Teva Pharmaceuticals has been developing and producing medicines to help improve people’s lives for more than a century. We are committed to being a global leader in generic and specialty medicines with a portfolio of 3,500 products in nearly every therapeutic area. Around 200 million people around the world take a Teva medicine every day. They are served by one of the largest and most complex supply chains in the pharmaceutical industry. Along with our established presence in generics, we have significant innovative research and operations supporting our growing portfolio of specialty and biopharmaceutical products. Learn more at http://www.tevapharm.com.
Teva is Hiring
- Role: Sr. Manager
- Department: QA- Plant, API
- Location : Gwailor, MP
- Experience: 15+ years
Main Responsibilities:
1. Ensure Review of all documentation (i.e. batch records, test results, deviation, LIR, OOS, CAPA, validation, COA, Change Controls, etc.) and perform disposition (release or rejection) of batch.
2. Ensure Review of step-by-step performance and compliance to batch manufacturing and packaging record requirements and resolution of any errors/deviations identified.
3. Development of corrective and preventive actions (review, approval, and on time closure of the CAPA) in order to resolve an event. Ensuring Process/documentation (i.e. Protocol/report) of reviewing effectiveness to determine the effectiveness of a corrective or preventive action.
4. Ensuring and performing investigation into a product quality complaint with resolution including corrective and preventive actions and closure of the investigation.
If you are interested, send me updated CV
Email id : apeksha.shinde@teva.co.in
