Research Scientist - Tech Transfer

DIFGEN PHARMACEUTICALS PRIVATE LIMITED; Hyderabad; On-site; INR 600,000 - 800,000; Full time

Job summary

DIFGEN PHARMACEUTICALS PRIVATE LIMITED is seeking a skilled professional to assist in the execution of formulation and process technology transfers from R&D to manufacturing in Hyderabad. The ideal candidate will have a B.Pharm or M.Pharm in Pharmaceutics and 2-5 years of relevant experience.

Responsibilities include preparation of Batch Manufacturing Records, coordination across various teams, and ensuring compliance with GMP standards. Strong communication and teamwork skills are essential.

Qualifications

• 2-5 years of experience in formulation development, MS&T, or technology transfer.
• Exposure to solid orals, liquids, or softgel capsule dosage forms.
• Understanding of scale-up principles and validation practices.

Responsibilities

• Assist in formulation and process tech transfers from R&D to manufacturing.
• Support the preparation and review of Batch Manufacturing Records (BMRs).
• Coordinate across teams for effective knowledge transfer.

Skills

Formulation development

Process technology transfer

Good communication

Documenting technical reports

Teamwork skills

Education

B.Pharm / M.Pharm in Pharmaceutics or Pharmaceutical Technology

Job description

Job Details

Job Location: DifGen Pharmaceuticals Pvt Ltd- R&D - Prashanti Nagar IE Kukatpally Hyderabad, TELANGANA 500072

Job Shift: Day

Responsibilities

• Assist in the execution of formulation and process technology transfers from R&D to manufacturing sites (in-house and CMO).
• Conduct scale-up and exhibit batches under supervision, ensuring proper documentation and parameter tracking.
• Support in the preparation and review of Batch Manufacturing Records (BMRs) and validation protocols/reports.
• Coordinate with R&D, QA, QC, Regulatory Affairs, and Manufacturing teams for effective knowledge transfer and execution.
• Participate in process investigations, troubleshooting, and deviation handling during trial and validation batches.
• Assist in equipment selection and capacity assessment based on product-specific requirements.
• Ensure document readiness for regulatory submissions, respond to technical queries, and support audit preparation.
• Support internal and external/vendor audits by providing required documentation and technical inputs.
• Contribute to continuous improvement initiatives and support knowledge‑sharing activities within the MSTG team.
• Prepare data summaries, technical reports, and presentations as per project or management requirements.
• Maintain accurate records, follow applicable SOPs, and ensure strict GMP compliance in all operations.

Qualifications & Skills

• B.Pharm / M.Pharm in Pharmaceutics or Pharmaceutical Technology.
• 2–5 years of experience in formulation development, MS&T, or technology transfer.
• Exposure to solid orals, liquids, or softgel capsule dosage forms.
• Understanding of scale-up principles, equipment functionality, and validation practices.
• Familiar with regulatory expectations (USFDA, EU, etc.) and cGMP standards.
• Good communication, documentation, and teamwork skills.
• Willingness to travel to manufacturing sites as per project requirements.