Full-Time

Senior Director Product Management

Posted on 9/9/2026

Deadline 9/17/26
Pfizer

Pfizer

10,001+ employees

Biopharmaceutical company develops medicines and vaccines

Compensation Overview

$214.9k - $358.1k/yr

+ 22.5% bonus target + Share-based long-term incentive program

No H1B Sponsorship

Collegeville, PA, USA + 1 more

More locations: New York, NY, USA

Hybrid

Hybrid schedule requires working on site 2 to 3 days per week.

Bachelor's, Master's, MBA

Category
Product (1)
Required Skills
Agile
Product Management
Machine Learning
SCRUM
Data Governance

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Requirements
  • 12+ years of progressive experience in product management or product ownership, including at least 4–5 years operating at a senior or director level owning products end-to-end.
  • Experience translating enterprise or life-sciences business strategy into product roadmaps and requirements at scale.
  • Experience translating business needs into artificial-intelligence-based technical solutions that have successfully scaled globally.
  • A proven track record managing senior VP- and SVP-level stakeholder relationships and driving prioritization decisions across competing interests.
  • Experience with agile or iterative delivery frameworks such as Scaled Agile Framework, Scrum, or equivalent, and modern product management practices including discovery, experimentation, minimum viable products, and outcome-based roadmapping.
  • A bachelor's degree.
  • Ability to influence and collaborate with peers, develop and coach others, and oversee and guide colleagues' work to achieve meaningful outcomes and business impact.
  • Ability to travel to Pfizer offices, vendor offices, and other team meeting locations when required.
  • Ability to work during off-hours when necessary to coordinate with global stakeholders.
  • Authorization to be employed in the United States by any employer, with permanent work authorization required.
Responsibilities
  • Own the end-to-end product vision, strategy, and roadmap for one or more global Medical Affairs artificial intelligence and digital products, from initial ideation through scaled global deployment.
  • Serve as the implementation lead for developing global products, engage broad stakeholders across Medical Affairs, and report progress to Air Traffic Control.
  • Translate enterprise and Medical Affairs strategic priorities into a product strategy with clear value hypotheses, target outcomes, and success metrics.
  • Continuously evaluate therapeutic-area, market, and regulatory trends, including health technology assessment and the European Union Artificial Intelligence Act, to keep the roadmap ahead of business needs.
  • Collaborate with Commercial product leads to define integration points to Commercially led products.
  • Serve as the primary product point of contact for a broad, senior stakeholder base across global Medical Affairs, Oncology, International, and adjacent functions.
  • Elicit, synthesize, and translate ambiguous or conflicting business needs from multiple senior stakeholders into clear, documented product, feature, and technical requirements.
  • Facilitate structured prioritization and trade-off discussions among VP- and SVP-level stakeholders, build consensus where interests diverge, and make the final call when consensus is not reached.
  • Define and document detailed product, feature, and technical requirements, acceptance criteria, and success measures in partnership with user experience, architecture, and engineering.
  • Own and continuously groom the product backlog and roadmap, sequencing features by business value, dependency, and delivery feasibility.
  • Partner with Solution Architecture and Engineering to ensure feature designs are technically sound, scalable, and compliant with Pfizer's technology standards.
  • Lead products through discovery, experimentation, pilot, minimum viable product, enterprise scale, and sustained operation, applying appropriate governance rigor at each stage.
  • Define and track adoption, business value, and return-on-investment metrics post-launch, and use them to inform roadmap iteration and investment decisions.
  • Manage risk, compliance, and change-control considerations specific to Medical Affairs, including data privacy, medical, legal, and regulatory review, the European Union Artificial Intelligence Act, and health technology assessment implications.
  • Direct the work of Product Managers, Engineers, User Experience Designers, and Program Delivery Leads supporting the product without requiring formal reporting authority.
  • Represent the product in portfolio governance forums, providing status, risk, and prioritization recommendations to senior leadership.
  • Mentor and develop product talent within the broader Medical AI Acceleration and Delivery team.
Desired Qualifications
  • Pharmaceutical, life sciences, or other regulated-industry experience.
  • Medical Affairs domain knowledge.
  • Experience with artificial-intelligence and machine-learning-enabled products.
  • Understanding of responsible artificial intelligence, data governance, and emerging artificial-intelligence regulation, including the European Union Artificial Intelligence Act.
  • An MBA or advanced degree.

Pfizer is a global biopharmaceutical company that discovers, develops, manufactures, and sells medicines and vaccines for a range of health needs, including vaccines, oncology, and other specialized therapies. Its products work by using biological mechanisms to prevent or treat diseases—vaccines train the immune system to fight infections, while medicines target cancer and other conditions. Pfizer differentiates itself through its large worldwide footprint, broad portfolio across multiple therapeutic areas, and partnerships (notably with BioNTech) that expanded its reach in vaccines and cutting-edge therapies. The company also engages in public health initiatives, such as efforts to provide vaccines to underserved populations. Pfizer’s broad goal is to improve global health by delivering safe and effective medicines and vaccines through research, development, and wide international distribution.

Company Size

10,001+

Company Stage

IPO

Headquarters

New York City, New York

Founded

1849

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Simplify Jobs

Simplify's Take

What believers are saying

  • FDA approved Pfizer-BioNTech’s XFG COVID vaccine on August 27, 2026 for fall shipping.
  • Pfizer raised 2026 revenue guidance to $60.5 billion-$62.5 billion on August 4, 2026.
  • Padcev and Lorbrena grew in Q2 2026, proving post-Seagen oncology momentum.

What critics are saying

  • Eliquis loses U.S. exclusivity in 2028, opening a rapid generic cliff.
  • Arbutus filed international LNP patent suits on July 16, 2026 against Pfizer-BioNTech.
  • Comirnaty and Paxlovid remain shrinking as FDA narrows eligibility and COVID demand fades.

What makes Pfizer unique

  • Pfizer’s Seagen acquisition gives it a stronger oncology engine than pure-vaccine peers.
  • Eliquis and Vyndaqel diversify revenue beyond COVID, with Q2 2026 growth.
  • Pfizer’s global commercial scale still pushes products through pharmacies, hospitals, and governments.

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Benefits

Health Insurance

Dental Insurance

Vision Insurance

401(k) Retirement Plan

401(k) Company Match

Paid Vacation

Paid Sick Leave

Paid Holidays

Hybrid Work Options

Relocation Assistance

Growth & Insights and Company News

Headcount

6 month growth

-5%

1 year growth

-5%

2 year growth

-5%
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Sep 8th, 2026
AbbVie beats Pfizer as top dividend stock with 53-year payout streak and 203% growth

AbbVie offers a smarter long-term dividend investment than Pfizer, despite Pfizer's higher 6.1% yield. AbbVie holds Dividend King status with 53 consecutive years of dividend increases and raised its payout by 5.5% this year to $1.73 per share. Over the past decade, AbbVie increased its dividend by more than 203% compared to Pfizer's 51%. AbbVie's revenue grew 138% during this period, whilst Pfizer's rose just 18%. AbbVie successfully navigated Humira's patent cliff through home-grown immunology drugs Skyrizi and Rinvoq. By 2025, these two drugs generated combined annual sales exceeding $25 billion, replacing Humira's peak revenue and pushing total company revenue to record highs. AbbVie's free-cash-flow dividend payout ratio stands at 65%, lower than Pfizer's 89%.

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Pfizer's updated COVID vaccine ships as FDA approves narrower rollout for over-65s and high-risk groups

Pfizer received FDA approval for its updated Comirnaty COVID-19 vaccine on Thursday, with deliveries to pharmacies and clinics beginning immediately. The company's shares were trading at $27.9079 on 28 August. However, the market opportunity has significantly narrowed from pandemic levels. Eligibility is now limited to adults aged 65 and older, plus higher-risk patients aged 5 through 64. Despite Comirnaty having distributed over five billion doses worldwide historically, today's revenue potential is considerably more constrained. Pfizer faces competition from Moderna and the Novavax-Sanofi protein vaccine for this smaller patient pool. The company's current share price sits 5.27% above its estimated value of $26.51, suggesting investors are paying a premium before actual uptake and commercial results become clear.

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Aug 27th, 2026
FDA approves Pfizer-BioNTech XFG-adapted COVID-19 vaccine for high-risk groups

Pfizer and BioNTech have received US Food and Drug Administration (FDA) approval for their 2026-2027 COVID-19 vaccine targeting the XFG variant. The vaccine is approved for adults aged 65 and older, and individuals aged 5 to 64 with underlying conditions that increase risk of severe COVID-19 outcomes. The FDA approval is based on clinical, non-clinical and real-world data demonstrating the vaccine generates strong immune responses against currently circulating SARS-CoV-2 variants, including XFG and other contemporary lineages. The XFG variant was selected following FDA guidance for fall 2026 vaccine composition. The vaccine will begin shipping immediately and will be available in US pharmacies, hospitals and clinics within days. To date, more than five billion doses of COMIRNATY have been distributed globally.

Yahoo Finance
Aug 24th, 2026
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Pfizer and Johnson & Johnson are navigating patent cliffs as key drugs lose exclusivity, with their latest results showing differing stages of transition. Pfizer's revenue excluding COVID products grew 5% operationally in Q2 2026, with newer medicines like Padcev and Vyndaqel contributing. The company expects $9.7 billion in cost savings through 2029 to support margins during the transition. Johnson & Johnson's Innovative Medicine sales rose 7.8%, despite Stelara revenue declining 55%. Tremfya sales surged 72.5% to $2 billion, helping offset losses alongside growth from oncology and neuroscience products. Johnson & Johnson raised 2026 guidance, with reported sales expected to reach $101.1 billion and adjusted EPS of $11.68. Its MedTech division provides additional diversification that pure pharmaceutical company Pfizer lacks, suggesting Johnson & Johnson's transition is more advanced.

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Intel CEO invests $10M in shares as chipmaker posts 25% revenue growth driven by AI demand

Intel CEO Lip-Bu Tan purchased nearly $10 million worth of shares as part of the chipmaker's recent stock offering, signalling confidence in the company's turnaround. Intel recently reported revenues of $16.1 billion, growing 25% year-over-year, with its Data Centre and AI business unit seeing revenue surge nearly 60% to $6.3 billion. CoStar Group founder and CEO Andrew Florance purchased 83,300 shares totalling roughly $2.5 million. Pfizer CEO Albert Bourla similarly invested, purchasing 38,000 shares for just over $1 million. These insider purchases reflect executives' confidence in their companies' longer-term outlook, with investors often viewing such moves as a positive signal.