Biopharma C&Q Specialist – Systems Validation

Veg Group; Barceloneta (PR); On-site; USD 90,000 - 130,000; Full time

Job summary

Validation & Engineering Group, Inc. (V&EG) is a leading services supplier to the pharmaceutical, biotechnology, and medical devices industries in labs, compliance, engineering, and project management.

We are seeking C&Q Specialists to support equipment and systems in a biopharmaceutical facility, executing field activities and documenting results as part of project teams. Ideal candidates have 5+ years of C&Q experience, familiarity with FAT/SAT/IQ/OQ, and strong GMP knowledge.

Qualifications

• At least 5 years of C&Q experience in a pharmaceutical or biopharmaceutical facility.
• Experience with FAT, SAT, IQ, OQ, or comparable commissioning activities.
• Working knowledge of GMP requirements and controlled documentation.
• Strong field execution, documentation, 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

Field execution

Technical writing

Teamwork

Job description

Validation & Engineering Group, Inc. (V&EG) is a leading services supplier to the pharmaceutical, biotechnology, and medical devices industries in labs, compliance, engineering, and project management.

We are seeking C&Q Specialists to support equipment and systems in a biopharmaceutical facility, executing field activities and documenting results as part of project teams. Ideal candidates have 5+ years of C&Q experience, familiarity with FAT/SAT/IQ/OQ, and strong GMP knowledge.