C&Q Engineer
About The Position
We are looking for an experienced Commissioning & Qualification (C&Q) Engineer to join our team in support of a major capital expansion project involving the installation of four new packaging lines. This is a hands-on C&Q role embedded within a pharmaceutical secondary and tertiary packaging operation for final drug product. This is not a validation role—we are looking for a true C&Q professional with deep expertise in equipment commissioning, system turnover, and manufacturing process knowledge within a regulated pharmaceutical environment. You will be responsible for leading and executing commissioning and qualification activities across new packaging equipment installations, ensuring all systems are built, installed, and functionally verified to specification and ready for handover to GMP manufacturing operations.
Requirements
- Experienced Commissioning & Qualification (C&Q) Engineer
- Deep expertise in equipment commissioning
- Deep expertise in system turnover
- Deep expertise in manufacturing process knowledge within a regulated pharmaceutical environment
- Experience in leading and executing commissioning and qualification activities
- Experience with commissioning plans, commissioning protocols, test scripts, punch lists, and turnover packages
- Experience with hands-on equipment walkdowns, system verifications, and commissioning checks
- Experience managing punch list identification, tracking, and resolution
- Experience collaborating with equipment vendors, engineering, construction, and operations teams
- Experience supporting and executing SAT (Site Acceptance Testing)
- Knowledge of FDA, GMP, and applicable site and regulatory standards
- Ability to apply manufacturing process knowledge to ensure commissioning scope and acceptance criteria reflect real-world operational requirements
- Ability to maintain accurate and complete C&Q records in compliance with site documentation standards and data integrity requirements.
Responsibilities
- Lead and execute commissioning and qualification activities for new secondary and tertiary packaging equipment installations across four new packaging lines in Building 2
- Develop, author, review, and execute C&Q documentation including commissioning plans, commissioning protocols, test scripts, punch lists, and turnover packages
- Perform hands-on equipment walkdowns, system verifications, and commissioning checks directly on the manufacturing floor
- Manage punch list identification, tracking, and resolution through to system acceptance and turnover
- Collaborate with equipment vendors, engineering, construction, and operations teams to ensure systems are installed, functional, and commissioned to design specification
- Support and execute SAT (Site Acceptance Testing) activities for incoming packaging equipment
- Ensure all C&Q activities are performed in compliance with FDA, GMP, and applicable site and regulatory standards
- Apply manufacturing process knowledge to ensure commissioning scope and acceptance criteria reflect real-world operational requirements
- Partner with Quality, Manufacturing, and Engineering to support a clean, compliant turnover of commissioned systems into GMP operations
- Maintain accurate and complete C&Q records in compliance with site documentation standards and data integrity requirements.
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What This Job Offers
Job Type
Full-time
Career Level
Senior
Education Level
No Education Listed
