What are the responsibilities and job description for the 0020V Lead Cleaning Validation Engineer position at Two River Consulting Partners?
0020V Lead Validation Engineer (Pharma) Please contact Amanda Mazza, amanda@tworivercp.com**Cleaning Validation SME***SUMMARYThe New Product Introduction (NPI) project aims to implement facility modifications for the tech transfer of one or more new products into the LSCC as well as further improvements that may be used to drive future enhancements in manufacturing throughput. The selected candidate will lead the CIP / SIP portion of the NPI project.Mandatory Requirements: 7-10 years of relevant Validation Experience within pharma / biologics.Minimum 5 years of Cleaning Validation experience to include:1. Hands-on experience taking rinse and swab samples and performing visual inspection.2. Experience developing CIP and SIP cycles for process piping, transfer panels, and bioreactors.3. Experience developing load patterns for autoclaves and parts / glass washers.4. Experience with Delta V automation for CIP / SIP.5. Hands on experience executing Riboflavin studies. Preferred Requirements to include:1. Experience using Ellab ValSuite Pro system2. Experience using Valgenesis for electronic development/review of protocols and execution. LOCATIONOn-site in Devens, MAEMPLOYMENT January 1, 2026 start date – 1 year assignment potential extension- Competitive C2C Powered by JazzHRlEgKr2GLij