As a CSV professional, you will responsible for validation of various computer systems, control systems and processes, and write protocols and reports in collaboration with Validation, Business Process Owner and QA.
Skills: Hands-on experience authoring and executing validation protocols (IQ/OQ/PQ), Trace Matrices, Validation Plans, Validation Final Reports, test plans. Ability to work independently and within project teams, while managing multiple deliverables under tight deadlines.
Minimum Requirements: B.S. in biological sciences, chemistry, or engineering with 3 plus years of manufacturing, engineering or QA/QC experience. Must have a minimum of 3 years direct/hands on experience with the validation of Laboratory systems. Experience of LIMS is required.
DON'T SEE YOUR TITLE HERE, PLEASE SEND YOUR RESUME TO CAREERS@PROVALID8INC.COM AND LET'S CHAT!. We are always looking for candidates who are excited about their work, motivated to do their best and looking for ways to improve.