C&Q Inspection Engineer
Our team is looking for a highly skilled CQV testing professional to develop and execute comprehensive inspection systems documentation, ensuring GMP compliance and meeting key project deliverables for safety, schedule, and quality of project-related documentation/electronic records.
* Develop and execute test plans for inspection equipment in Sterile Drug product facilities.
* Ensure strict adherence to EU & FDA regulations.
* Implement deviation management strategies for assigned equipment and utilities.
Key Requirements:
* Bachelor's degree in a scientific, technical, or engineering discipline.
* Minimum 5 years of experience within the pharmaceutical industry with demonstrable capacity to execute CQV testing approaches from initiation to completion.