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Salary
≈ $71k – $177k per year (Estimated)
Location
In office (Boston)
Employment
Contractor

Confirmed on the employer's own hiring board on Sep 27, 2026. First seen by Alion on Aug 25, 2026.

Overview
Company
Impact
Profile match
BioPharma Consulting JAD Group is a technical consulting and staffing firm based in Carolina, Puerto Rico, that provides quality, engineering, validation, commissioning and regulatory compliance professionals to FDA-regulated pharmaceutical and biotechnology manufacturers. Founded in 2010, it has business locations in Massachusetts, Texas, California, Florida and Puerto Rico, and places consultants at client manufacturing sites such as those in Juncos, Puerto Rico and the Boston area. It recruits manufacturing specialists, process, reliability, maintenance and plant engineers, QA specialists, operational quality managers and process development scientists for client assignments.

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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