Job Summary
The F&D Executive is responsible for developing and optimizing pharmaceutical formulations in accordance with regulatory requirements and company quality standards. The role involves conducting formulation trials, preparing development documentation, supporting technology transfer, and coordinating with Production, QA, QC, Regulatory Affairs, and Purchase departments to ensure successful product development and commercialization.
Key Responsibilities
- Develop and optimize formulations for tablets, capsules, powders, liquids, ointments, and other dosage forms.
- Perform laboratory trials and record observations accurately.
- Prepare Master Formula Records (MFR), Batch Manufacturing Records (BMR), and development reports.
- Conduct compatibility, stability, and validation studies.
- Coordinate technology transfer from R&D to commercial manufacturing.
- Monitor pilot batches and troubleshoot formulation-related issues.
- Maintain proper documentation as per GMP, GLP, and company SOPs.
- Prepare and review Standard Operating Procedures (SOPs) related to formulation development.
- Coordinate with QA, QC, Production, Procurement, and Regulatory departments during product development.
- Ensure timely calibration and maintenance of laboratory equipment.
- Participate in investigation of OOS, deviations, change controls, and CAPA related to product development.
- Ensure compliance with WHO-GMP, Schedule M, and applicable regulatory guidelines.
- Maintain laboratory cleanliness and safety practices.
- Assist in new product development and cost optimization initiatives.
- Prepare technical documents for regulatory submissions when required.
Educational Qualification
- M.Pharm (Pharmaceutics / Pharmaceutical Technology) – Preferred
- B.Pharm with relevant experience may also be considered.
Experience
- 2–5 years of experience in Formulation & Development in a pharmaceutical manufacturing company.
- Experience in solid oral dosage forms is preferred.
Required Skills
- Strong knowledge of pharmaceutical formulation development.
- Knowledge of GMP, GLP, WHO-GMP, and Schedule M guidelines.
- Good documentation and report writing skills.
- Familiarity with stability studies and analytical interpretation.
- Proficiency in Microsoft Office (Excel, Word, PowerPoint).
- Good communication and interpersonal skills.
- Strong analytical and problem-solving abilities.
- Ability to work independently and as part of a cross-functional team.
Key Performance Indicators (KPIs)
- Timely completion of formulation development projects.
- Success rate of trial and pilot batches.
- Compliance with GMP and documentation standards.
- Timely technology transfer to production.
- Reduction in formulation-related manufacturing issues.
- Completion of stability studies as per timelines.
- Zero critical documentation errors.
Working Conditions
- Manufacturing and R&D laboratory environment.
- Compliance with PPE, safety procedures, and GMP requirements.
- May require extended working hours during product development, validation, and technology transfer activities.
Pay: ₹20,571.01 - ₹31,044.99 per month
Benefits:
- Flexible schedule
- Food provided
- Health insurance
- Leave encashment
- Paid time off
- Provident Fund
Work Location: In person
