Description
• Quality Assurance Documentation (e.g. Batch Records, Raw Material Records, Solution Preparation Records, etc.).
• Filing Quality Assurance Documentation (e.g. Batch Records, Raw Material Records, Solution Preparation Records, etc.).
• Binding of Quality Assurance Batch Records.
• Additional Administrative duties as required per Quality Assurance Management.
• Escalating detected major issues to QA Management related to role responsibilities.
Additional Skills & Qualifications
• 1 year experience in Quality Assurance Documentation
• Experience in a regulated/GMP, Pharmaceuticals or Biotechnology preferred.
• Understanding of 21 CFR 210, 21 CFR 211, and ICH Q7 regulations preferred.
• Ability to work in a fast-paced environment.
• Ability to adapt to changing priorities and timelines.
• Ability to build positive working partnerships with other department teams.
Job Type & Location
This is a Contract position based out of Milford, M...