Senior Technician, Quality Assurance

Role: Senior Technician in Quality Documentation at an animal health vaccine manufacturing site, supporting GMP compliance and document control for biologics production including fermentation and cell culture. Responsibilities: maintain and revise quality systems documentation such as SOPs, batch records, and forms; ensure documentation adheres to GMP and regulatory standards; support change control activities; assist audits and inspections; manage electronic document systems; collaborate with manufacturing, QA, QC, and technical teams; monitor process metrics and identify improvements. Requirements: high school diploma with 5+ years relevant experience or AS/BS in a related field; strong organizational, communication, and MS Office skills; ability to work independently and in teams; familiarity with GMP, regulated manufacturing, and document control preferred. HighValue: biologics manufacturing, vaccine production, GMP environment, document control, compliance, regulated biotech manufacturing. WorkSetup: on-site in Worthington, MN; travel approximately 10%.