Trainee Research Associate
Hetero · Hyderabad · onsite · Posted 1d ago
Undisclosed8–13 yrsfulltimeSourced from
About a minute. You'll make an account on the way through.
About this role
Key Responsibilities:
- Develop and validate analytical methods for oncology drug products and APIs.
- Perform method transfer, method verification, and routine analytical testing.
- Prepare and review analytical protocols, reports, specifications, and stability documents.
- Handle HPLC, UPLC, GC, Dissolution, UV, and other analytical instruments.
- Investigate OOS, OOT, deviations, and laboratory incidents.
- Support technology transfer, exhibit batch analysis, and regulatory submissions.
- Ensure compliance with cGMP, GLP, ICH, USP, EP, and data integrity requirements.
- Maintain accurate documentation and participate in internal and external audits.
Qualifications Experience:
- M.Sc./M.Pharm/B.Pharm/Chemistry or related discipline.
- 28 years of experience in Analytical RD, preferably in Oncology formulations or APIs.
- Strong knowledge of analytical method development, validation, and regulatory guidelines.
Disclaimer: This job posting has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.
Sourced from naukri
Skills
CGMPMethod TransferAnalytical Method DevelopmentResearch Associateapistechnology transferregulatory submissionsauditsChemistryHPLCUPLCAnalytical TestingoncologyResearchcompliance
About Hetero
Hetero
Pharma
3.2k+
employees
1993
33 years old
Hyderabad/Secunderabad, Telangana
India
About
One of the world’s leading producers of key Active Pharmaceutical Ingredients and generic formulations with a presence in 140+ countries and backed by 30 years of experience in the pharma sectors.
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