Teams at Miltenyi Biotec

Support biologics manufacturing under cGMP by managing quality events (deviations, CAPAs, change requests), writing and reviewing GMP documentation (SOPs, BPRs), providing floor-level SME support, troubleshooting processes, participating in audits and validation, training junior staff, and driving Lean process improvements to maintain on-time operations and performance metrics.

Support daily GMP laboratory operations including maintaining 5S standards, consumables inventory (Kanban), receiving/distribution, equipment checks, preventive maintenance, calibration scheduling, equipment qualification support (IQ/OQ/PQ), compliance with EHS/GMP/21 CFR Part 11, documentation (SOPs, logs), and continuous improvement initiatives to ensure safe, efficient, and compliant lab workflows.