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ZIM LABORATORIES LTD.

Research Lead

Kalameshwar, India

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hirly's read of this role

Seniority
Lead / management
Country
IN
Work mode
On-site / unstated
First seen by hirly
23 Sept 2026

Derived automatically from the posting. Upload your resume above to see how the role scores against it.

the posting

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, or a related specialization.
  • 2–5 years of experience in pharmaceutical Formulation R&D.
  • Hands-on experience in formulation development and process optimization.
  • Knowledge of pharmaceutical excipients, formulation principles, and manufacturing processes.
  • Understanding of regulatory requirements, ICH guidelines, and GMP.
  • Good technical writing and documentation skills.

Preferred Skills

  • Experience with QbD (Quality by Design) and DoE (Design of Experiments).
  • Exposure to technology transfer and scale-up.
  • Knowledge of regulated markets (USFDA, EU, MHRA, WHO-GMP).
Original posting on ZIM LABORATORIES LTD.'s site ↗

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