What You Will Achieve

The role is responsible for implementing and overseeing the processes and programs for Pharm Sci Sm. Molecule (PSSM (PTx)) GMP R&D pipeline programs. This position has key responsibilities for the execution of the PTx Portfolio, leading to seamless lifecycle management and ultimate transfer to Pfizer Global Supply (PGS) sites or Contract Manufacturing Organizations (CMOs).

This position includes instilling and influencing a strong quality culture at multiple Pharm Sci and PGS PTx-facing sites globally. This position requires solid understanding of compliance regulations, process validation, Quality by Design concepts, and quality systems as they relate to manufacturing, testing, stability, scale-up, and development of solid, semi-solid small molecule dosage forms, diagnostics, and combination products.

The successful candidate’s ability to meet project targets will help in completing critical deliverables. Innovative use of communication tools and techniques will facilitate explaining issues and create a collaborative team environment across various internal and external Quality groups, Pharm Sci and PGS.

How You Will Achieve It

•    Lead projects with complete accountability for Quality oversight of complex PSSM(PTx) projects inclusive of the following:

○   Acquired assets/companies & associated Quality Integrations/Quality Integration Plans

○   Partnerships/Collaborations with other Pharma Companies

○   Internal PTx pipeline programs. Many programs will be at an accelerated pace inclusive of programs which have a formally accelerated review with FDA or other boards of health due to an unmet medical need.

○   Provide Quality & Compliance oversight to programs assigned

This position is responsible for providing quality oversight to PTx portfolio projects including disposition of Clinical Trial Material (CTM) drug substance, API, drug product intermediate, drug product, drug product, peptides, PTx products, including various modalities and combination products.

•    Work with multiple CMOs, acquired, in licensed or out licensed companies, Pharm Sci, and PGS PTx-facing sites responsible for development, manufacturing, and testing investigational medicinal product supplies for use in human clinical trials. Establish and adhere to norms for collaboration and roles & responsibilities with other sites and quality groups.

•    Act as PSOQ quality point of contact to PSPT and CDT project teams, PTx Pharm Sci sites, and various PGS sites to programs assigned.

•    In collaboration with other groups, interpret, advise, and execute against evolving compliance regulations with respect to new focus areas or novel technologies/modalities such as multi-specifics, SDD, peptides, nanoparticles, traditional oncology, I&I and I&M therapies.

•    Provide Quality oversight to external vendors/CMOs/acquired companies/partners responsible for manufacturing of drug substance, API, drug product intermediate or drug product including, but not limited to, release of materials for use in human clinical trials.

•    In collaboration with business lines and Global Chemistry, Manufacturing and Controls (GCMC)/Global Regulatory Affairs(GRA) develop control and release strategies for projects assigned.

•    Review/approve PSOQ global procedures that may impact quality systems and quality of CTM ensuring alignment with Pfizer GSOPs and GWIs and smooth interface with PGS sites as applicable. Work to develop procedures/processes that increase efficiency and maintain high-quality standards.

•    In consultation with PSOQ PTx Portfolio lead, determines when a Notification to Management should be issued for a significant quality or compliance event. Author NTM.

•    Provide training, guidance, and coaching to QA colleagues participating in various projects.

•    Manage own time to meet agreed targets and develop plans for work activities within matrixed teams inclusive of Pharm Sci, PGS, or external CMO sites.

•    Manage and author Quality Assurance Agreements in support of PTx programs inclusive of alliance partnerships & acquisitions and other pharma collaborations.

•    Make GMP compliance and Quality decisions independently to resolve complex issues.

•    Review complex investigations and provide guidance to colleagues and project teams on investigations including Notifications to Management and Significant Quality Events (SQE). Support PSOQ PTx Portfolio Lead with Quality Review Teams (i.e., Area Quality Review Team (AQRT), PharmSci Quality Review Team (PSQRT) and product recalls.

•    Provide direction and support to PSOQ /PTx Pharm Sci sites relative to a constant state of inspection readiness. Participate in audits/inspections (inclusive of Pre-Approval Inspections) as needed.

•    Recognize when an issue is beyond your sphere of influence and escalate to PSOQ LT leader.

•    Participate in or lead Limited Duration Teams, Right First Time (RFT), and Continuous Improvement projects, Corrective/Preventative Action Effectiveness, which may be PSOQ-centric or cross-functional where impact may often be global in nature.

•    Help to define appropriate action plans for improvement and follow-up and communicate action closures across both Pharm Sci and PGS

•    Lead and support initiatives that contribute to strengthening quality culture from a global and site perspective across Pharm Sci and PGS sites. Practice and encourage quality culture behaviors within quality and the business lines.

Here Is What You Need (Minimum Requirements)

• Applicant must have a bachelor's degree, in a scientific discipline preferred, 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​
• Relevant experience in the pharmaceutical industry.
• Sound knowledge of PTx manufacturing and testing technology for various modalities.
• 4+ years' experience in PTx Portfolio project overseeing PSPT and Co-Dev teams for Quality and Compliance.
• Sound knowledge of current Good Manufacturing Practices and the applicable GxP regulations and standards.
• Sound knowledge of GMP documentation review inclusive of investigations/CAPA/change management, test methods, master and executed batch records, stability data, etc.
• Experience with GMP electronic systems and tools.
• Experience and talent in mediation and negotiation skills.
• Ability to work independently as well as in a team environment within own team and interdepartmental/matrixed teams.
• Excellent communication and interpersonal skills.
• Proactive approach and strong critical thinking skills.
• Effective written and oral communication skills.
• Self-motivated, engaged, and able to perform moderately complex tasks independently.

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.

Bonus Points If You Have (Preferred Requirements)

• Master’s degree
• Extensive pharmaceutical industry experience in operational risk, compliance management, and hands-on roles in Quality Operations (QO), Operations, and Quality Control (QC)
• A solid technical and practical understanding of various dosage forms
• Strong analytical and problem-solving skills
• Ability to influence and lead cross-functional teams
• Experience using common AI tools, including generative technologies such as ChatGPT or Microsoft Copilot, to support problem solving and enhance productivity. Demonstrated curiosity for exploring how these tools can improve outcomes and understanding of responsible AI practices, including risk management and ethical use

 
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

•    Mental agility to handle a large quantity and broad scope of different types of Quality Assurance Agreement partnerships.

•    Ability to work independently, problem-solve, and make recommendations for solutions.

•    Role is primarily office/computer based.

Able to lead and/or participate in person or virtual meetings.

NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS

•    Flex/Hybrid Monday - Friday, typically 8:00am to 4:30pm.

•    Some travel required, approximately 4x per year, to support team kickoff meetings, etc.

•    Shift Differential: NOT ELIGIBLE

Work Location Assignment: Hybrid

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.