We are seeking
C&Q Specialists to support equipment and systems in a biopharmaceutical facility. The specialists will execute field activities, document results, and work with project teams to complete system qualification.
Description: - Develop, review, and execute commissioning and qualification protocols.
- Perform field walkdowns, installation verification, and functional testing.
- Review drawings, specifications, and vendor documentation against installed systems.
- Document test results, investigate discrepancies, and support corrective actions.
- Coordinate with Engineering, Operations, and Quality to complete qualification and system turnover.
Qualifications: - At least 5 years of C&Q experience in a pharmaceutical or biopharmaceutical facility.
- Experience with FAT, SAT, IQ, OQ, or comparable commissioning and qualification activities.
- Working knowledge of GMP requirements and controlled documentation.
- Strong field execution, technical writing, and teamwork skills.
At Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.
Excited to build something meaningful together? We look forward to hearing from you.
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