Develop and execute commissioning protocols (FAT, SAT, IQ, OQ, PQ).
Lead qualification of equipment, utilities, and facilities in GMP-regulated environments.
Perform risk assessments and ensure compliance with regulatory standards (FDA, EMA, GAMP, ISPE).
Review system documentation (P&IDs, wiring diagrams) and participate in system walkdowns.
Collaborate with engineering, manufacturing, and quality teams to support installation and commissioning.
5+ years of C&Q experience in Pharmaceuticals, Biotech, or Medical Devices.
Strong knowledge of GMP, FDA, EMA, ISPE, and GAMP regulatory requirements.
Hands-on experience with HVAC, bioreactors, clean utilities, process gases, and environmental monitoring systems.
1099 ContractsThe Kerryman Bar & Restaurant is an award winning establishment that has been open in River North for over 20 years. We are now hiring for a part time busser. Candidate must be able to work nights and weekends. The successful candidate should be prepared to work as...