C&Q Specialist

Qualifications

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

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.

Benefits

• Collaborative work environment with cross-functional teams.
• Opportunities for professional development and skill enhancement.
• Engagement in critical projects within the pharmaceutical sector.