Research Assocaite / Senior Research Associate - Formulations R&D

Walter Bushnell; Gurugram District; On-site; INR 600,000 - 1,200,000; Full time

Job summary

Walter Bushnell is seeking an experienced Formulation Research & Development (FR&D) professional to drive development, prototype trials, and technology transfer of innovative solid oral and liquid dosage forms.

Role covers literature reviews, development trials, and management of master documents, ERP material/vender code setup, licensing, and QA compliance to support successful product launches.

Qualifications

• 2-5 years of experience in formulation research development.
• MPharma degree from a recognized university.
• Strong knowledge of solid oral dosage form development, including formulation development, prototype development, and scale-up processes.

Responsibilities

• To undertake literature search & preparation of report for a new development project.
• To execute development trials as part of prototype development till technology transfer of new drug products at the manufacturing sites.
• To guide & supervise development trainees or associates during development of new formulations.
• To prepare Master documents of MFC / MFR / BMR / BPR /PVP / Development reports for submission & validation batches.
• Material Master creation of Material code/ Vendor code in ERP.
• MIC creation of Raw material / Packing material / Finished products in ERP.
• Applying Test / Import / Manufacturer Licenses
• Involving all Development QA activities & ensure compliance.

Skills

Formulation development

Prototype development

Scale-up processes

MIC creation

Pharma industry knowledge

Education

M.Pharma

Job description

Walter Bushnell is looking for an experienced Formulation Research & Development (FR&D) professional to drive the development, prototype trial execution, and technology transfer of innovative solid oral / liquid dosage forms.

Role & responsibilities

1. To undertake literature search & preparation of report for a new development project.

2. To execute development trials as part of prototype development till technology transfer of new drug products at the manufacturing sites.

3. To guide & supervise development trainees or associates during development of new formulations.

4. To prepare Master documents of MFC / MFR / BMR / BPR /PVP / Development reports for submission & validation batches.

5. Material Master creation of Material code/ Vendor code in ERP.

6. MIC creation of Raw material / Packing material / Finished products in ERP.

7. Applying Test / Import / Manufacturer Licenses

8. Involving all Development QA activities & ensure compliance.

Desired Candidate Profile

• 2-5 years of experience in formulation research development, preferably in pharmaceutical industry.


• M.Pharma degree from a recognized university.


• Strong knowledge of solid oral dosage form development, including formulation development, prototype development, and scale-up processes.


• Proficiency in creating MIC codes for different product formulations.