Biopharma C&Q Specialist - Field Validation & Turnover

Veg Group; Humacao (PR); On-site; USD 90,000 - 140,000; Full time

Job summary

Validation & Engineering Group, Inc. is 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. Ideal candidates have 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, and a working knowledge of GMP requirements

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.

Responsibilities

• 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.

Skills

C&Q Expertise

GMP Knowledge

Job description

Validation & Engineering Group, Inc. is 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. Ideal candidates have 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, and a working knowledge of GMP requirements