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Your impact
The Sr. CQV Engineer will be responsible for leading the efforts for commissioning, qualification, and validation of equipment/ systems, and processes in the production of Drug substances/ Drug Product/ Sterile Facilities/ API/ OSDs, as well as the Utility system, HVAC system and Area.
The role will require the leadership of an experienced, energetic, and committed Senior CQV person with broad experience in C&Q;, particularly biopharmaceuticals.
The person should have experience of leading a team of CQV engineers for a project and managing the C&Q; documentation and execution lifecycle from SLIA generation through to OQ completion. The lead will work closely with cross-functional teams, including engineering, quality assurance, and manufacturing,
to support the successful delivery of projects.
Key Responsibilities
Lead and coordinate CQV projects, ensuring timely execution and compliance with industry regulations.
To prepare C&Q; plans in line with the strategic goals of the client and manage timely and compliant delivery of the plan.
Ensure all commissioning and qualification procedures are implemented and adhered to at office and at site level.
Track progress of C&Q; activities as required and provide regular project updates and status reports to stakeholders.
Ensure effective resource planning, including coordinating materials, spares and consumables for commissioning and qualification activities.
Identify and mitigate project risks while ensuring project deliverables meet required quality and compliance standards.
Provide leadership in team meetings and facilitate problem-solving discussions to ensure project milestones are met.
📌 Senior CQV Engineer (India)
🏢 Jacobs
📍 India