Job Description
📋 Description Lead commissioning, qualification, and start-up across facilities, utilities, equipment, and Develop strategy and execute HAZOP studies for capital programs. Plan commissioning/start-up strategies, schedules, protocols, and turnover packages. Ensure systems readiness for GMP operations per regs, quality, safety, standards. Collaborate with engineering, validation, manufacturing, quality, EHS, automation, PM and Manage risks, timelines, budgets, and issue resolution through project lifecycles. 🎯 Requirements Bachelor’s in Engineering, Pharma or Life Sciences; advanced degree preferred. 20+ years in pharma/biotech manufacturing or regulated environments. Experience in commissioning, qualification, start-up, validation, or readiness. Proven cross-functional leadership and matrixed work experience. Strong GMP track record, project leadership, and communications skills. Ability to influence across functions and business units. 🎁 Benefits Comprehensive benefits package including PTO and health insurance. Eligible for long-term incentive programs. Pay range is disclosed; compensation may vary by location and other factors.
