A

Amgen

Makes biotech medicines for serious illnesses

Global Patient Safety Business Excellence Senior Manager

Full-TimeUpdated on 10/21/2026
$140.8k - $190.5k+ Annual bonus + Stock-based long-term incentives
Expert
Bachelor's, Master's, PhD, Associate's
Remote in USA
Remote
Biology & BiotechRegulatory & Quality (Life Sciences)
H1B Sponsorship Available

About the job

Requirements
  • A doctorate degree and 2 years of Safety Project Management experience, or a master’s degree and 4 years of Safety Project Management experience, or a bachelor’s degree and 6 years of Safety Project Management experience, or an associate’s degree and 10 years of Safety Project Management experience, or a high school diploma or GED and 12 years of Safety Project Management experience.
Responsibilities
  • Lead the development, implementation, and continuous improvement of project management and change management standards, methodologies, and best practices across Global Patient Safety.
  • Drive and sustain Global Patient Safety governance frameworks, ensuring effective oversight, decision-making, and alignment with organizational objectives.
  • Lead and deliver business-critical initiatives within Global Patient Safety and represent Global Patient Safety on enterprise-wide cross-functional programs.
  • Provide strategic leadership and oversight for pharmacovigilance activities related to mergers, acquisitions, licensing agreements, and divestitures.
  • Contribute to the advancement and effectiveness of the Global Patient Safety Quality Management System, ensuring compliance with global regulatory requirements.
  • Undertake activities delegated by the Qualified Person Responsible for Pharmacovigilance as detailed in the Pharmacovigilance System Master File and maintain a state of inspection readiness.
  • Support Health Authority inspections, business partner audits, and internal process audits within the remit of the role and responsibility, including logistics and operational support.
  • Develop, monitor, and report key performance and compliance metrics to support management review, strategic decision-making, and continuous improvement.
  • Facilitate cross-functional management of deviations, corrective and preventive actions, and quality improvement initiatives to ensure sustainable compliance outcomes.
  • Build and maintain strong partnerships with internal and external stakeholders, influencing decisions and driving alignment across complex organizational initiatives.
  • Champion digital transformation opportunities, including the adoption of automation, analytics, and emerging technologies to enhance Global Patient Safety.
Desired Qualifications
  • Demonstrated expertise in project management, change management, and organizational transformation.
  • Strong leadership acumen and the ability to influence without authority.
  • Ability to comprehend pharmacovigilance regulations and compliance practices, and interpret multiple requirements into concise, clear instructions.
  • Ability to work in an international environment and with cross-functional teams, with interpersonal skills, assertiveness, team spirit, and coaching skills.
  • Critical thinking and decision-making skills; comfort with ambiguity and ability to work independently as needed.
  • Ability to manage time and priority constraints and multiple priorities simultaneously.
  • Demonstrated ability to leverage digital technologies, automation, and data-driven insights to improve operational effectiveness and business outcomes.
  • Strength in facilitation, both virtual and in person, including with executive leadership.
  • Project Management Professional certification or equivalent in Change or Project Management.
  • A history of successful execution of major projects in a regulatory or safety environment.
  • Experience with mergers, acquisitions, and divestitures in Life Sciences.
  • Strong leadership experience, ideally with fully remote teams across time zones.
  • Significant experience within pharmacovigilance, drug safety, regulatory affairs, quality, or related life sciences functions.
  • Proven experience establishing governance frameworks and leading complex, enterprise-wide initiatives.
  • Experience presenting to and influencing senior leadership and executive stakeholders.
  • Strong analytical skills and ability to translate data into actionable business recommendations.
  • Experience leading process improvement initiatives using Lean, Six Sigma, Agile, or similar methodologies.

About the company

Amgen develops and makes biologic medicines, which are drugs built from proteins and antibodies grown in living cells, for serious conditions such as heart disease, cancer, and bone loss. Its anemia drug Epogen, approved in 1989, became one of the biotechnology industry's first blockbuster medicines. Amgen grows these drugs in large tanks called bioreactors, and its products include the cholesterol drug Repatha, the bone-building drug Evenity, and the severe asthma drug Tezspire. It earns money by selling these medicines, mostly through large drug wholesalers that supply hospitals and pharmacies. Amgen was founded in 1980 and is based in Thousand Oaks, California.

Company Size

10,001+

Company Stage

IPO

Headquarters

Thousand Oaks, California

Founded

1980

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Simplify's Take

What believers are saying

  • Growth is broad-based: 22 products grew at least 10%, lifting June 2026 quarter revenue 10% to $10.1 billion.
  • Stock grants gained value: Amgen shares rose 27% from January to October 9, 2026, versus 10% for rival Eli Lilly.
  • Many U.S. roles are remote: 145 of Amgen's 615 U.S. job openings in October 2026 were fully remote.

What critics are saying

  • Its 2025 best seller is shrinking: cheaper copies cut bone drug Prolia's sales 32% in the June 2026 quarter.
  • MariTide, Amgen's obesity bet, faces a giant: Lilly's Mounjaro and Zepbound outsold all of Amgen in the June 2026 quarter.
  • Most tech openings are in India: 156 of Amgen's 210 information systems jobs in October 2026 were in Hyderabad.

What makes Amgen unique

  • It copies rivals' blockbusters too: Pavblu, its version of Regeneron's eye drug Eylea, sold $700 million in 2025.
  • Amgen hunts drug targets in a nation's DNA: its Icelandic unit deCODE has genetic data on two-thirds of Iceland's adults.
  • Amgen opened a U.S. cancer-drug class: Blincyto, approved in 2014, was the first to tether immune cells to cancer.

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Benefits

  • Professional Development Budget
  • Conference Attendance Budget

Company News

Yahoo Finance
Oct 20th, 2026
Johnson & Johnson and Amgen beat the market in 2026, but can the dividend stocks keep going?

Johnson & Johnson and Amgen, two dividend stocks that have beaten the broader market this year, could suit investors bracing for a possible crash. J&J's latest quarter beat expectations, and it slightly raised its 2026 guidance. But its medtech unit is struggling, as demand for the Impella heart pump has fallen amid safety questions and a US Class 1 recall. Long-term, it has new drugs, a robotic surgery system approved in the US, and a proposed $5.5 billion talc settlement. It is a Dividend King with 64 straight years of payout increases. Amgen's second-quarter revenue rose 10% to $10.1 billion, despite pressure on Tavneos and falling denosumab sales. It has raised payouts 152% over a decade and offers a 2.3% forward yield, against 1.1% for the S&P 500.

Yahoo Finance
Oct 17th, 2026
Amgen raises 2026 revenue forecast to $38.8B as shares gain 15.2%

Amgen raised its fiscal 2026 revenue forecast on August 4 to $38.8 billion at the midpoint, up 2.6% from $37.8 billion. Adjusted earnings per share guidance rose to $22.90 from $22.40. Six key growth drugs grew 26% from a year earlier and made up nearly 70% of product sales in the June quarter. Repatha sales rose 37% to $953 million, offsetting a 33% drop in Prolia and XGEVA sales as biosimilar copies launched. Total revenue rose 10%. The stock has gained 15.2% since the release, against 1.9% for the S&P 500. It closed at $434.03 on October 15, above both its 50-day and 200-day averages. Reaching the midpoint requires $20.1 billion in the second half. Amgen's next report is expected around November 3.

Yahoo Finance
Oct 8th, 2026
Amgen invests $2.6B in manufacturing for MariTide obesity drug ahead of Phase III results

Amgen is testing MariTide, an experimental obesity drug designed to be dosed monthly or less frequently. The therapy has advanced into late-stage Phase III trials, with nine studies currently running and three more planned. Executives reported strong enrolment during the company's second-quarter 2026 earnings call on 4 August 2026. Amgen expects capital spending of about $2.6 billion in 2026, partly to scale manufacturing capacity for MariTide's eventual launch. The company is investing across its US manufacturing sites in North Carolina, Ohio, and Puerto Rico. Amgen stock has returned 44% over the past twelve months, outpacing the S&P 500's 17.1% gain. The company reported $38.1 billion in revenue over the last twelve months, up from $34.9 billion a year earlier.

Yahoo Finance
Sep 29th, 2026
Amgen lifts dividend 6%, but eroding Prolia and Enbrel sales shift focus to MariTide Phase 3

Amgen raised its quarterly dividend 6% to $2.52 per share, marking its 14th consecutive annual increase since starting payouts in 2011. The biotech now pays $10.08 annually, yielding 2.36% at current share prices of $418.13. The dividend appears well covered. Amgen generated $8.1 billion in free cash flow in 2025 against $5.1 billion in dividend payments. Second quarter 2026 free cash flow reached $3.5 billion whilst dividends consumed $1.4 billion. However, biosimilar competition is eroding legacy revenue. Prolia and XGEVA sales dropped 33% whilst Enbrel fell 37%. The company carries $57 billion in debt. Future dividend growth may hinge on Phase 3 results for MariTide, Amgen's obesity candidate. The company follows a steady raise pattern similar to Johnson & Johnson, contrasting with Pfizer's post-COVID payout struggles.

Yahoo Finance
Sep 26th, 2026
Vertex and Amgen deliver promising pipeline updates as both outperform market

Vertex Pharmaceuticals reported strong second-quarter results, with revenue rising 12% year-over-year to $3.33 billion and earnings per share climbing 8% to $4.31. The company posted positive Phase 2b results for inaxaplin, an experimental treatment for APOL1-mediated kidney disease, showing it reduced proteinuria in patients with modest protein levels and those with type 2 diabetes. Vertex expects approval for povetacicept, a treatment for IgA nephropathy, by November. The company continues diversifying beyond its core cystic fibrosis franchise, which provides predictable revenue as patients require lifelong treatment. Meanwhile, Amgen has also outperformed the broader market this year, though specific recent developments were not detailed in the source material.