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Quality Control Analyst

Job in Norton, Bristol County, Massachusetts, 02766, USA
Listing for: Planet Pharma
Full Time position
Listed on 2026-01-02
Job specializations:
  • Quality Assurance - QA/QC
    Data Analyst
  • Healthcare
    Data Scientist
Salary/Wage Range or Industry Benchmark: 37 - 42 USD Hourly USD 37.00 42.00 HOUR
Job Description & How to Apply Below

This range is provided by Planet Pharma. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$37.00/hr - $42.00/hr

Direct message the job poster from Planet Pharma

This is an onsite role in Norton, MA; weekend coverage is required. First shift, Friday-Monday (4 x 10 hours), with initial Monday-Friday training.

The Quality Control Operations (QCO) Analyst II Contractor supports maintaining high standards of quality and compliance from development through commercialization. The role includes performing routine and non-routine testing, participating in data trending, investigations, and lab operations, and supporting method transfers, qualification/validation, verification, and implementation. This position enhances QC efficiency and effectiveness.

Key Responsibilities
  • Perform routine/non-routine analytical (HPLC/UPLC) and/or microbiological assays for raw materials, in-process samples, product release, and stability studies following SOPs.
  • Support weekend lab operations and maintain training records.
  • Assist in lab equipment and inventory maintenance, including reagent and sample prep; review data timely and qualify as a data reviewer.
  • Perform operational assignments (raw material processes, environmental monitoring, in-process testing).
  • Contribute to updating controlled documents (SOPs, work instructions, test methods).
  • Follow internal policies, SOPs, and regulatory standards (GMP, GLP, ICH).
  • Participate in continuous improvement initiatives and cross-functional collaboration.
  • Support regulatory submissions, inspection readiness, and audits.
Qualifications
  • B.S. in chemistry, biology, biochemistry, or related field; 4-8 years of pharmaceutical/biotech experience in GMP QC or equivalent.
  • Experience in method transfer/implementation; understanding of method lifecycle management preferred.
  • Strong technical writing, data analysis, problem‑solving, and organizational skills.
  • Excellent communication and teamwork.
  • Proficiency in Lab Ware LIMS, Excel, Word, and PowerPoint preferred.
Seniority level
  • Associate
Employment type
  • Contract
Job function
  • Quality Assurance, Research, and Science
  • Industries:
    Staffing and Recruiting, Biotechnology Research, and Pharmaceutical Manufacturing

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