Seeking a seasoned CQV professional with 10+ years of equipment experience in large-scale biopharmaceutical projects. Must be an SME on CIP systems with a minimum of 5 years of specific CIP experience. Strong communication skills required for interfacing with multiple departments and leading project tasks.
Key Responsibilities
Oversee CQV processes for all CIP equipment.
Review and approve design deliverables, generate CQV documentation, and lead vendor package reviews.
Conduct field walkdowns, manage construction readiness, and execute commissioning and start-up.
Collaborate with various project groups to ensure project lifecycle management.
Must-Have Skills
10+ years of equipment experience in biopharmaceutical manufacturing.
5+ years on Equipment CQV Team.
Proficiency with ASTM E2500 and verification processes.
Experience with complex projects in operational facilities.
Strong liaison abilities with departments and project leads.
Seniority level
Mid-Senior level
Employment type
Full-time
Job function
Engineering and Information Technology
Industries
Staffing and Recruiting
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