Validation Engineer

Jobtailor; California (MO); On-site; USD 90,000 - 150,000; Full time

Job summary

Jobtailor in the United States seeks a senior CQV specialist to support cleaning validation activities for API and PMO manufacturing.

You will monitor validated systems, plan, write and execute qualification protocols (IQ, OQ, PQ) and reports, conduct investigations, and mentor team members.

The role requires a bachelor’s degree in a science field and 5+ years of CQV experience in GMP/GDP environments.

Qualifications

• Bachelor’s degree in science discipline (chemistry, biochemistry, biology or equivalent).
• 5+ years of Commissioning, Qualification & Validation (CQV) / cleaning validation experience in a GMP/GDP environment.
• Experience with planning, writing and executing qualification protocols (IQ, OQ, PQ) and reports.
• Experience with validation / monitoring of critical pharmaceutical utility systems.
• Understanding of cleaning validation requirements for pharmaceutical industry.

Responsibilities

• Support cleaning validation activities for API and PMO manufacturing
• Monitor facility/utility validated systems, plan, write and execute validation/qualification protocols
• Conduct related investigations
• Train, coach and mentor team members

Education

Bachelor’s degree in science discipline (chemistry, biochemistry, biology or equivalent)

Job description

Responsibilities

• Support cleaning validation activities for API and PMO manufacturing
• Monitor facility/utility validated systems, plan, write and execute validation/qualification protocols
• Conduct related investigations
• Train, coach and mentor team members

Requirements

• Bachelor’s degree in science discipline (chemistry, biochemistry, biology or equivalent)
• 5+ years of Commissioning, Qualification & Validation (CQV) / cleaning validation experience in a GMP/GDP environment
• Experience with planning, writing and executing qualification protocols (IQ, OQ, PQ) and reports
• Experience with validation / monitoring of critical pharmaceutical utility systems
• Understanding of cleaning validation requirements for pharmaceutical industry