What are the responsibilities and job description for the Validation Engineer position at Redbock - an NES Fircroft company?
A large pharmaceutical company in Los Angeles is in immediate need of a CQV Engineer for a 12-month project, this is an onsite position and is 40 hours/week.
The client needs someone with Facilities CQV experience including EMPQ, Vessel IOV and IOPQ including mixing and temp mapping. They have personnel assigned to Utilities (WFI, Alcohol, N2, Compressed Air, etc.), CIP, Filter Press, Centrifuge, CIP skids and Cleaning Validation; this experience is preferred in case they need additional support. The project also requires daily job walks of the construction site daily in full PPE.
Top Requirements:
- BS degree minimum
- 3-10 years of Validation Engineering experience in pharmaceutical industry
- Strong skill set in installation and IQOQ of equipment like centrifuges, filter presses, and processing tanks
- Cleanroom qualification experience is a plus
- Very strong technical writing/documentation skills
- Very strong communication skills and ability to coordinate with cross-functional teams
- Experience doing job walks with engineers for capital projects
- Must have a positive attitude and ability to multi-task
- Must be committed to supporting a long-term project that could go for 2 years
- Must be available to support other shifts as requested by the client, this could happen on short notice