QC Manager, Stability - Pfizer : Job Details

Every day, everything we do is driven by an unwavering commitment to delivering safe and effective products to patients. Our quality culture, which is both science and risk-based, is flexible, innovative, and customer-oriented. Whether you are engaged in development, maintenance, compliance, or analysis through research programs, your contribution will have a direct impact on patients. Our dedication to quality and safety ensures that we consistently meet the highest standards, making a real difference in the lives of those we serve. Join us in our mission to improve patient outcomes through excellence in every aspect of our work.

The Quality Control Stability Manager is responsible for the management of Stability group to ensure that quality control cGMP activities in support of the clinical and commercial stability testing of products manufactured at the Sanford site are conducted within site, corporate, and regulatory requirements. The scope of the position includes all activities associated with stability studies and QA reserve samples for multiple types of products.

In this role, you will:

• Provide strategic and scientific oversight to the stability team
• Ensure Stability studies are managed and handled per site and global procedures and guidelines
• Responsible for colleagues objective setting, conducting one on one meetings with Colleagues, providing guidance/coaching, assisting with colleague development planning, and completing performance reviews
• Determine appropriate training curriculums for colleagues
• Responsible for review, approval and final authorization of cGXP documentation (e.g. data records, reports, protocols, batch records, etc.) and ensuring adherence to regulatory agency requirements, ICH guidelines, Pfizer standards, policies, and values.
• Manage a working area and manage projects/changes to accomplish change activities/project deliverables and/or whole projects; responsible for prioritization and associated timely completion of activities/deliverables and/or project timelines
• Responsible for participating in, leading, or providing guidance for investigations
• Serve on or leads cross functional teams to represent QC stability and facilitate communications and activities/projects between Quality Operations and site departments and/or Network
• Responsible for assessing existing situations and suggesting continuous improvements to increase compliance and innovation
• Plans and leads complex, high business impact projects to ensure their timely completion
• Established interpersonal skills (negotiation, managing conflict) to influence team
• Work is achieved by individual or through project teams, utilizing technical or subject matter expertise to achieve results
• Requires relevant scientific education, skills, and knowledge

Here is what you need (minimum requirements):

• Applicant must have a bachelor's degree with at least 4 years of experience; OR a master's degree with at least 2 years of experience; OR a PhD with 0+ years of experience; OR an associate's degree with 8 years of experience; OR a high school diploma (or equivalent) and 10 years of relevant experience
• Experience in QC/laboratory management
• Previous leadership experience required, and experience leading people leaders is preferred
• Strong background in Quality Control
• Extensive knowledge of Good Manufacturing Practices (cGMP) compliance requirements for Quality Control Laboratories

Physical/mental requirements:

Ability to stand for 1 hour at a time, sit for 2 to 3 hours at a time, walk long distances and bend to obtain items from lower shelving/cabinets

Non-standard work schedule, travel or environment requirements:

Work schedule may include weekdays and/or weekend days with first, second, and/or third shift hours as appropriate for assigned tasks/activities. Limited travel for the position; no more than 15% traveling.

Last Date to Apply for Job: August 20, 2025.

Referral Bonus Eligibility: YES

Eligible for Relocation Package: NO

Relocation support available

Work Location Assignment: On Premise

The annual base salary for this position ranges from $102,900 to $171,500. In addition, this position is eligible for participation in Pfizer's Global Performance Plan with a bonus target of 15% 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 lifes 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.