Pharmaceutical Process Engineer
4 days ago
VTI Life Sciences is currently seeking a skilled CQV Engineer to join our team in the Greater Los Angeles area. The successful candidate will be responsible for supporting engineering and CQV activities related to the project expansion at our client's pharmaceutical facility.
Key ResponsibilitiesThe CQV Engineer will be responsible for generating User Requirement Specifications, Functional Specifications, Design Specifications, SOPs, Management of Change (MOC), supporting FMEA activities, HAZOP processes, performing Risk Assessments, Gap Assessments, project closeout documentation, turnover package generation, project change requests, and supporting client and A/E firm in project design.
Technical Requirements- Minimum of 5 years of experience in Project Engineering and Validation for Pharmaceutical process equipment and instrumentation.
- Knowledge of cGMP and other regulatory standards.
- Proficiency in Project Engineering and construction-related activities.
- Experience with Equipment, Process, Cleaning, Facility, and Software Validation.
At VTI Life Sciences, we value our employees and offer a competitive salary range of $95,000 - $120,000 annually for a W2 employee, along with excellent benefits, 401K, and a stimulating work environment that values trust, respect, openness, teamwork, creative talent, enthusiasm, and diligence. As a leading global Commissioning, Qualification, and Validation Services organization, VTI Life Sciences is always looking for innovative, talented, and experienced validation professionals for our multinational and global offices.
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