New Milford, CT
Our client is a small CMO that works directly with large global providers to small emerging players in the pharmaceutical and medical device sectors. They are currently looking for a Validation Consultant to provide day-to-day validation support from a manufacturing perspective.
Day to Day Responsibilities:
This candidate will come from a Pharmaceutical/Medical Device background with aseptic process validation experience. This individual will be a hands-on Validation Engineer, responsible for writing and executing Validation protocols for the client’ s Manufacturing aseptic fill-line. The client recently introduced a new aseptic process on the manufacturing floor and the line must be completely re-validated. As such, the candidate should have strong cGMP experience, and will be up to date on all the associated FDA regulatory requirements. The candidate will work in a hands-on capacity, driving validation in the upstream and downstream manufacturing areas. This individual should be comfortable on the manufacturing floor, and the ideal candidate will have direct Manufacturing Validation experience in both the Medical Device and Pharmaceutical space.
- Pharmaceutical/Medical Device
- Validation Engineer
- asepticManufacturing Fill-Line Validation
- Writing & Executing Protocols