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)
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Develop and optimize oral solid, liquid, semi-solid, or other dosage forms.
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Conduct pre-formulation studies and compatibility evaluations.
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Design and execute laboratory experiments for formulation development.
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Prepare prototype, pilot, exhibit, and validation batches.
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Perform process optimization and scale-up activities.
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Conduct stability studies and analyze stability data.
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Prepare development reports, batch records, product development reports (PDR), and regulatory documentation.
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Support technology transfer from R&D to manufacturing.
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Coordinate with Analytical R&D, Quality Assurance, Production, Regulatory Affairs, and Packaging teams.
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research lead R&D formulation development 2-5 YEARS Kalmeshwar M.Pharma education job description pharma industry
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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)
-
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
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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.
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Ensure compliance with GMP, GLP, ICH guidelines, SOPs, and data integrity requirements.
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Troubleshoot formulation and manufacturing issues using scientific approaches.
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M.Pharm in Pharmaceutics, Pharmaceutical Technology, Industrial Pharmacy, or a related specialization.
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2–5 years of experience in pharmaceutical Formulation R&D.
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Hands-on experience in formulation development and process optimization.
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Knowledge of pharmaceutical excipients, formulation principles, and manufacturing processes.
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Understanding of regulatory requirements, ICH guidelines, and GMP.
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Good technical writing and documentation skills.
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Experience with QbD (Quality by Design) and DoE (Design of Experiments).
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Exposure to technology transfer and scale-up.
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Knowledge of regulated markets (USFDA, EU, MHRA, WHO-GMP).
