Manager - CI & Investigation

Use Your Power for Purpose
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.
What You Will Achieve
In this role, you will:

• Lead and manage people, technology, and financial resources within the department, ensuring alignment with short-term goals.
• Actively share knowledge and identify potential improvements in processes or products, taking risks to develop innovative ideas.
• Solve moderately complex problems within the department and assist with issues outside the department when needed.
• Oversee operational activities and manage multiple projects, often involving cross-functional representatives.
• Recognize development needs in others, collaborate on development plans, and manage direct reports through goal setting, coaching, and ongoing assessment.
• Communicate effectively by soliciting input, explaining complex concepts, and persuading others to adopt a point of view.
• Support the Compliance Lead with resource planning, measuring team productivity, and identifying issues or opportunities.
• Ensure inspection readiness by maintaining processes, providing guidance to QC Laboratories, and communicating key learnings from regulatory audits.
• Stay updated on regulatory trends and Pfizer Quality Standards, recommending modifications to procedures and specifications as necessary.
• Collaborate with Pfizer Global Supply groups, maintain vendor service contracts, manage Quality Control Technical Services, and assist in preparing the annual budget.

Here Is What You Need (Minimum Requirements)

• M. Pharm with at least 10+ years of experience or MBA/MS with at least 8+ years of experience or PhD/JD with any years of experience or associate's degree with at least 12+ years of experience
• Experience in auditing with Good Manufacturing Practices (cGMP) regulated industries
• A successful track record of continuous improvement and the development/implementation of best practices in Quality Operations or manufacturing
• Knowledge of national and international regulations relevant to the production and control of pharmaceutical products
• Highly motivated, organized, and able to work effectively in a demanding environment with flexibility to changing priorities
• Fluency in English, both speaking and writing

Bonus Points If You Have (Preferred Requirements)

• Master's degree with relevant pharmaceutical experience, particularly in aseptic manufacturing
• Experience with electronic systems including Laboratory Information Management System Application and Products, MS Word, and MS Excel
• Demonstrated leadership capabilities
• Ability to adapt to a fast-paced and changing environment
• Experience using common AI tools, including generative technologies such as ChatGPT or Microsoft Copilot, to support problem solving and enhance

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
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 .
Quality Assurance and Control