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PF

QC Lab Analyst III

Pfizer
Rocky Mount, United Statesfull_timeVerifiedPosted 19 May 2025
💰 $84,580/yr

About the role

Use Your Power for Purpose

Every day, Pfizer’s unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our science and risk-based compliant quality culture is both flexible and innovative, always putting the patient first. Whether you are involved in development, maintenance, compliance, or research analysis, your contribution directly impacts patients.

What You Will Achieve

In this role, you will:

Perform basic analysis for raw materials, in process, finished products, and/or adhoc/validation/investigational testing in a safe, compliant, and efficient manner. The Job responsibilities include performing wet chemistry and analytical testing to evaluate the quality of the incoming raw materials and analyze the finished product to demonstrate that the quality of our products meet the high standards of quality.

Report testing results through computerized systems, or through standard laboratory paper-based documentation. Other related duties essential to these operations or special assignments as required.

Provides technical support as necessary to the assigned laboratory. Investigates, analyzes, problem solves, and communicates technical information to internal and external customers. Other related duties essential to these operations or special assignments as required.

Train and supports inexperienced analysts, working as a Certified Fellow Employee and mentor to aid in their development as analysts.

Other Requirements

  • Consistently adheres to company, site, and laboratory safety rules and immediately raises any safety issues with supervision as soon as they are identified.

  • Follows procedures at all times, adopting cGMP, cGDP practices.

  • Follows supervisor directions at all times.

  • Able to function independently, but asks questions as necessary

  • Accepts dynamic work sequences

  • Must be self-motivated and work with minimal direction

  • Must have strong technical and/or leadership skills

  • Routinely participates in daily Shift Handover, including discussions on improving planning communication, and teamwork efforts in the QC laboratory (where applicable for function).

  • Actively participates in daily and weekly planning discussions with his/her teammates and supervision (as needed) offering suggestions to improve Right First Time and schedule adherence as needed

  • Works with supervision and management to identify opportunities to improve testing efficiencies and actively participates in subsequent related projects

  • Consistently communicates work sequence status to supervisor in a timely manner.

  • Where scheduled work was not achieved, actively participates in discussions to identify opportunities for correction and improvement and actively works on efforts to recover adherence gaps

  • Demonstrates engagement in helping to achieve QC laboratory, team, and individual goals.

  • Whenfaced with roadblocks and issues, routinely offers suggestions for improvements and actively participates in associated improvement activities wherever possible

  • Is a positive influence on the QC laboratory, often going out of his/her way to support and assist teammates on the same shift and across shifts wherever possible.

  • Mainta

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Company

Pfizer

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