Quality Control Raw Materials Sampling Associate

Pfizer•Andover, MA
•$60,200 - $100,400•Onsite

About The Position

The Quality Control Analytical group is seeking a highly motivated candidate to support GMP sampling and analytical testing of raw materials at the Andover site. The role supports clinical and commercial manufacturing operations through raw material sampling, testing, and related activities. The position is on premise and operates on first shift, Monday through Friday, with occasional off-hours support potentially required for staff and operations.

Requirements

  • Bachelor's degree with any years of experience, or an associate's degree with 4 years of relevant experience, or a high school diploma (or equivalent) and 6 years of relevant experience.
  • Experience performing QC analytical testing and following procedures in a GMP laboratory.
  • Strong understanding of cGMP regulations.
  • Proficiency with computer systems, including Microsoft Office applications and LIMS.
  • Ability to lift 50–100 pounds daily and walk, lift, and move materials in a warehouse for 5 to 8 hours.
  • Must be authorized to work in the United States by any employer; permanent U.S. work authorization is required.

Nice To Haves

  • QC laboratory experience that includes Raman spectroscopy testing.
  • Experience sampling raw materials for GMP operations.
  • Experience with GMP industry standards as applied to raw materials.
  • Experience with LabWare LIMS.

Responsibilities

  • Perform raw material sampling in the GMP warehouse to support clinical and commercial manufacturing operations.
  • Perform daily sanitization of ISO-classified sampling areas.
  • Perform and review appearance, gas, and Raman spectroscopy testing on raw materials.
  • Participate in continuous improvement activities, identify opportunities in sampling areas, and use site continuous improvement tools.
  • Plan and prioritize assignments to meet department and site goals.
  • Record and maintain related data and records in compliance with cGMP and quality procedures.
  • Perform work consistently with company safety policies and procedures.
  • Participate in company culture-based programs.
  • Perform additional tasks as needed in the QC Analytical Department.

Benefits

  • 401(k) plan with Pfizer matching contributions and an additional Pfizer retirement savings contribution.
  • Paid vacation, holidays, and personal days.
  • Paid caregiver, parental, and medical leave.
  • Medical, prescription drug, dental, and vision coverage.
  • Eligibility to participate in Pfizer’s Global Performance Plan, with a bonus target of 7.5% of base salary.
  • Relocation assistance may be available based on business needs and/or eligibility.
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