Research Scientist - Pharma Formulations

Role Overview:The Research Scientist - Pharma Formulations will be responsible for the research, development, and optimization of pharmaceutical dosage forms in alignment with global quality, regulatory, and compliance standards. The role supports formulation development from early research through scale-up, technology transfer, and commercialization for regulated markets.Key Responsibilities:- Design, develop, and optimize pharmaceutical formulations including oral solid, liquid, semi-solid, and/or parenteral dosage forms. - Conduct pre-formulation studies to evaluate API characteristics, excipient compatibility, and stability profiles. - Develop robust formulation strategies to enhance bioavailability, stability, and manufacturability. - Execute laboratory experiments, analyze data, and document results in compliance with GLP, GMP, and ICH guidelines. - Perform scale-up studies and support technology transfer to pilot and commercial manufacturing sites. - Prepare and review development reports, protocols, and scientific documentation for internal and regulatory submissions. - Support regulatory filings including ANDA, NDA, CTD, and DMF documentation as applicable. - Collaborate cross-functionally with Analytical R&D, Quality, Regulatory Affairs, Manufacturing, and Project Management teams. - Investigate formulation issues, conduct root-cause analysis, and implement corrective and preventive actions. - Stay updated with advancements in formulation science, novel drug delivery systems, and industry best practices. - Ensure compliance with data integrity, EHS, and company quality systems.Required Qualifications & Skills:- Master’s or PhD in Pharmaceutics, Pharmaceutical Sciences, Chemistry, or related discipline. - Proven experience in pharma formulation R&D within a regulated environment or multinational organization. - Strong understanding of excipients, formulation principles, and drug delivery technologies. - Hands-on experience with laboratory equipment and formulation development techniques. - Knowledge of ICH, USFDA, EMA, and global regulatory requirements. - Strong analytical, problem-solving, and documentation skills. - Ability to work independently as well as in cross-functional, global teams. - Experience with complex formulations such as modified release, injectables, or novel drug delivery systems. - Exposure to global regulatory submissions and audits.

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