Jobs at Bimeda

Leads pharmaceutical quality assurance systems, compliance, audits, inspections, CAPAs, investigations, complaints, product release, and regulatory readiness. Manages QA Associates, customer quality requests, quality metrics, continuous improvement, budgets, and cross-functional resolution of quality events. Requires regulated pharmaceutical QA/QC experience, leadership capability, scientific education, and strong knowledge of cGMP, quality systems, regulatory affairs, and stability protocols. The role is based in-office in a warehouse and production environment with occasional weekend or after-hours work.

The QA Associate manages pharmaceutical GMP quality activities, including batch record review, product release, change control, APRs, deviations, CAPAs, complaints, OOS investigations, audits, and inspection readiness. The role supports implementation of e-QMS, LIMS, and electronic batch records; uses quality metrics and trend analysis; improves SOPs and processes; trains manufacturing personnel; and collaborates with Manufacturing, QC, Regulatory, and customer-facing teams.