Teva is a global pharmaceutical leader and the world’s largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide. Our employees are at the core of our success, with colleagues in over 80 countries delivering the world’s largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and we’ve built a promising pipeline centered around our core therapeutic areas.
Job description
Roles and Responsibilities
1. Analysis of Solid oral dosage i.e. Dissolution, Assay, CU, BU and Related substances etc.
2. Analysis of samples received from Formulation department (samples include in-process, finished product, pre-formulation study samples and stability samples etc.).
3. To carry out analytical method development, in-process samples and finished products.
4. To carry out analytical method transfer activity to QC, Goa.
5. Trouble shooting of analytical instruments for difficulties faced during day-to-day operations.
6. Laboratory compliance and data integrity during day-to-day operations.
7. To prioritize and plan the analytical activities in an effective manner based on the given timeline to facilitate progress of the projects.
8. Allocation of daily work based on priorities.
9. To guide team members for develop effective analytical methods for developmental projects.
10. To have effective coordination between all concerned functions to facilitate timely completion of projects.
11. Literature Search for development of analytical methods.
12. Review of analytical data generated in the laboratory.
13. Prepare analytical method transfer protocol and reports.
14. Review of calibration reports.
15. Preparation and updation of STP and analytical related SOPs.
16. Laboratory resources management.
Desired Candidate Profile
- Sound knowledge of Chemistry and analytical method development, Instrumental method of analysis and logical approach.
- Hands on experience on Instruments viz., GC, HPLC, Ion Chromatography, UV and Dissolutions apparatus etc.
- Knowledge of regulatory requirements for different markets (US, EU, Canada etc.)
- Knowledge on ICH guidelines, forced degradation studies, impurity profile etc
Time and Venue
21st December , 10.00 AM – 4.00 PM
Venue: Watson Pharma Pvt Ltd (A Teva co.) Unit II,Plot No.K7,Additional MIDC, Ambernath East, 421506
Contact – Pranita Padte
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