Use Your Power for Purpose
At Pfizer, every action is grounded in a steadfast commitment to delivering safe and effective products to patients. The organization fosters a science- and risk-based quality culture that is flexible, innovative, and customer oriented. Whether your role involves development, maintenance, compliance, or research analysis, your contributions have a direct impact on patient outcomes.
Position Overview
The Quality Compliance Lead serves as a strategic leader and the primary compliance lead within the Andover Pharmaceutical Sciences Quality Assurance (PSOQ) team. This role is pivotal in driving site-wide Pharmsci (PS) compliance initiatives, developing risk management strategies, and providing quality inspection readiness oversight for GMP operations. The Quality Compliance Lead ensures applicable facilities adherence to both global regulatory requirements and internal Pfizer quality procedures. Responsibilities include leading complex compliance programs, managing audits, and overseeing cross-functional projects that reinforce regulatory preparedness and mitigate risks.
Supports the PS global internal audit program and RQA internal audit team, driving compliance initiatives and audit programs across multiple Pfizer PS sites.
Key Responsibilities
Compliance Leadership & Governance
Serve as the primary compliance lead for BTx PSOQ, offering strategic guidance on global regulations, industry standards, and internal quality policies.
Lead the development and implementation of proactive compliance strategies to cultivate a culture of quality and continuous improvement.
Act as PSOQ compliance lead for regulatory inspections and audits.
Collaborate with Pfizer corporate auditors on conducting internal audits.
Lead cross-functional compliance projects across multiple sites with the global PS team to ensure regulatory readiness and reduce risks.
Collaborate with auditors and stakeholders to influence broader processes and standards.
Risk Assessment & Quality Systems
Deliver compliance support thorough risk assessments.
Advise stakeholders on risk prioritization and remediation strategies to ensure consistency with required quality expectations.
Develop and implement risk management strategies for complex, multi-site operations and major capital projects.
Quality Oversight
Work with cross-functional teams to implement quality activities and ensure compliance.
Review SOPs and documents for regulatory or internal requirements.
Create and maintain quality tools and conduct compliance training.
Manage quality assessments, risk management, CAPA plans, and/or other compliance documentation.
Track quality metrics to support audit and inspection readiness to ensure compliance.
Oversee compliance aspects for major capital projects, ensuring regulatory and internal standards are met throughout all phases of project lifecycles.
Leadership Impact
Lead compliance projects, acting as a strategic leader, that impact multiple sites and contribute to the global PSOQ compliance strategy.
Partner with key stakeholders for quality reviews, audits, investigations, and process improvement initiatives.
Drive innovative solutions to enhance efficiency and compliance across GMP operations.
Acts as a strategic leader, influencing across functions and leading complex projects without direct authority.
Minimum Requirements
BA/BS with at least 6 years of experience; OR a master's degree with at least 5 years of experience; OR a PhD with 1+ years of experience in GMP compliance and/or operations quality oversight.
Demonstrated expertise in regulatory requirements, risk management, and audit leadership.
Ability to influence across functions and lead complex projects without direct authority.
Excellent communication and negotiation skills, with experience interfacing with regulatory agencies.
Extensive experience in enterprise-wide compliance leadership and audit management.
Exceptional presentation & facilitation skills with an ability to succinctly & creatively present messages.
Willingness to contribute fresh & innovative ideas
Fluent in English
Bonus points if you have (Preferred requirements)
Experience in coaching, developing and influencing people at various levels of the organization.
Independent, quick learner with a curious & lifelong learner mindset.
Candidate demonstrates a breath 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 impact.
Strong project management skills with the ability to manage multiple priorities.
Ability to adapt to changing regulatory environment and business needs.
PHYSICAL/MENTAL REQUIREMENTS
Ability to work collaboratively on teams within a general office environment, utilizing computers.
NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS
Business travel is required to other Pfizer sites, alliance partners, and external suppliers.
This position does not include direct reports, but requires significant leadership influence.
Role is based at Pfizer Andover, MA.
Other Job Details:
Last day to Apply: January 16th, 2026
Work Location Assignment: Hybrid
Relocation assistance may be available based on business needs and/or eligibility.
Sunshine Act
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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.
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