Commissioning & Qualification Engineer supporting qualification activities for laboratory equipment at a pharmaceutical company. Leading compliance with cGMP regulations in a regulated laboratory environment.
Responsibilities
Support qualification activities for laboratory equipment
Lead Commissioning & Qualification activities
Develop and execute Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) protocols
Perform impact assessments and risk assessments
Ensure compliance with cGMP regulations and FDA guidelines
Author and review validation documentation
Collaborate with Quality Assurance, Engineering, Validation, and Laboratory teams
Requirements
Bachelor’s Degree in Engineering, Chemistry, Microbiology, or a related scientific discipline
3+ years of experience in commissioning, qualification, or validation within pharmaceutical, biotechnology, or medical device industries
Strong understanding of cGMP and FDA regulations
Experience generating and executing IQ, OQ, and PQ documentation
Strong technical writing and documentation skills
Experience working under FDA, EMA, or other regulatory inspections
Familiarity with ASTM E2500 risk-based validation approaches
Knowledge of 21 CFR Part 11 and data integrity requirements
Benefits
Health insurance
Dental insurance
Vision insurance
Paid time off
Educational assistance
401(k) retirement plan
Flexible work arrangements
Professional development resources
Employee resource groups
Volunteer activities
Job title
Commissioning and Qualification (C&Q) Engineer – Laboratory Equipment
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