Develop and optimize analytical methods using techniques such as HPLC, UPLC, GC, UV, IR, and Dissolution.
Perform method validation and verification as per ICH, GMP, and regulatory guidelines.
Conduct method transfer from R&D to Quality Control laboratories.
Analyze samples for assay, impurities, dissolution, and stability studies.
Prepare and review method development protocols, validation reports, and technical documents.
Troubleshoot analytical issues and improve method robustness and reproducibility.
Maintain laboratory instruments, calibration records, and logbooks.
Ensure compliance with GLP, GMP, and data integrity requirements.
Competitive fixed salary
Performance-based bonus / annual incentive
Overtime or project incentives (in some organizations)
Medical insurance (employee + dependents in many companies)
Accident insurance
Periodic health check-ups
Paid annual / earned leave
Casual and sick leave
Public and festival holidays
Flexible work hours in some R&D environments
Provident Fund (PF) contribution
Gratuity (as per company policy and law)
Long-term savings or retirement plans (company dependent)
Ajanta Pharma's board is supported by several committees, each focusing on specific areas to ensure effective governance: Audit Committee: Oversees financial reporting, internal controls, and audit processes. Stakeholders’ Relationship Commit... Read More