## Job highlights
- Support technology transfer,exhibit batch analysis,and regulatory submissions
- 28 years of experience in Analytical RD,preferably in Oncology formulations or APIs
- Qualifications

Experience:
. MSc / MPharm/BPharm / Chemistry or related discipline

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.
- Solid 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.

📌 Trainee Research Associate (Hyderabad)
🏢 Hetero
📍 Hyderabad