Process Development Scientist

Role overview

Intas Pharmaceuticals is looking for a Process Development Executive to join the Parenteral Process Development Lab. The position centers on developing robust manufacturing processes for parenteral products, supporting new product launch initiatives, and driving optimization and scale-up work while staying aligned with compliance and quality expectations.

Core responsibilities

• Create, refine, and expand pharmaceutical manufacturing processes for improved performance and scalability.
• Run laboratory trials and assess whether a process can be successfully implemented.
• Assist with moving technology from development into pilot plants and commercial production units.
• Draft, check, and update process development records and reports, including PDRs.
• Work in line with GMP, EHS, and other applicable regulatory standards.
• Support CTD, DMF, and related regulatory documentation and submissions.
• Take part in validation activities, risk evaluations, and process troubleshooting.
• Coordinate closely with Analytical R&D, QA, Production, and Regulatory Affairs teams.
• Offer technical assistance during pilot-scale and commercial-scale batch manufacturing.
• Help with internal and external audits and inspections when needed.

Requirements

• M. Pharm is compulsory for this role.
• Relevant experience of 2 to 8 years in a Process Development Lab for parenteral products within a regulatory-approved pharmaceutical setup.
• Solid grasp of process development fundamentals and scale-up methodology.
• Exposure to new product launch work and campaign-based execution.
• Experience in technology transfer from R&D to manufacturing.
• Working knowledge of regulatory expectations and technical documentation.
• Strong analytical thinking and problem-solving ability.
• Good communication skills and the ability to collaborate effectively in teams.

Additional information

This position is based in Ahmedabad, Gujarat, India and is a full-time, on-site opportunity. The role is focused on parenteral R&D work in a regulated pharmaceutical environment. No stipend, salary, number of openings, start date, or application deadline was specified in the source.