About the role
Key ResponsibilitiesDevelop and validate analytical methods for raw materials, in-process, and finished products.Perform method transfer activities and troubleshoot analytical issues.Prepare analytical protocols, reports, and technical documentation.Ensure compliance with GMP, GLP, and regulatory guidelines.Support stability studies and product development activities.Coordinate with QC, QA, and formulation teams during development and validation stages.Review analytical data and ensure accuracy and integrity of results.Participate in audits and regulatory inspections when required.
Bachelor’s degree in Pharmacy, Chemistry, or related scientific field.4–7 years of experience in R&D Methodology within the pharmaceutical industry.Strong knowledge of analytical instruments such as HPLC, GC, UV, and dissolution apparatus.Good understanding of ICH guidelines and method validation requirements.Good communication and problem-solving skills.
