Job Summary
This position involves collaborating with a Pharmaceutical client to support project scoping, commissioning, qualification, validation and start-up operations. The role is a 12-month contract and will be fully onsite.
Key Responsibilities
* Generate, review, and execute C&Q documentation for the company and vendors.
* Collaborate with system owners, QA, and stakeholders.
* Oversee and coordinate all C&Q activities for various systems, ensuring compliance with GMP and safety standards.
* Manage C&Q schedules, track status, report risks/issues, and coordinate daily meetings.
* Provide technical support for investigations and system design.
* Assist in the development of URS and QRAES.
Requirements
* 6+ years in Engineering or C&Q management.
* Technical qualification in Engineering or equivalent.
* Extensive C&Q experience in pharmaceutical/biotech projects.
* Strong knowledge of GMP, safety, and environmental regulations.
* Excellent communication, leadership, and collaboration skills.
* Familiarity with paperless validation systems.