×
Register Here to Apply for Jobs or Post Jobs. X

Quality Assurance Validation Contractor

Job in Boston, Suffolk County, Massachusetts, 02298, USA
Listing for: Biopharma-Consulting-Jad-Group
Contract position
Listed on 2026-07-15
Job specializations:
  • Quality Assurance - QA/QC
    Quality Engineering, Regulatory Compliance Specialist, QA Specialist - Analyst/Manager, Quality Control - QC Analysts/Managers
Salary/Wage Range or Industry Benchmark: 60 - 90 USD Hourly USD 60.00 90.00 HOUR
Job Description & How to Apply Below

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
Qualifications
  • 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.
Contract Details
  • 6-12 month contract with possible extension
  • administrative shift
#J-18808-Ljbffr
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)
0
200
Filters
Education Level
Experience Level (years)
Posted in last:
Salary