LL02-250624 Validation Specialist

Validation & Engineering Group, Inc. (V&EG) is a leading service provider offering solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries. Our services include Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and others. We are seeking a talented, dedicated Validation Specialist committed to the highest ethical standards. Qualifications

Bachelor's Degree in Science or Engineering Minimum of 3 years of experience in pharmaceutical, medical device, or biotechnology industries Experience in process/manufacturing areas Fully bilingual in English and Spanish with excellent oral skills Proficient in MS Windows and Microsoft Office Strong knowledge of cGxP and regulatory guidance, with understanding of their application in compliance Experience in Design Documentation (URS, DS), IQ, OQ, PQ protocols, deviations, and reports Knowledge of SDLC, Risk Assessment, Data Integrity, FAT, and SAT Knowledge of medical devices equipment is preferred Technical writing skills and experience in investigation processes Availability to work extended hours, including weekends and holidays Seniority level

Mid-Senior level Employment type

Full-time Job function

Strategy/Planning and Information Technology

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