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Quality Assurance Validation Contractor

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Onsite

Quality Assurance Validation Contractor

BioPharma Consulting JAD Group

Quality Assurance Validation Contractor

Skills

Testing & QACompliance

2 months ago

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Important information


Contract type:

Freelance / Contract

Location:

Boston, MA, USA

Work mode:

Onsite

Published on:

25 August 2026

What they need


We are looking for Quality Assurance Validation contractors to join our growing QA Validation group in Boston MA.  Positions range from 6 to 12 months. The roles are expected to be onsite in Boston, MA.

Responsibilities:

  • Provide QA oversight of CQV activities for the cGMP manufacturing facility and quality control laboratories.

  • Provide QA oversight for periodic review and requalification program.

  • Perform review of CMMS records related to asset management including asset release, database requests, and work orders.

  • Author and perform review of SOPs in Veeva.

  • Review and approve validation protocols and reports (IQ, OQ, PQ, CSV, process validation, cleaning validation).

  • Ensure compliance of validation activities with applicable GMP regulations, industry guidance, and internal SOPs.

  • Collaborate with cross-functional teams (Validation, QA, Engineering, Manufacturing, QC) to support timely execution of validation projects.

  • Participate in change control assessments, risk assessments, and deviation investigations related to validation.

  • Provide QA input during validation planning and execution phases.

  • Support audits and regulatory inspections by providing validation documentation and addressing QA-related inquiries.

  • Ensure data integrity and documentation accuracy in all validation records.

  • Maintain cu

Requirements

  • Bachelor’s degree in a technical discipline with 5+ years validation and/or quality assurance experience. In lieu of degree, 7+ years of equivalent work experience is required.

  • Knowledge of 21 CFR, ICH, EU Regulations, GAMP 5, risk-based validation.

  • Prior experience working in cell and gene therapy manufacturing preferred.

  • Prior experience working with contract manufacturing preferred.

  • Experience with Kneat strongly preferred.

  • Applies collaborative approach to problem solving and is experienced with risk-based decision making.

  • Team player who works well in large multi-disciplinary project groups by listening effectively and inviting open discussion.

Benefits

  • 6-12 month contract with possible extension
  • administrative shift

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