Formulation Development

Company Description

V. S. International Pvt. Ltd., headquartered in Mumbai, India, is a prominent healthcare company specializing in the manufacture, marketing, and export of pharmaceutical products, medical devices, and healthcare solutions. With operations spanning over 30 countries, the company has been committed to quality, reliability, and innovation since its establishment in 1997. Recognized among the top 100 SMEs by the Ministry of MSME, Government of India, V. S. International has received multiple accolades, including the Indian Exporters’ Excellence Award. Supported by an EUGMP, Health Canada, TGA Australia, and SAHPRA South Africa-accredited manufacturing plant and an in-house R&D facility, the company is a trusted CDMO partner in regulated markets worldwide.

Role Description

This is a full-time, on-site role for a professional in Formulation Development, located in Daman and Diu, India. The role involves developing and optimizing pharmaceutical formulations, conducting experiments, interpreting data, and ensuring regulatory compliance. The professional will collaborate with cross-functional teams, document findings and processes, and contribute to the innovation of new healthcare products through research and development efforts.

Key Responsibility

·      Independently develop IR/ER tablets and Capsule dosage form and track to all development progress.

·      Conduct pre-formulation & excipient compatibility studies (ICH)

·      Design formulation & process using QbD and DoE approach

·      Lead execution of lab/pilot batches and scale-up activities

·    Troubleshoot formulation/process issues using root cause analysis tools

·      Review and prepare documents: PDR, MFC, protocols, reports, regulatory dossiers etc.

·      Collaborate with cross-functional teams: Analytical, QC, QA, RA, Production

·      Ensure cGMP, data integrity and safety compliance throughout development

·      Good knowledge of global regulatory expectations (TGA/CANADA/SAHPRA/EMA/WHO/USFDA/WHO)

. To prepared development report during CFT meeting when required

. Strictly align with company regulatory policies and protocol.

Department : Formulation Development

Experience Required: 5-6 Years