What are the responsibilities and job description for the Validation Specialist position at Intellectt Inc?
Role: CQV Associate
Location: Los Angeles, CA - Onsite
Duration: 12 Months
W2/1099 - No C2C
Our client is seeking a Validation Engineer with Facilities CQV experience, specifically in EMPO, Vessel IOV, and IOPQ, including mixing and temperature mapping. While their team has personnel assigned to Utilities (WFI, Alcohol, N2, Compressed Air, etc.), CIP, Filter Press, Centrifuge, CIP skids, and Cleaning Validation, experience in these areas is preferred to provide additional support if needed. The role also requires daily job walks of the construction site in full PPE.
Top Requirements:
- BS degree minimum
- 1–4 years of Validation Engineering experience in the pharmaceutical industry
- Strong expertise in installation and IQOQ of equipment such as centrifuges, filter presses, and processing tanks
- Exceptional technical writing and documentation skills
- Excellent communication skills with the ability to coordinate with cross-functional teams
- Experience conducting job walks with engineers for capital projects
- Positive attitude and ability to multi-task
Additional Preferred Experience:
- Qualification of cleanroom facilities and large process equipment (Vessels, Centrifuges, Filter Presses, and CIP skids)
- Execution of EMPO, Vessel IOV, and IOPQ protocols, including mixing and temperature mapping
- Experience writing and executing protocols and final reports
If you are seeking any other roles in the Life Science/Manufacturing/Automotive Industry please do share your resume to eswar@intellectt.com - No C2C Enquiries please
