What are the responsibilities and job description for the Sr. CQV Specialist position at Fourways Consulting Services?
Hiring: Sr. CQV Specialist (2 Openings)
Raritan, NJ (100% Onsite)
Long-Term Contract (2 Years)
Looking for professionals with:
8 years of CQV/Validation experience
GMP Pharma, Biotech, or Cell Therapy background
Process Equipment, QC Equipment & Facilities Validation
Smoke Studies, Cleanroom Qualification
USP <1058> & GAMP 5 expertise
Validation Plans, Protocols, IQ/OQ/PQ Execution
Deviation Investigations & Risk Assessments
Salary : $50 - $60