Job Description
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.
Skills
Document control, Gmp, Batch record, Capa, Batch record review, Quality assurance
Top Skills Details
Document control,Gmp,Batch record,Capa,Batch record review
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 c...
• 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.
Skills
Document control, Gmp, Batch record, Capa, Batch record review, Quality assurance
Top Skills Details
Document control,Gmp,Batch record,Capa,Batch record review
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 c...
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