Develop and optimize analytical methods using techniques such as:
HPLC / UPLC
GC
UV / IR
Dissolution testing
Perform method validation and verification as per ICH and regulatory guidelines.
Conduct method transfer from R&D to QC laboratories.
Analyze samples for assay, impurities, dissolution, and stability studies.
Prepare and review method development reports, protocols, and validation documents.
Troubleshoot analytical issues and improve method robustness.
Maintain laboratory instruments, logs, and calibration records.
Ensure compliance with GLP, GMP, and data integrity requirements.
Collaborate with QA, QC, formulation, and regulatory teams.
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