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Quality Assurance Validation Contractor

BioPharma Consulting JAD GroupBoston, Massachusetts🇺🇸United StatesPosted Aug 25, 2026

Why This Role Stands Out

This contract role offers a fantastic opportunity to contribute to critical quality assurance validation projects within a respected biopharma consulting group, ideal for experienced QA professionals seeking impactful, project-based work. You'll develop your skills by providing oversight for diverse validation activities and collaborating with cross-functional teams, making this an excellent step to advance your career. Apply today to join a dynamic team and leverage your expertise in a challenging yet rewarding environment.

Quick Overview

Seniority
Mid Senior
Employment type
Temporary/Casual
Work mode
On Site
Location
Boston, Massachusetts, United States
Posted
3 weeks ago
Compliance

Job Description

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

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