About this role
CQV Engineer at ELIQUENT Life Sciences. Location: Indianapolis, Indiana, United States. Role: writing documents, executing validations, performing mapping Requirements: Bachelors in engineering/science or equivalent experience; 2+ years validation experience in regulated manufacturing (biotech/pharma/medical device); writing validation documents; FAT/SAT/IQ/OQ/PQ; temperature mapping; FDA and cGMP knowledge; P&ID interpretation. Category: Engineering Seniority: Entry Level Commitment: Full Time Workplace: Onsite Languages: English