Quality Assurance Validation Contractor

BioPharma Consulting JAD Group

  • Boston, MA
  • 30+ days ago

    Highlights

    Collaborate with cross-functional teams (Validation, QA, Engineering, Manufacturing, QC) to support timely execution of validation projects. Team player who works well in large multi-disciplinary project groups by listening effectively and inviting open discussion.

    Numbers & Facts

    LocationBoston, MA

    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

    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

    Similar Jobs

    See more jobs