QC Coordinator

We’re in relentless pursuit of breakthroughs that change patients’ lives. We innovate every day to make the world a healthier place.

To fully realize Pfizer’s purpose – Breakthroughs that change patients’ lives – we have established a clear set of expectations regarding “what” we need to achieve for patients and “how” we will go about achieving those goals.

Pfizer Global Supply proudly shoulders the responsibility of manufacturing and distributing our wide-ranging pharmaceutical products.

Pfizer offers competitive compensation and benefits programs designed to meet the diverse needs of our colleagues.

This position supports commercial manufacturing and the QC testing labs by managing the delivery and storage of samples. Sample types may include release test, backups, retains, reference material, assay controls, and stability. The role also supports and maintains the retain program as required by regulatory agencies and Boards of Health and monitors environmental chambers critical to the storage of these sample types.

• Coordinate receipt and delivery of samples from designated sample ports to QC laboratories or QC cGMP areas and maintain the inventory for retain samples, backup samples, and reference material.
• Adhere to Good Manufacturing Practices (cGMP) and proper documentation practices by generating, reviewing, and reconciling department records.
• Utilize sampling plans effectively and report any problems or adverse quality events to management and Quality Assurance.
• Maintain sample inventories and monitor and maintain QC Cold storage units; perform space evaluations for receipt of material.
• Assist in sampling for laboratory control testing, stability testing, and other special purposes.
• Perform data entry and distribution of inventory reports.
• Participate in on‑call program – be part of the rotation to support critical equipment 24/7.
• Coordinate and maintain Standard Operating Procedures (SOPs) within the Document Management System (DMS).
• Represent the functional group at meetings related to projects, investigations, or issues.
• Attend meetings for investigations, as required.
• Undertake other duties related to Quality Control or special projects as assigned, manage personal time and growth, and participate in process improvement teams.

• May cross‑train and provide support for other areas, such as QC Biological Shipping and Receiving, QC Sampling Operations, Solutions Chemistry, and QC Stability Operations.

• High School Diploma or GED.
• Ability to multi‑task across various capabilities and functions while managing competing priorities and requirements.
• Effective interpersonal and communication skills.
• Working knowledge of Microsoft Office applications.
• Ability to work effectively in a collaborative team environment.

• Familiarity with Quality Tracking Systems.
• 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.
• Biotechnology Certificate.
• Labware LIMS Experience.
• Experience working in a GMP facility.
• IATA and 49 CFR certification.

• 1st shift, Sunday through Thursday (weekend differential applies).
• Some holiday coverage required.

Ability to lift up to 50lbs (assisted).

50‑75% of time standing and/or walking.

Last Date to Apply for Job:
Feb 18, 2026.

Referral Bonus Eligibility: YES.

Eligible for Relocation Package: NO.

Work Location Assignment:
On Premise.

The salary for this position ranges from $24.22 to $40.36 per hour. In addition, this position offers eligibility for overtime, weekend, holiday and other pay premiums depending on the work schedule and the Company’s policies. Pfizer offers comprehensive and generous benefits and programs to help our colleagues lead healthy lives. Benefits include a 401(k) plan with matching…