CQV Specialist (m/f/d)

Ihre Aufgaben:
• Involved in all validation activities including but not limited to: Facilities, Utilities, Validation Life Cycle, Execution, Technical Documentation, Process, GAP Analysis, Risk Assessment, among others
• Involved in the validation documentation including: URS, DQ, FMEA, Risk Assessments, FAT, SAT, Protocols (IQ, IOQ, OQ, PQ)
• Prepare validation documents
• Execution of IQ/OQ and PQ for equipment, systems and utilities
• Write reports of completed validation activities. Work to identify efficiencies in the validation program approach
• Work to apply lessons learned and stay informed of industry regulatory changes as it applies to equipment / facility validation
• Perform assigned Quality Systems activities including Document Management system, Change Control, Non-Conformities, and CAPA’s
• Write and/or revise procedures applicable to the Engineering activities
• Support the Engineering group to prepare the validation, requalification, and maintenance program

Ihre Qualifikationen:
• Education: Bachelor’s degree in Engineering or technical field
• Good English language skills
• Prpfound experience in the Pharma industry as a CQV Engineer / Specialist

Ihre Vorteile:
• Pleasant working atmosphere
• Further training opportunities

Projektdauer: 6 MM


Sie sind Freiberufler? Dann freuen wir uns auf Ihre Bewerbung!