Job information
About this opportunity
Quick summary
activities within a GMP-regulated environment.Working within a growing site organization, the QC Specialist II will support the transfer, qualification, validation, and lifecycle management of analytical methods used to test pharmaceutical raw materials, in-process materials, finished products, and stability samples. The role will also provide technical leadership in troubleshooting, analytical investigations, equipment qualification, and training activities while partnering across Quality, Manufacturing, MS&T, Engineering, and Validation teams.This is an exciting opportunity to help build the technical capabilities, laboratory systems, and quality infrastructure required to support the continued growth of the Morrisville manufacturing site.
Listing details
- Employer
- Novartis
- Location
- Morrisville, US
- Structured address
- Morrisville, US
- Category
- Engineering
- Base salary
- Not disclosed
- Valid through
- Check official source
- Reference
- REQ-10085045