Junior Validation Engineer with CSV / CQV
Must-Have Skills:
Experience performing validation and calibration activities for pharmaceutical manufacturing and sterile processing equipment in compliance with GMP and 21 CFR Part 11 requirements.
Hands-on experience supporting Master Validation Plans (MVPs), SOPs, validation protocols, and Process Performance Qualification (PPQ) activities.
Experience executing Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) for manufacturing equipment.
Nice to Have Skills:
Experience with FDA regulations, data integrity, and computerized system validation (CSV).
Familiarity with risk assessments, deviation investigations, CAPA, and change control processes.
#J-18808-LjbffrJunior Validation Engineer with CSV / CQV in cambridge at Unknown Company
This position is listed as full time and onsite.