Pfizer Limited Posted October 30, 2026

Director, QSEO AI Transformation Lead

Collegeville, United States Full time
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Pfizer Limited is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

ROLE SUMMARY

The Director, QSEO AI Transformation Lead provides strategic and subject-matter leadership for artificial intelligence governance, quality oversight and responsible adoption across Pfizer Global Supply (PGS) and Quality, Safety, Environment & Operations (QSEO). The role enables the Native-AI vision by establishing the governance, quality frameworks and AI life-cycle practices needed to accelerate AI adoption while maintaining appropriate GxP controls, regulatory compliance and inspection readiness.

Operating at the intersection of Quality, Digital and Operations, the Director applies deep functional expertise and independent judgment to complex and evolving AI opportunities, risks and regulatory expectations. The role translates these considerations into practical, risk-based approaches that enable innovation and process simplification while maintaining appropriate oversight throughout the AI life cycle.

Working across organizational and functional boundaries, the Director leads complex cross-functional initiatives, leads a team and influences alignment and advises senior leaders on AI governance, risk, compliance and deployment considerations. The role anticipates emerging issues, develops recommendations and drives resolution of complex challenges through matrix leadership and subject-matter expertise.

ROLE RESPONSIBILITIES

Provide strategic leadership for QSEO AI transformation, governance and quality oversight across the PGS AI portfolio.

Translate the Native-AI vision into governance strategies, quality approaches and implementation plans that accelerate responsible AI adoption.

Advise senior leaders on AI opportunities, regulatory expectations, GxP risks, investment priorities and deployment considerations.

Establish and maintain risk-based quality oversight for Digital and federated AI solutions throughout the AI life cycle.

Lead the AI Quality Review Board and GxP AI Steering Committee, driving effective decisions, escalation and closure of agreed actions.

Establish portfolio-level approaches for AI audit and inspection readiness, identifying systemic risks and recommending corrective or preventive actions.

Monitor emerging AI regulations, standards and industry practices and translate their implications into practical internal requirements and recommendations.

Represent QSEO in enterprise AI governance forums and lead resolution of actions arising from the PGS AI Council.

Provide strategic leadership for maintenance, adoption and continuous improvement of the AI life-cycle process.

Simplify AI governance and delivery processes while maintaining appropriate quality, compliance and risk controls.

Establish expectations for accurate AI inventory management and influence an integrated enterprise approach to AI life-cycle visibility.

Define and advance a portfolio-level approach for monitoring the health, performance and control status of GxP-relevant AI solutions.

Provide strategic direction for PGS AI governance and quality tools, including AIRIF and AIQAS, and their alignment with the PGS platform strategy.

Establish and guide the QSEO AI community of practice, partnering with PGS GxP AI ambassadors and relevant PGS, Digital and Research & Development organizations.

Develop portfolio metrics and insights that provide senior leaders with visibility into AI adoption, quality, compliance, risk and value.

Lead QSEO AI-related IMEx reporting, resource visibility, risk assessment and escalation.

BASIC QUALIFICATIONS

Bachelor’s degree in a scientific, engineering, technology, data, quality or related discipline with at least eight years of relevant experience; or a master’s degree with at least seven years of relevant experience; or a doctoral degree with at least five years of relevant experience.

Significant experience in pharmaceutical quality, manufacturing, regulatory compliance, Digital quality or another regulated environment.

Demonstrated expertise in GxP quality systems, risk management, computerized systems, Digital governance, AI governance or related disciplines.

Experience applying quality and risk-management principles across the life cycle of Digital, computerized or AI-enabled solutions.

Demonstrated experience leading complex, cross-functional initiatives in a global, highly matrixed organization.

Experience supporting regulatory inspections, internal audits or inspection-readiness activities as a subject-matter expert.

Demonstrated ability to exercise independent judgment and develop recommendations for highly complex and ambiguous issues.

Proven ability to influence senior leaders and drive alignment across Quality, Digital, Operations and business stakeholders without direct authority.

Strong written and verbal communication skills, including the ability to translate technical and regulatory issues into clear business and risk insights.

Working knowledge of AI and machine-learning concepts, including model life cycle, data quality, performance monitoring, drift, explainability and human oversight.

 

PREFERRED QUALIFICATIONS

Advanced degree in a scientific, engineering, data, technology, regulatory or quality discipline.

Experience developing or implementing governance for AI or machine-learning solutions in a GxP environment.

Familiarity with applicable AI, quality and risk-management regulations, standards and guidance.

Experience leading senior governance or multidisciplinary decision-making forums.

Experience establishing portfolio-level monitoring, inspection-readiness or risk-reporting approaches.

Quality, auditing, risk-management, Digital, data or AI-related certification.

Experience applying IMEx, Lean, Six Sigma or comparable process-improvement methods.

Experience with portfolio management, governance tools, value reporting or AI inventory management.

Candidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact.

PHYSICAL/MENTAL REQUIREMENTS

Ability to evaluate multiple complex and concurrent inputs, exercise sound judgment and develop clear, actionable recommendations.

Ability to manage competing priorities and operate effectively in a complex, matrixed and globally distributed environment.

NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS

Periodic participation in meetings outside standard working hours may be required to support global stakeholders.

Occasional business travel may be required based on portfolio and program needs.

Work Location Assignment: Hybrid

Relocation Support: NO

Last date to apply: 11/12/2026

The annual base salary for this position ranges from $176,600.00 to $294,300.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 20.0% of the base salary and eligibility to participate in our share based long term incentive program. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments. Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site – U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.


This role is posted in multiple locations. If you are applying for the role in an secondary job posting location where pay transparency regulations apply, your Talent Advisor will share the local pay information with you during the first interview.



Relocation assistance may be available based on business needs and/or eligibility.

Candidates must be authorized to be employed in the U.S. by any employer.

U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.

Sunshine Act

Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations.  These laws and regulations require Pfizer to provide government agencies with information such as a health care provider’s name, address and the type of payments or other value received, generally for public disclosure.  Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act.  Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government.  If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.

EEO & Employment Eligibility

Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status.  Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA.  Pfizer is an E-Verify employer.  This position requires permanent work authorization in the United States.

Pfizer endeavors to make   www.pfizer.com/careers   accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email   disabilityrecruitment@pfizer.com . This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.

To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on  Pfizer Careers .

Information & Business Tech

Job details

Seniority
Director
Function
Information Technology
Therapeutic area
Not listed
Location
Collegeville, United States
Employment type
Full time

How this role compares

Computed from every other active Information Technology role in our database, not just this employer's listings.

We currently track 192 comparable Director Information Technology roles across 38 biopharma companies.

192Comparable roles tracked
157Currently active
38Companies hiring similar roles
19Countries represented

Salary context

46 of 192 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject $176,600/yr – $294,300/yr
Peer group range $114,650 – $328,000 (median $218,850)

Where these roles are based

Top locations among the 192 comparable roles

India84
United States76
Spain5
Argentina4
China3
United Kingdom3

+ 13 more countries

Seniority mix

192 of 192 peers have a known seniority level

Principal120
Director58
Senior Director14

Therapeutic area mix

1 of 192 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology1

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

60%similar
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Gilead Sciences, Inc. Foster City, United States Director
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Notify me about similar jobs

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How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

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Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.