Biophore India Pharmaceuticals Pvt. Ltd has established itself as a trusted partner for niche and complex products. With 4 US FDA and EU approved API manufacturing facilities, one dedicated intermediate facility and a world class R&D lab housing 400 scientists with varied expertise, Biophore has emerged as one of the leading API companies globally. We have consistently been in the Top 10 US DMF filers with the US FDA over the past 5 years and with most of our APIs, we are one of the fastest companies to bring them to the market enabling wider access for patients worldwide
Greetings from Biophore !!
We are conducting walk in Interviews for AR&D Validation Department !
JD:
1. Having good exposure on Analytical method Validation
2. Instruments Handling like GC, HPLC,LCMS.GCMS
Experience : 2 years to 05 Years
Preferable Only Male Candidates .
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Greetings from Biophore india Pharmaceutical Pvt Ltd
We are hiring for Quality Assurance -API .
Please go through the JD.
- Responsible for Document issuance, Document control and record retention.
- Responsible for review of Analytical Method transfer /Method development reports
- Responsible for review and approval of QMS related documents.(Change control , Incidents , Deviations and OOS )
- Responsible for review and approval of Analytical Method validation documents Like protocal,
- Raw data and reports of HPLC, GC, TLC , Autotitrator, ICP-MS, UV, LCMS, GCMS and PSD instruments .
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Walk In Date :05th May 2023 .
Time :10:00 AM to 03:00 PM
Experience : 2 Years to 9 Years.
Preferable Male Candidates Only
Venue :
Biophore India Pharmaceuticals Pvt. Ltd.
Plot# 231, IDA Phase -II, Pashamylaram,
Biophore Road, Patancheru (M), Hyderabad.
Sangareddy District
Telangana 502307
Documents need to carry :
- 1.Updated CV
- 2.Last 03 Months pay slips
- 3.Copy of educational Documents.
- 4.Latest Increment Letter if you have .
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