Research Scientist

To perform calibration of the analytical instruments as per calibration schedule and follow the standard practices c-GLP during lab experiments. You will be responsible for cleaning verification method development and validation, API method evaluation and verification, as well as API solubility study assessment. Additionally, you will be involved in working standard qualification, method development for drug product formulation, routine analysis of development samples and lab stability samples, and method verification of different analytical methods. Your role will also include reporting of analytical data and submitting it for review and release, developmental release of raw material and packaging material, and preparation of test procedures for routine development analysis. You will be expected to follow in-house compliance systems, maintain hygienic conditions in the respective department, ensure the use of personal protective equipment, attend EHS training, and manage waste disposal according to EHS requirements. Effective communication is key as you will be required to liaise with formulators for analysis and data submission, CRA for project-specific technical documents/queries, suppliers/vendors for instrument maintenance and inquiries about columns/chemicals, and outside analytical labs for specific analysis. Following GxP (GMP, GDP, GLP) for all processes is essential in this role. Qualifications: - M. Pharmacy/M.Sc/Ph.D Required Skills: - Method development - Data review About Us: In the three decades of its existence, Piramal Group has pursued a twin strategy of both organic and inorganic growth. Driven by its core values, Piramal Group steadfastly pursues inclusive growth while adhering to ethical and values-driven practices. We base our employment decisions on merit considering qualifications, skills, performance, and achievements, ensuring equal opportunities for all applicants and employees in personnel matters. About The Team: Piramal Pharma Solutions (PPS) is a Contract Development and Manufacturing Organization (CDMO) that offers end-to-end development and manufacturing solutions across the drug lifecycle. Through a globally integrated network of facilities in North America, Europe, and Asia, we provide a comprehensive range of services including drug discovery solutions, process & pharmaceutical development services, clinical trial supplies, commercial supply of APIs, and finished dosage forms. Job Identification: 7889 Job Category: Analytical Development Posting Date: 03/14/2025, 04:17 AM Degree Level: Master's Degree Job Schedule: Full time Location: Plot No:-19, PHARMEZ, Sarkhej-Bawala NH-8A, Ahmedabad, Gujarat, 362001, IN,