Work as QC, QA, Production, Method devlopment, Technical & Scientific in Teva Pharmaceutical | Only experience Candidate
Established In 1901, Teva Pharmaceutical Industries Limited is rated among ten top Pharmaceutical Companies in the World Headquartered in Israel. Teva is active in 60 countries, with over 45.000 dedicated employees worldwide.
Tevapharm India Private Limited, an affiliate of Teva in India has Manufacturing facility (EOU) for Tablets & Capsules & a Laboratory Hub providing Analytical Development, Method Development & Stability Control services globally .located at Verna Goa The Lab Hub is capable of handling OSD's, semisolids & other dosage forms & Is equipped with state-of-the-art machinenes. lab instruments like ULPC. LCMSetc.
We are on the lookout for talented, self reliant & growth oriented professionals from reputed Pharmaceutical Formulation Units at various levels for our expanding business needs at Goa in the following functions.
Post: QC, QA, Production, Method devlopment, Technical & Scientific
QUALITY CONTROL / STABILITY CONTROL
Graduates / Post Graduates in Pharmacy or Chemistry with experience ranging from 2- 6years handling Lab Instruments like HPLC / Dissolution instalments
M.Pharm / B.Pharm / M.Sc (Chemistry) with experience ranging from 2- 5 years with exposure to Method Development & Validation areas.
M.Pharm / B.Pharm with experience ranging from 5- 8 years in IPQA and other Quality Systems.
TECHNICAL AND SCIENTIFIC AFFAIRS
M.Pharm / B.Pharm with experience ranging from 5- 8 years in Technology ' Transfer related activities.
M.Pharm / B.Pharm with experience ranging from 3- 6 years in manufacturing, packing of oral solid dosage forms having worked in granulation, compression . coating, primary and secondary packaging operations.
Interested candidates can send / email their resumes to:
The Director - Human Resources
Tevapharm India Private Limited
Plot No.A-1. Phase I-A. Verna Industrial Estate
Verna - GOA 403722
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