With over 15 years of experience in the pharmaceutical and chemical industry as well as in biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated experts who want to develop professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages - completely free of charge. Register with us and reap the benefits of interesting job offers that match your skills and experience. Description • 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 CAPAs • Write and/or revise procedures applicable to the Engineering activities • Support the Engineering group to prepare the validation, requalification, and maintenance program Profile • Education: Bachelors degree in Engineering or technical field • Good English language skills • Prpfound experience in the Pharma industry as a CQV Engineer / Specialist Job Offer • Pleasant working atmosphere • Further training opportunities Reference number : 778863/1