CQV Engineer

Seeking experienced Commissioning & Qualification (C&Q) Engineers to support a major pharmaceutical packaging expansion project involving four new secondary and tertiary packaging lines. This is a true hands‑on C&Q role focused on commissioning, system turnover, equipment verification, and GMP readiness within a regulated manufacturing environment. Validation‑focused profiles will not be considered.

• Strong hands‑on Commissioning & Qualification (C&Q) experience in pharmaceutical manufacturing environments
• Experience supporting packaging equipment commissioning and system turnover
• Expertise in commissioning protocols, test scripts, punch lists, and turnover packages
• Experience with SAT (Site Acceptance Testing) activities
• Knowledge of FDA, GMP, and regulated pharmaceutical operations
• Hands‑on equipment walkdowns, system verification, and commissioning checks

• Execute commissioning and qualification activities for new packaging equipment installations
• Develop, review, and execute C&Q documentation and commissioning protocols
• Perform equipment walkdowns, functional verifications, and commissioning checks
• Manage punch list tracking, issue resolution, and system turnover activities
• Support SAT execution and ensure equipment readiness for GMP operations
• Coordinate with cross‑functional teams to ensure systems meet design and operational requirements
• Maintain accurate C&Q documentation and compliance records