4 - 7 Years

Job Description

Experience in QC in Formulations regulated manufacturing company. Experience includes analysis of RM/PM/FG, handling HPLC, GC, IR & other sophisticated instruments and document review. Exposure to regulatory audits like USFDA, MHRA is must.

Salary: Not Disclosed by Recruiter

Industry:Pharma / Biotech / Clinical Research

Functional Area:Medical, Healthcare, R&D, Pharmaceuticals, Biotechnology

Role Category:R&D

Role:Analytical Chemistry Associate/Scientist

Employment Type:Permanent Job, Full Time


Desired Candidate Profile

Please refer to the Job description above


UG:B.Sc - Any Specialization

PG:MS/M.Sc(Science) - Any Specialization

Company Profile

Centaur Pharmaceuticals Pvt. Ltd.

Centaur has strategically positioned itself for collaborative partnerships in contract manufacturing and contract research services with its fully scalable 25,000 square metres Oral Solid Dosage (Formulations) Manufacturing and Research facility in Pune.

The facility is inspected and approved by the USFDA, MHRA (UK), TGA Australia, Health Canada, MCC and WHO GMP. Annual capacity of the facility is 3.0 billion tablets and 600 million capsules. It is equipped with high-end machinery for granulations, compression, coating and packaging. Additionally the facility can cater to products that require low RH.
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Recruiter Name:Neelam Bagwe

Contact Company:Centaur Pharmaceuticals Pvt. Ltd.