Full-Time

Quality Assurance Validation Contractor

BioPharma Consulting JAD Group

BioPharma Consulting JAD Group

No salary listed

Boston, MA, USA

In Person

Work is onsite in Boston, Massachusetts.

Bachelor's

Category
Biology & Biotech (1)
Required Skills
Veeva
Quality Assurance (QA)
Requirements
  • Bachelor's degree in a technical discipline, or 7+ years of equivalent work experience in lieu of a degree.
  • At least 5 years of validation and/or quality assurance experience, or 7+ years of equivalent work experience without the degree.
  • Knowledge of 21 CFR, International Council for Harmonisation regulations, European Union regulations, GAMP 5, and risk-based validation.
  • Experience applying risk-based decision making in collaborative, multidisciplinary project environments.
Responsibilities
  • Provide quality assurance oversight of commissioning, qualification, and validation activities for the current Good Manufacturing Practice manufacturing facility and quality control laboratories.
  • Provide quality assurance oversight for the periodic review and requalification program.
  • Review computerized maintenance management system records related to asset management, including asset release, database requests, and work orders.
  • Author and review standard operating procedures in Veeva.
  • Review and approve validation protocols and reports, including installation qualification, operational qualification, performance qualification, computer system validation, process validation, and cleaning validation.
  • Ensure validation activities comply with applicable Good Manufacturing Practice regulations, industry guidance, and internal standard operating procedures.
  • Collaborate with Validation, Quality Assurance, Engineering, Manufacturing, and Quality Control teams to support timely execution of validation projects.
  • Participate in change control assessments, risk assessments, and deviation investigations related to validation.
  • Provide quality assurance input during validation planning and execution phases.
  • Support audits and regulatory inspections by providing validation documentation and addressing quality assurance inquiries.
  • Ensure data integrity and documentation accuracy in all validation records.
  • Maintain current validation-related records and documentation.
Desired Qualifications
  • Prior experience working in cell and gene therapy manufacturing.
  • Prior experience working with contract manufacturing.
  • Experience with Kneat.
  • Ability to work effectively in large multidisciplinary project groups by listening effectively and inviting open discussion.
BioPharma Consulting JAD Group

BioPharma Consulting JAD Group

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