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Proclinical Logo Proclinical · Quality Control

Quality Control Analyst II

United States, Norton 40.00 - 45.00 USD / Hour · Job Posted January 07, 2026
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Job Description

Quality Control Analyst II - Contract - Norton, MA. Are you passionate about quality and precision? Join our client as a Quality Control Analyst and help ensure top-tier standards every day. Proclinical is seeking a Quality Control Analyst to join a dynamic team in the pharmaceutical/biotechnology industry. Primary Responsibilities: In this role, you will perform analytical and microbiological testing to support raw materials, in-process samples, product release, and stability studies. You will play a key role in maintaining laboratory operations, ensuring compliance with regulatory standards, and contributing to continuous improvement initiatives.

Job Responsibility

  • Conduct routine and non-routine analytical HPLC/UPLC or microbiological assays for various samples
  • Support weekend laboratory operations and maintain accurate training records
  • Adhere to testing schedules and ensure timely completion of assignments to meet project timelines and quality metrics
  • Assist in maintaining laboratory equipment and inventory for smooth operations
  • Submit data promptly and review data as needed to ensure efficiency
  • Perform operational tasks such as critical utility sampling, environmental monitoring, and product testing
  • Contribute to updating controlled documents, including SOPs, work instructions, and test methods
  • Ensure compliance with internal standards, policies, and regulatory guidelines (e.g., GMP, GLP, ICH)
  • Collaborate with QC and cross-functional teams to support quality control operations
  • Participate in inspection readiness activities and support audits and inspections
  • Support continuous improvement initiatives to enhance laboratory efficiency and effectiveness

Requirements

  • Degree in biology, biochemistry, chemistry, or a related scientific field (Associate degree or Biotech Certificate considered)
  • Experience in GMP quality control within the pharmaceutical or biotechnology industry
  • Knowledge of microbiology testing and environmental monitoring/critical utility sampling
  • Familiarity with quality events such as investigations, deviations, CAPAs, and change controls
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