Sterile C&Q Specialist - Onsite Puerto Rico
Listed on 2026-10-06
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Pharmaceutical
Validation Engineer, Pharma Engineer
Legalpmpartners is seeking a Commissioning & Qualification (C&Q) Specialist for a four-month, on-site assignment in Manatí, Puerto Rico. The role focuses on commissioning, qualification, validation, startup, and operational readiness of pharmaceutical equipment and systems, with emphasis on ALM electronic validation.
Responsibilities include developing IQ/OQ/PQ protocols for sterile areas, supporting HVAC, utilities, BAS, autoclaves, and CSV activities, and ensuring documentation
This posting is for the Sterile C&Q Specialist
- Onsite Puerto Rico (4-month) role at Legalpmpartners, based in Houston, TX, United States.
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
Learn more about the Sterile C&Q Specialist
- Onsite Puerto Rico (4-month) role in the description above.
We appreciate your interest in this position.
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