Job Purpose To perform analytical method development support activities, method validation, method verification, and method transfer for pharmaceutical formulations. The role requires hands-on expertise in chromatographic and analytical instruments, preparation of analytical documentation, data interpretation, and compliance with cGMP, GLP, GDP, and regulatory requirements.

Key Responsibilities
Perform analytical testing for pharmaceutical formulations such as Tablets, Capsules, Gels, and Syrups.
Execute Method Validation, Verification, and Method Transfer activities for Assay, Dissolution, Related Substances, and Residual Solvents.
Prepare Method Validation & Method Transfer Protocols and Reports.
Independently prepare analytical calculation sheets in Excel for Assay, Dissolution, Related Substances, and Residual Solvents.
Operate and maintain analytical instruments including:
Waters HPLC with Empower 3
Dissolution Tester (Auto Sampler)




Gas Chromatography (GC)
UV Spectrophotometer
Karl Fischer Titrator
Potentiometer
Ensure compliance with GLP, GDP, GCP, and Data Integrity requirements.
Maintain accurate analytical documentation and laboratory records.

Required Skills
Hands-on experience with Waters Empower 3 and HPLC systems.
Robust knowledge of Method Validation, Verification, and Transfer.
Sound understanding of pharmaceutical analytical techniques and chromatographic practices.
Proficiency in Microsoft Excel and Word.
Valuable analytical, documentation, and problem-solving skills.

Experience - 5 to 7 Years

Qualification
M.Sc. (Analytical Chemistry / Organic Chemistry) / M.Pharm or equivalent qualification.
Relevant experience in pharmaceutical analytical development.

📌 Research Officer Adl Navi Mumbai (India)
🏢 RPG Life Sciences
📍 India