Teams at Bimeda

Supports vaccine manufacturing by preparing, labeling, packaging, and cleaning production areas and equipment. Maintains accurate temperature and process records, reports equipment malfunctions, follows GMP, SOPs, and safety procedures, assists with warehouse tasks, monitors frequently used inventory, and helps maintain organized production areas. This is a part-time role requiring 15–20 hours weekly and Tuesday and Thursday morning availability.

The QA Associate supports pharmaceutical manufacturing quality systems and continuous improvement. Responsibilities include deviation, complaint, and OOS investigations; batch record review and product release; incoming packaging inspections; internal audits; SOP development; GMP compliance; audit support; laboratory testing coordination; and corrective action follow-up. The role also trains manufacturing personnel, monitors quality metrics, resolves compliance issues, and collaborates with production, vendors, and cross-functional teams.

Lead QA systems and a team to ensure product quality and regulatory readiness. Manage audits, investigations, CAPAs, customer complaints, KPIs, and cross-functional corrective actions to maintain cGMP/QSR/GDP compliance and support product release.