CQV Engineer

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.

Key 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