JobRaahGet matched free

Jobs

Research Lead

Zimlab · Kalameshwar · India · On-site

Pay: INR 350,000 – 450,000 a year

Posted Jul 30, 2026

Apply with JobRaah

Sign up free: we match you to jobs like this, tailor your application and fill the form. 2 free applications every day.

Job Description: Research Lead – R&D Formulation Development (Pharma) Job Title: Research Lead – R&D Formulation Development Location: Kalmeshwar, Maharashtra Industry: Pharmaceutical Manufacturing Experience: 2–5 Years Education: M.Pharm (Pharmaceutics / Pharmaceutical Technology / Industrial Pharmacy) Key Responsibilities Develop and optimize oral solid, liquid, semi-solid, or other dosage forms. Conduct pre-formulation studies and compatibility evaluations. Design and execute laboratory experiments for formulation development. Prepare prototype, pilot, exhibit, and validation batches. Perform process optimization and scale-up activities. Conduct stability studies and analyze stability data. Prepare development reports, batch records, product development reports (PDR), and regulatory documentation. Support technology transfer from R&D to manufacturing. Coordinate with Analytical R&D, Quality Assurance, Production, Regulatory Affairs, and Packaging teams. research lead R&D formulation development 2-5 YEARS Kalmeshwar M.Pharma education job description pharma industry ChatGPT said: Job Description: Research Lead – R&D Formulation Development (Pharma) Job Title: Research Lead – R&D Formulation Development Location: Kalmeshwar, Maharashtra Industry: Pharmaceutical Manufacturing Experience: 2–5 Years Education: M.Pharm (Pharmaceutics / Pharmaceutical Technology / Industrial Pharmacy) Job Summary We are seeking a motivated Research Lead – Formulation Development to support the development of pharmaceutical formulations from laboratory scale through technology transfer. The candidate will participate in formulation design, optimization, documentation, stability studies, and cross-functional collaboration while ensuring compliance with regulatory and quality standards. Typical responsibilities for professionals with 2–5 years of experience include formulation development, process optimization, documentation, and technology transfer activities. P PharmaGend+1 Key Responsibilities Develop and optimize oral solid, liquid, semi-solid, or other dosage forms. Conduct pre-formulation studies and compatibility evaluations. Design and execute laboratory experiments for formulation development. Prepare prototype, pilot, exhibit, and validation batches. Perform process optimization and scale-up activities. Conduct stability studies and analyze stability data. Prepare development reports, batch records, product development reports (PDR), and regulatory documentation. Support technology transfer from R&D to manufacturing. Coordinate with Analytical R&D, Quality Assurance, Production, Regulatory Affairs, and Packaging teams. Ensure compliance with GMP, GLP, ICH guidelines, SOPs, and data integrity requirements. Troubleshoot formulation and manufacturing issues using scientific approaches. Required Qualifications M.Pharm in Pharmaceutics, Pharmaceutical Technology, Industrial Pharmacy,…