Manufacturing and Process Engineer
Why This Role Stands Out
This hybrid role offers a fantastic opportunity to grow your expertise in GMP validation and equipment qualification, contributing to critical remediation programs within a reputable company. You'll thrive here if you're a mid-senior level engineer with a knack for detailed protocol development, execution, and cross-functional collaboration, so definitely consider applying to advance your career!
Quick Overview
Job Description
Role and responsibilities:
We are seeking consultants experienced in equipment qualification and GMP validation activities to support remediation and requalification programs.
Key responsibilities:
- Lead and execute equipment requalification activities.
- Prepare and review qualification protocols and reports.
- Perform IQ/OQ/PQ activities.
- Support CQV execution across production and utility systems.
- Manage deviations and CAPA linked to qualification activities.
- Ensure GMP compliance throughout the equipment lifecycle.
- Collaborate with Engineering, Manufacturing and Quality teams.
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