Project Manager Jobs at Amgen with Visa Sponsorship
Project Manager jobs at Amgen sit at the intersection of science, operations, and cross-functional leadership, spanning drug development, clinical programs, and manufacturing. Amgen has a strong track record of sponsoring international talent across multiple visa categories for this function, making it a realistic target for foreign nationals building a career in biotech.
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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.
Senior Associate Manufacturing - Continuous Improvement Lead
What You Will Do
Let’s do this. Let’s change the world. In this vital role you will have the outstanding opportunity to support the start-up of the Amgen North Carolina (ANC) manufacturing facility. During start up, the Manufacturing Senior Associate Continuous Improvement (CI) Leads will have ownership and oversight of operational readiness activities in manufacturing areas such as: Dispensing, Buffer/Media Preparation, Upstream Cell Culture, Harvest, Downstream Purification, Analytical Testing, or Column Packing. CI leads will support Standard Operating Procedure (SOP) creation, review, and approval; specification and purchasing of required equipment and supplies, design of job aids and work instructions, advancement of digital tools to support manufacturing operations, and training of staff. When the plant transitions to operations in 2025 this position will manage and lead the CI program for MFG.
- Provide technical support and subject matter expertise for manufacturing area.
- Oversee support and ongoing development of all the manufacturing systems including SOP, TRNQ, MES, QMS records, among others.
- Train staff (associates, operators, technical/QA/support) on assigned manufacturing systems.
- Support troubleshooting needs during commissioning/qualification, start-up, engineering run, and process performance qualification of the ANC manufacturing facility.
- Facilitate process, area, and equipment quality risk assessments as needed to identify risks, failure modes, and mitigating actions.
- When the plant is in production, manage the CI program; this includes conducting time studies to identify process inefficiencies, leading improvement projects in designated MFG area (i.e. upstream, downstream, solution prep), implementing proper change management, and tracking sustainment of implemented changes.
- Lead cross-functional CAPAs and EVs as required.
- Serve as a CI and Human and Organizational Performance champion. Provide training to others on CI and lean principles.
- Lead learning team meetings and kaizen events.
What We Expect Of You
We are all different, yet we all use our unique contributions to serve patients. The professional we seek will possess strong project management and innovative thinking as well as these qualifications.
Basic Qualifications:
- High school diploma / GED and 4 years of Manufacturing or Operations experience OR
- Associate’s degree and 2 years of Manufacturing or Operations experience OR
- Bachelor’s degree and 6 months of Manufacturing or Operations experience
- Masters degree
Preferred Qualifications:
- Educational background in Life Sciences, Chemistry, Biochemistry, Industrial Biotechnology, and/or Engineering
- Strong technical knowledge of drug substance processing (cell culture, harvest, chromatography, filtration, buffer compounding) and a broad understanding of related disciplinary areas in bioprocessing
- Proficient technical writing and presentation skills so as to communicate complex information effectively with technical and senior management staff
- Ability to lead small and large cross-functional meetings efficiently.
- Knowledge of process improvement or lean fundamentals.
- Collaborate with staff at all levels in the organization, including technical and management staff within manufacturing, process development, engineering, supply chain, and quality
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. In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards. Apply now and make a lasting impact with the Amgen team.
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.
Job Description
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.
Senior Associate Manufacturing - Continuous Improvement Lead
What You Will Do
Let’s do this. Let’s change the world. In this vital role you will have the outstanding opportunity to support the start-up of the Amgen North Carolina (ANC) manufacturing facility. During start up, the Manufacturing Senior Associate Continuous Improvement (CI) Leads will have ownership and oversight of operational readiness activities in manufacturing areas such as: Dispensing, Buffer/Media Preparation, Upstream Cell Culture, Harvest, Downstream Purification, Analytical Testing, or Column Packing. CI leads will support Standard Operating Procedure (SOP) creation, review, and approval; specification and purchasing of required equipment and supplies, design of job aids and work instructions, advancement of digital tools to support manufacturing operations, and training of staff. When the plant transitions to operations in 2025 this position will manage and lead the CI program for MFG.
- Provide technical support and subject matter expertise for manufacturing area.
- Oversee support and ongoing development of all the manufacturing systems including SOP, TRNQ, MES, QMS records, among others.
- Train staff (associates, operators, technical/QA/support) on assigned manufacturing systems.
- Support troubleshooting needs during commissioning/qualification, start-up, engineering run, and process performance qualification of the ANC manufacturing facility.
- Facilitate process, area, and equipment quality risk assessments as needed to identify risks, failure modes, and mitigating actions.
- When the plant is in production, manage the CI program; this includes conducting time studies to identify process inefficiencies, leading improvement projects in designated MFG area (i.e. upstream, downstream, solution prep), implementing proper change management, and tracking sustainment of implemented changes.
- Lead cross-functional CAPAs and EVs as required.
- Serve as a CI and Human and Organizational Performance champion. Provide training to others on CI and lean principles.
- Lead learning team meetings and kaizen events.
What We Expect Of You
We are all different, yet we all use our unique contributions to serve patients. The professional we seek will possess strong project management and innovative thinking as well as these qualifications.
Basic Qualifications:
- High school diploma / GED and 4 years of Manufacturing or Operations experience OR
- Associate’s degree and 2 years of Manufacturing or Operations experience OR
- Bachelor’s degree and 6 months of Manufacturing or Operations experience
- Masters degree
Preferred Qualifications:
- Educational background in Life Sciences, Chemistry, Biochemistry, Industrial Biotechnology, and/or Engineering
- Strong technical knowledge of drug substance processing (cell culture, harvest, chromatography, filtration, buffer compounding) and a broad understanding of related disciplinary areas in bioprocessing
- Proficient technical writing and presentation skills so as to communicate complex information effectively with technical and senior management staff
- Ability to lead small and large cross-functional meetings efficiently.
- Knowledge of process improvement or lean fundamentals.
- Collaborate with staff at all levels in the organization, including technical and management staff within manufacturing, process development, engineering, supply chain, and quality
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. In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards. Apply now and make a lasting impact with the Amgen team.
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.
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Get Access To All JobsTips for Finding Project Manager Jobs at Amgen
Frame your PM credentials around biotech pipelines
Amgen's Project Manager roles typically require experience coordinating cross-functional teams in regulated environments. Before applying, align your resume to drug development lifecycles, IND or NDA milestones, or GxP-compliant workflows so your background reads as directly transferable.
Target roles tied to active therapeutic programs
Amgen regularly staffs Project Managers against specific pipeline assets in oncology, inflammation, and rare disease. Filtering open roles by therapeutic area helps you identify postings with the most urgency and the clearest sponsorship path rather than generalist requisitions.
Use Migrate Mate to surface sponsorship-verified PM openings
Not every Project Manager posting at Amgen explicitly states visa sponsorship. Migrate Mate filters roles by confirmed sponsorship history for this function, so you can focus your applications on postings where international candidates have a documented track record of success.
Clarify your visa type early in recruiter conversations
Amgen's talent acquisition team handles a range of visa categories, so be specific: if you're on F-1 OPT, state your OPT end date and STEM extension eligibility upfront. Recruiters need this to route your file correctly before an offer is extended.
Prepare for the LCA wage and location specifics at filing
For H-1B or E-3 sponsorship, your employer files a Labor Condition Application with the DOL certifying your wage meets the prevailing level for your work location. If your role spans multiple Amgen sites, confirm the primary worksite with HR before the LCA is submitted to avoid amendments later.
Align your PMP or equivalent certification before the offer stage
Many of Amgen's Project Manager postings list PMP certification or a science-related degree as a baseline. Having both on your resume before interviews removes a common objection that can slow down or complicate sponsorship approval at the offer stage.
Frequently Asked Questions
Does Amgen sponsor H-1B visas for Project Managers?
Yes, Amgen sponsors H-1B visas for Project Manager roles. The company has a consistent pattern of filing H-1B petitions for this function across its U.S. locations, including sites in California, Washington, and Massachusetts. Because H-1B sponsorship depends on the annual lottery, Amgen also supports other visa categories so international candidates aren't solely dependent on H-1B selection.
How do I apply for Project Manager jobs at Amgen?
Apply directly through Amgen's careers portal, where Project Manager roles are posted by therapeutic area, site, and seniority level. Before applying, confirm that the posting is open to visa sponsorship, since not every requisition states this explicitly. Migrate Mate surfaces Amgen's Project Manager openings filtered by sponsorship history, which helps you prioritize roles where international hires have been supported before.
Which visa types does Amgen commonly sponsor for Project Manager roles?
Amgen sponsors several visa categories for Project Managers, including H-1B, E-3 visa for Australian nationals, TN visa for Canadian and Mexican nationals, and F-1 OPT and CPT for students in qualifying degree programs. For candidates on a longer-term path, Amgen also supports EB-2 and EB-3 Green Card sponsorship, which is relevant for Project Managers who secure permanent roles within the organization.
What qualifications does Amgen expect for Project Manager roles?
Most Project Manager postings at Amgen expect a bachelor's degree in a life sciences, engineering, or business field, with several years of project coordination experience in a regulated biotech or pharmaceutical environment. PMP certification is commonly listed as preferred or required. Roles tied to clinical or regulatory programs often expect familiarity with IND submissions, clinical trial operations, or FDA regulatory milestones rather than general project management backgrounds.
How long does the visa sponsorship process take if I receive an offer from Amgen?
Timeline depends on visa category. E-3 and TN sponsorship can move quickly since both are processed at a consulate or port of entry without USCIS adjudication. H-1B sponsorship follows the annual lottery with an October 1 start date, though Amgen can file with premium processing to get a USCIS decision within a few business days once selected. PERM-based Green Card sponsorship typically runs one to three years depending on your priority date and country of chargeability.