NDDS - (Injectable) Formulation & Development

Intas; Ahmedabad District; On-site; INR 800,000 - 1,500,000; Full time

Job summary

Intas is seeking a qualified formulations expert to develop injectable dosage forms including lyophilized injections, liquids, and pre-filled syringes. The role involves planning formulation trials, scale-up, and lifecycle management across development and transfer to manufacturing sites.

The candidate should have postgraduate degrees in pharmaceutics and hands-on experience in stability studies, particle size, and viscosity analysis within regulated environments.

Qualifications

• Postgraduate degree in pharmaceutics is required or preferred.
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Responsibilities

• Develop injectable dosage forms including lyophilized injections and PFS.
• Coordinate formulation trials and lifecycle management projects.
• Scale-up formulations from lab to pilot and exhibit batches.
• Support technology transfer to manufacturing sites.
• Prepare and review protocols, reports, and stability protocols.

Skills

Formulation development

Pre-formulation studies

Process optimization

Technology transfer

Stability testing

Analytical characterization

Education

M.Pharm (Pharmaceutics)

M.S. (Pharmaceutics)

M.Tech (Pharmaceutical Technology)

Tools

Particle size analysis

Zeta potential analysis

Reconstitution studies

Viscosity measurements

Job description

Role & responsibilities

• Develop injectable dosage forms including:
• Lyophilized injections
• Liquid injections
• Pre-filled syringes (PFS)
• Depot formulations
• Liposomes, microspheres, nanoparticles, and other NDDS-based products
• Conduct pre-formulation studies and compatibility assessments.
• Design and execute formulation trials for new products and lifecycle management projects.
• Optimize formulation composition and manufacturing processes.
• Develop and optimize manufacturing processes for injectable products.
• Scale-up formulations from laboratory to pilot and exhibit batches.
• Support technology transfer to manufacturing sites.
• Investigate formulation and process-related challenges during development and scale-up.
• Coordinate characterization studies including:
• Particle size analysis
• Zeta potential
• Reconstitution studies
• Viscosity measurements
• Stability evaluations
• Prepare and review:
• Protocols and reports
• Development reports
• Technology transfer documents
• Risk assessments
• Stability protocols
• Support dossier preparation for regulated markets such as USFDA, EMA, MHRA, TGA, etc.
• Maintain data integrity and compliance with ALCOA+ principles.

Educational Qualification

• M. Pharm (Pharmaceutics)
• M.S. (Pharmaceutics)
• M. Tech (Pharmaceutical Technology)