/leadership experience and oversight of clinical research vendors Project, program and resource management skills as well as organizational capacity Time, cost and quality metrics Experience in developing goals and training plans for staff development What you can expect of us As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we'll support your journey every step of the way. The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications. In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include: A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan Stock-based long-term incentives Award-winning time-off plans Flexible work models, including remote and hybrid work arrangements, where possible Apply now for a career that defies imagination Objects in your future are closer than they appear. Join us. careers.amgen.com In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information. Application deadline Amgen anticipates accepting applications until March 11, 2025; however, we may continue accepting applications beyond this date if we do not receive a sufficient number of candidates. As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease. Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. . Salary Range 199,677.00 USD - 232,895.00 USD

**HOW MIGHT YOU DEFY IMAGINATION?** If you feel like you're part of something bigger, it's because you are. At Amgen, our shared mission-to serve patients-drives all that we do. It is key to our becoming one of the world's leading biotechnology companies. We are global collaborators who achieve together-researching, manufacturing, and delivering ever-better products that reach over 10 million patients worldwide. It's time for a career you can be proud of. **Clinical Research Sr Medical Scientist, Endocrinology - US, Remote** **Live** **What you will do** Let's do this. Let's change the world. In this vital role you will support the design, assessment, and communication of clinical programs which support the global scientific/medical evidence plan. + Support cross-functional and global collaborations to integrate broad medical, scientific, and commercial input into the clinical development program. Participate and provide clinical input into safety and regulatory interactions. + Provide clinical/scientific input during the development and execution clinical trials. + Review data from clinical trials related to medical monitoring, as well as support and address questions from sites and from investigators. + As needed, provide clinical/scientific input into, author sections of, and QC study-related documents (e.g. study concept documents and protocols). Interpret clinical trial data and participate in safety assessments. Review and provide clinical scientific input to safety narratives. Initiate database analyses to support commercial/clinical objectives. + Contribute to the preparation of clinical study reports and regulatory submissions. + Support interactions with regulatory agencies if needed. + Develop key opinion leaders and make scientific presentation at advisory boards, key scientific meetings and external committee meetings as delegated by the GDL or delegee and help identify new clinical research opportunities. **Win** **What we expect of you** We are all different, yet we all use our unique contributions to serve patients. The dynamic professional we seek is a leader with these qualifications: **Basic Qualifications:** Doctorate degree and 2 years of experience in clinical trials implementation in obesity, diabetes, or metabolic diseases OR Master's degree and 4 years of experience in clinical trials implementation in in obesity, diabetes, or metabolic diseases OR Bachelor's degree and 6 years of experience in in clinical trials implementation in obesity, diabetes, or metabolic diseases OR Associate's degree and 10 years of experience in clinical trials implementation in obesity, diabetes, or metabolic diseases **Preferred Qualifications:** + Accredited residency in Endocrinology, board certified or equivalent 2+ years of clinical research experience and/or basic science research combined with clinical teaching and patient care activities + MD preferred. + Prior research in obesity, diabetes, or metabolic diseases preferred. + An understanding of the scientific method and clinical applications based medical, scientific and practical rationale + Familiarity with concepts of clinical research and clinical trial design and execution including biostatistics + Familiarity with regulatory agency organization, guidelines, and practices + Ability to effectively present ideas and document complex medical/clinical concepts in both written and oral communication History of solving problems, especially in implementation of clinical trials while exhibiting superior judgment and balanced, realistic understanding of issues. **Thrive** **What you can expect of us** As we work to develop treatments that take care of others, we also work to care for our teammates' professional and personal growth and well-being. The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is $168,677. to $218,907. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications. Amgen offers a Total Rewards Plan comprising health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities including: + Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts. + A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan + Stock-based long-term incentives + Award-winning time-off plans and bi-annual company-wide shutdowns + Flexible work models, including remote work arrangements, where possible **Apply now** **for a career that defies imagination** Objects in your future are closer than they appear. Join us. **careers.amgen.com** Application deadline Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position. Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. \#obesity

HOW MIGHT YOU DEFY IMAGINATION? You've worked hard to become the professional you are today and are now ready to take the next step in your career. How will you put your skills, experience and passion to work toward your goals? At Amgen, our shared mission-to serve patients-drives all that we do. It is key to our becoming one of the world's leading biotechnology companies, reaching over 10 million patients worldwide. Come do your best work alongside other innovative, driven professionals in this meaningful role. Associate Manufacturing I - Days Live What you will do Let's do this! Let's change the world! In this vital role you will perform operations in the Manufacturing area. Operations will be performed according to Standard Operating Procedures (SOPs), these can include bioreactor cleaning, steaming, inoculation, etc., operations. Perform and monitor critical processes, complete routine validation protocols, and regularly draft and revise documents such as Manufacturing Procedures, SOPs, and technical reports. Perform basic troubleshooting and assist in the review of documentation for assigned functions. Participate on cross-functional teams and represent the manufacturing teams. May also have the responsibility of owning deviations/CAPAs. Identify, recommend, and implement improvements related to routine functions. This position is for the AR5 A shift Upstream Cell Culture (Perfusion, Production, Harvest - PPH) team. The successful candidate will be expected to join a shift team working a 12-hour shift. The shift pattern will be 7AM-7PM with a two-week rotation covering 7 days per week. The rotating shift offers several benefits, with an average of 14 days on shift per month with every other weekend off. In addition, any Sundays worked receive Premium pay. Qualifications Win What we expect of you We are all different, yet we all use our unique contributions to serve patients. The dedicated professional we seek is an excellent teammate with these qualifications. Basic Qualifications: High school/GED + 2 years of manufacturing or operations work or military experience OR Associate's + 6 months of manufacturing or operations work or military experience Preferred Qualifications: Bachelor's degree in Science or Engineering Knowledge of large-scale biotechnology operations such as purification, cell culture, aseptic processing, etc. Knowledge of Single-use-Systems CFR and Regulatory knowledge Mechanical ability/expertise Basic statistical mathematical skills Ability to interpret and apply GMP knowledge Understanding of analytical methods for manufacturing area Demonstrated technical writing capability Able to demonstrate project management skills and presentation skills Ability to understand, apply and evaluate basic chemistry, biology and physical principles Basic troubleshooting skills on production equipment Experience with Delta V Experience with lab equipment/testing Additional Information Thrive What you can expect of us As we work to develop treatments that take care of others, we also work to care for our teammates' professional and personal growth and well-being. The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications. Amgen offers a Total Rewards Plan comprising health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities including: Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts. A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan Stock-based long-term incentives Award-winning time-off plans and bi-annual company-wide shutdowns Flexible work models, including remote work arrangements, where possible Apply now for a career that defies imagination Objects in your future are closer than they appear. Join us. careers.amgen.com Application deadline Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position. Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. All your information will be kept confidential according to EEO guidelines.

At STERIS, we help our Customers create a healthier and safer world by providing innovative healthcare and life science product and service solutions around the globe. You do not have to have previous instrument repair experience to be considered. This is an entry level job - we will train you! Transferable experience may include hands-on repair, assembly, product testing, small engine repair, cell phone and electronics repair/ testing/ re-builds, carpentry, circuit board assembly/repair, industrial sewing, jewelry repair, maintenance, construction, and automotive repair. In this position, you will perform surgical instrument inspection, repair, and refurbishment in a field-based setting. Technicians work out of mobile repair trucks at Customer sites and regional labs in more condensed markets. Technicians deliver superior Customer Experience by providing timely and quality repairs to meet compliance standards. This position may require occasional overnight travel. This role requires daily travel by driving a company vehicle. If offered this position, STERIS will run a 7 year driving record check, as part of our onboarding process. Click this video to take a peek at the truck and the work you could be doing to help STERIS create a safer, healthier world! This is a remote based customer facing position. To support and service our customers in this assigned territory candidates must be based out of Vermont or New York state (within reasonable commuting distance of Burlington). What you'll do as a Repair Technician: * Perform basic to intermediate inspection and repairs on surgical instrumentation using grinding wheels, buffing wheels, various hand and power tools, soldering, etc. Complexity of repairs and level of intricacy will vary. * You will work in the field on a mobile repair truck, inside a repair lab or inside a hospital, based on the needs of the Customer within the assigned territory. * Provide invoicing and documentation based on business need. * Provide support various locations within assigned territory depending on the service agreements, Customer needs, and staffing levels. The Experience, Skills, and Abilities Needed: Required: * High school diploma or GED required * 2+ years of work experience, including at least 1 year of relevant experience*, or 1 year of experience at STERIS. All experience must be verifiable. * Must be able to meet flexible schedules with early/late hours and occasional overnight/out of state travel, based on Customer and business needs. * Must be able to pass a DOT medical/ physical exam, comply with all DOT regulations and conduct basic box truck safety checks. * Must have a valid driver's license with an acceptable driving record (CDL not required). * Must be at least 21 years old to meet the FMCSA age requirement for commercial interstate driving. * Must be able to lift up to 25 pounds at times and push instrument carts ranging from 10-150 pounds at times. * Must be able to be compliant with hospital/Customer credentialing requirements Other: * What is relevant work experience? Hands-on repair, assembly, or product testing, and use of small hand tools is a plus. Examples of relevant work experience or transferrable skills are small engine repair, cell phone/ electronics repair, testing, re-builds, carpentry, circuit board assembly/ repair, industrial sewing, maintenance, construction, welding, fabrication, automotive repair, and jewelry repair. What STERIS Offers: We value our employees and are committed to providing a comprehensive benefits package that supports your health, well-being and financial future. Here is a brief overview of what we offer: * Extensive hands-on training and development * Career progression path with STERIS Instrument Management Services and growth opportunities in other parts of STERIS * Competitive pay * Overtime opportunity * Annual merit review and incentive plans * Uniforms and all necessary tools provided * Business travel and all related expenses paid * Medical, vision, prescription, dental and life insurance * 401(k) with a company match * Paid time off that accrues from day one and paid holidays * Tuition assistance * Opportunities for advancement IND123 #LI-AC1 Pay range for this opportunity is $22/hour - $24/hour. Minimum pay rates offered will comply with county/city minimums, if higher than range listed. Pay rates are based on a number of factors, including but not limited to local labor market costs, years of relevant experience, education, professional certifications, foreign language fluency, etc. Employees (and their families) may enroll in our company-sponsored medical, dental, vision, flexible spending, health savings account, voluntary benefits, supplemental life/AD&D plans and the company's 401k plan. Employees are covered by an employee assistance program (also available to household members) and long-term disability. Full-Time Employees are also eligible for short-term disability. Full-time Employees will also receive Paid Time Off (PTO) based on years of service and paid Holidays. Part-time employees working 20 or more hours receive a pro-ration of the full-time PTO allocation and paid Holidays based on their standard hourly work week. Full-Time employees are eligible for four weeks of paid parental leave. Part-time employees also receive paid parental leave, pro-rated based on their standard hourly work week. STERIS is an Equal Opportunity Employer. We are committed to equal employment opportunity and the use of affirmative action programs to ensure that persons are recruited, hired, trained, transferred and promoted in all job groups regardless of race, color, religion, age, disability, national origin, citizenship status, military or veteran status, sex (including pregnancy, childbirth and related medical conditions), sexual orientation, gender identity, genetic information, and any other category protected by federal, state or local law. We are not only committed to this policy by our status as a federal government contractor, but also we are strongly bound by the principle of equal employment opportunity. Req ID: 46884 Job Category: Service/Technical Services Location: Burlington, VT, US, 05401 Workplace Type: Remote Life at STERIS STERIS Sustainability

LOCATIONS: US - California - South San Francisco WORK LOCATION TYPE: Flex Commuter / Hybrid DATE POSTED: Apr. 23, 2024 CATEGORY: Business Development SALARY RANGE: 194,497.00 USD - 230,061.00 USD HOW MIGHT YOU DEFY IMAGINATION? If you feel like you're part of something bigger, it's because you are. At Amgen, our shared mission-to serve patients-drives all that we do. It is key to our becoming one of the world's leading biotechnology companies. We are global collaborators who achieve together-researching, manufacturing, and delivering ever-better products that reach over 10 million patients worldwide. It's time for a career you can be proud of. Director of External Research & Development Live What you will do Let's do this! Let's change the world. In this vital role within the External R&D group of Business Development you will be part of a team responsible for leading Amgen's business development efforts in identifying and evaluating innovative therapeutics being developed outside of Amgen within the Inflammation/autoimmune therapeutic space for potential in-licensing, M&A, or collaborations. The successful candidate will develop and nurture a network of key industry and academic contacts to ensure robust communication of ideas, interests and information between the external community and internal groups. The role requires proactive efforts to manage the search and identification of opportunities through networking and reviews of the external landscape and assessing prioritizing based on Amgen's therapeutic area strategy. The role includes leading the technical evaluations of opportunities by creating and managing cross-functional review teams, providing recommendations based on robust scientific and drug industry knowledge, and ensuring appropriate and efficient decision-making processes. This person will ensure efficient reviews and engage in business negotiations and work with legal to execute contractual agreements for certain projects. The candidate will be responsible for leading strategic discussions and presentations, collaborating closely with senior management, R&D, and Commercial to develop a set of priorities for licensure or M&A. This person will also be expected to successfully mentor any direct reports and present themselves as a thoughtful and respected professional to both internal colleagues and external parties. The role will also include the support of out-licensing activities. It is highly preferred that this role be located at an Amgen Research hub in either South San Francisco, CA or Thousand Oaks, CA or other remote location in the Pacific Time zone to match most of our research teams. Win What we expect of you We are all different, yet we all use our unique contributions to serve patients. The professional we seek will have the following qualifications. Basic Qualifications: Doctorate degree in a scientific field & 4 years of experience in drug development industry and/or biopharma business development Or Master's degree in a scientific field & 7 years of experience in drug development industry and/or biopharma business development Or Bachelor's degree in a scientific field & 9 years of experience in R&D and/or biopharma business development Preferred Qualifications: * Doctorate in scientific discipline, with robust working knowledge in inflammation, oncology or other therapeutic area. * 4+ years of management and/or leadership experience in business and drug development activities, and strong technical R&D experience along with business development and licensing experience. * Strong leadership, scientific, organizational, communication, and project management skills and ability to manage multiple projects simultaneously. * Excellent presentation skills. Effective communication skills pertaining to scientific and business development. Must demonstrate ability to foresee and solve problems, and prioritize and meet deadlines. Strong team player, experience in successfully managing direct reports and a demonstrated ability to interface effectively with all-levels of staff across differing functional expertise. * Demonstrated ability to create and build relationships with internal and external parties. * Professional demeanor with strong decision making * Be able to work independently, manage large cross functional teams, and mentor individuals. Thrive What you can expect of us As we work to develop treatments that take care of others, we also work to care for our teammates' professional and personal growth and well-being. In addition to the base salary, Amgen offers a Total Rewards Plan comprising health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities including: * Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts. * A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan * Stock-based long-term incentives * Award-winning time-off plans and bi-annual company-wide shutdowns * Flexible work models, including remote work arrangements, where possible Apply now for a career that defies imagination In our quest to serve patients above all else, Amgen is the first to imagine, and the last to doubt. Join us. careers.amgen.com Application deadline Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position. Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. #CLOLI Apply Now