Research Associate

4 days ago


Telangana, India Piramal Pharma Solutions Full time

Business: PPL Digwal
- Department: PTS
- Location: Digwal
- Job Overview: To perform AR&D actives as per GMP & Safety
- Travel Requirements: NA
- Reporting Structure:

- Reports to Research Scientist - AR&D (Service)
- Key Stakeholders:

- Internal: QC, QA, SCM & Safety
- External: NA
- Experience:

- 4-8 Year Experience in manufacturing (API) as per Pharma Manufacturing GMP requirements.- Key Roles & Responsibilities
- 1. Capable to handle independent projects
- 2. Analytical testing support to PDG synthetic group.
- 3. Coordinate with QA regarding method transfer, CCF and investigation reports.
- 4. Experience of handling of HPLC, GC, Potentiometer, Polarimeter instruments.
- 5. API Stability knowledge.
- 6. Capable to handle analytical method development, Implementation, Validation as per requirement.
- 7. Should have experience of Analytical method transfer to QC.
- 8. Experience of making documents like method transfer protocol & report, method validation protocol & report, method development report, specification, standard test procedure etc.
- 9. Should aware about GLP practices and 21 CFR part-11.
- 10. Keep the work area clean and the laboratory under controlled temperature.
- 11. Calibrate the instruments according to the master calibration schedule and follow GLP and SOPs.
- 12. Understand the safety and environmental aspect.
- 13. Maintain the reagents and standardize the volumetric solutions as per schedule.
- 14. Maintain the laboratory journals and instrument log books online.
- 15. Ensure compliance to Hazardous waste and chemical management.



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