Job Description
- Perform and review method validation of Assay, Dissolution, Related compound and Residual solvents etc. for new projects using instruments like HPLC,UV, IC ,GC,ICP MS and AAS etc.
- Preparation of method validation/verification protocol (API and finish product) like HPLC, GC, IC, and AAS etc.
- Preparation of STPs and Specifications as per method validation protocol.
- Check the method transfer protocol/report and methods and resolve the query of Assay, Dissolution, Related compound, Elemental analysis and Residual solvents etc.
- To attain and complete self-training record.
- To coordinate with ARD-Development, QA and QC.
- Ensure timely completion of validation/verification and method transfer.
- Check all availability like the column, Impurities, reference standard, chemicals and reagents etc. as per MOA/Protocol for exhibit batches analysis/validation/Verification.
- To keep the workplace neat and clean and follow Good laboratory practice in the laboratory.
Qualifications
M. Pharm / M. Sc.
About Us
Amneal is an equal opportunity employer. We do not discriminate based on caste, religion, gender, disability, or any other legally protected status. We believe in fostering a workplace that values diversity and inclusion.
