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QC ANALYST I – RAW MATERIALS

Planet Pharma
Bedford, MA Full Time
POSTED ON 6/2/2026
AVAILABLE BEFORE 7/1/2026
QC Analyst I – Raw Materials

Location: Bedford, Massachusetts

Category: Quality and Compliance

Salary: Apply for details

Country: United States

Employment: Contract

Worksite: On-Site

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Job Description

Target PR Range: 36-46/hr DOE

Role Summary

The QC Analyst I – Raw Materials is responsible for carrying out and coordinating routine raw material sampling activities to support GMP manufacturing. This includes tracking incoming materials, planning sampling, and reviewing and entering external test results into internal systems and maintaining laboratory spaces.

This role requires routine aseptic gowning and entry into classified cleanroom environments to perform raw material sampling activities in accordance with GMP requirements and contamination control procedures. The incumbent ensures sampling activities are performed accurately, compliantly, and on schedule to support manufacturing timelines.

Key Responsibilities

  • Perform routine GMP sample collection, labeling, and chain-of-custody documentation to support timely raw material disposition and release.
  • Coordinate with Warehouse Operations to facilitate sample logistics, including material movement and shipment of samples to designated Contract Testing Laboratories (CTLs).
  • Perform routine cleaning of equipment within GMP cleanroom areas, as well as general laboratory upkeep activities, to maintain inspection-readiness in all QC owned areas.
  • Maintain required qualifications for entry into GMP cleanroom areas, including aseptic gowning and GMP material movement in accordance with site procedures.
  • Serve as a qualified trainer for the Raw Material Sampling Area following a period of sustained positive performance in aseptic gowning practices.
  • Ensure accurate and timely review, reconciliation, and upload of external laboratory results into internal quality systems with assistance from management.
  • Support deviation, investigation, and CAPA activities related to sampling operations as needed, with management guidance and oversight.
  • Support Warehouse operations with material movement activities into GMP cleanroom areas as a secondary responsibility, in accordance with GMP and aseptic handling procedures.

Requirements

  • GMP, pharmaceutical, biotech, or regulated laboratory experience preferred.
  • Hands-on experience or familiarity with raw material sampling and GMP documentation practices preferred.
  • Experience coordinating with QMS Systems (Veeva) and Oracle is a plus
  • Working knowledge of data integrity principles, chain-of-custody expectations, and sample lifecycle management preferred.
  • Strong organizational, communication, and time-management skills working independently after receiving instruction, with the ability to manage multiple priorities in a fast-paced environment following established procedures.
  • Ability to work cross-functionally with QC, Warehouse, Manufacturing, Quality Assurance, and external partners.
  • Experience coordinating with QMS Systems (Veeva) and Oracle is a plus

Physical Demand Requirements

  • Ability to stand for extended periods with periodic stooping, bending, or kneeling.
  • Ability to lift, push, and pull up to 50 lbs.
  • Capability to climb ladders and stairs of varying heights.
  • Work in a laboratory and warehouse-adjacent environment requiring personal protective equipment (PPE) for head, face, hands, feet, and body.
  • Work in temperature-controlled environments, including cold rooms.
  • Must remove make-up, jewelry, and contact lenses when working in clean room-associated spaces.
  • Must successfully complete a vision exam assessing near and mid-range clarity, depth perception, and color differentiation with or without correction.

Equal Opportunity Employer

We are proud to be an equal opportunity employer. We welcome and encourage applications from all qualified candidates regardless of race, sex, gender identity or expression, disability, age, religion or belief, sexual orientation, or any other characteristic protected by applicable laws and regulations. It is our policy not to discriminate against any applicant or employee, and we are committed to fostering a diverse, inclusive, and respectful work environment across all locations in which we operate. We believe that diversity, equity, and inclusion are fundamental to our mission and enhance our ability to serve clients globally. If you have a disability or require any reasonable accommodations during the application or interview process, please inform your recruiter or contact us directly so that we can explore the appropriate arrangements.

Fraud Alert

Candidate safety is a top priority at Planet Pharma. The industry has seen an increase in people falsely representing themselves as recruiters to gather personal information from job seekers. For your safety, do not provide sensitive data to anyone you have not spoken with thoroughly, never provide banking information during the application process and always double check the email address of the Recruiter to ensure it’s from an official Planet Pharma domain (@planet-pharma.com, @planet-pharma.co.uk, and @ppgadvisorypartners.com) and not a domain with an alternative extension like .net, .org or .jobs.
The Planet Group of Companies is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

Salary.com Estimation for QC ANALYST I – RAW MATERIALS in Bedford, MA
$63,072 to $80,303
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