Lexington, KY30+ days ago
Qualifications & Requirements - Bachelor of Science in Engineering.- 0-2 years of relevant experience.- Experience in Pharmaceutical, Biotech, Medical Device Design, Construction, Commissioning, Validation, or- QA.Preferred Qualifications- Experience in writing and execution of PFC, FC, IQ, OQ, and PQ forms/protocols for GMP Utilities, Equipment, Systems, and Software.- General exposure and experience in a GMP/Validation discipline with a knowledge and understanding of pharmaceutical Design/Build/Commission/Validate processes and how they relate to regulatory requirements and cGMP regulations within the E.U. and U.S. FDA.Physical Demands- Must be able to: stand, sit, and walk for prolonged periods, stoop, kneel, crouch, and crawl as required.- Job Description At IPS, we are global leaders in developing innovative solutions for the consulting, architecture, engineering, project controls, procurement, construction management, and CQV of technically complex facilities, primarily in the life sciences industry.