Biopharma C&Q Specialist: Validation & Commissioning

Validation & Engineering Group; Washington (District of Columbia); On-site; USD 90,000 - 150,000; Full time

Job summary

Validation & Engineering Group is seeking C&Q Specialists to support equipment and systems in a biopharmaceutical facility. You will execute field activities, document results, and collaborate with project teams to complete system qualification and turnover.

Responsibilities include developing, reviewing, and executing commissioning and qualification protocols, performing field walkdowns, installation verification and functional testing, and reviewing drawings and vendor documentation against

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

Job description

Validation & Engineering Group is seeking C&Q Specialists to support equipment and systems in a biopharmaceutical facility. You will execute field activities, document results, and collaborate with project teams to complete system qualification and turnover.

Responsibilities include developing, reviewing, and executing commissioning and qualification protocols, performing field walkdowns, installation verification and functional testing, and reviewing drawings and vendor documentation against