About V.S. International Private Limited (VSI)
Established in 1997, VSI is a globally focused pharmaceutical company with a growing presence across Africa, Southeast Asia, the Middle East, and Latin America. Operating across branded generics and contract manufacturing, the company is building a diversified and scalable business model.
Our EU-GMP-approved OSD facility in Daman, with accreditations from leading global regulators, supports an annual capacity of 3 billion tablets and 300 million capsules reflecting our strong manufacturing and compliance backbone.
Driven by a robust R&D pipeline and capabilities in complex formulations and advanced drug delivery systems, VSI is focused on expanding its footprint in regulated and semi-regulated markets while strengthening strategic partnerships globally.
Role & responsibilities
- Sourcing & Supplier Qualification: Identify and qualify suppliers for APIs, excipients, intermediates, reference standards, and specialty reagents; manage supplier questionnaires, audits coordination, and corrective actions.
- Procurement Operations: Raise and manage POs, negotiate lead times and pricing, coordinate expedited shipments for critical experiments, and maintain R&D inventory buffers.
- Regulatory & QA Support: Provide COAs, GMP statements, DMF/CEP references, SDS, and supplier declarations required for regulated markets; support regulatory submissions and audits.
- Technical Ingredient Advisory: Apply knowledge of physicochemical attributes (polymorphs, particle size, hygroscopicity, impurity profiles) to recommend fitforpurpose materials and alternatives.
- CrossFunctional Collaboration: Work closely with formulation, analytical, QA, and regulatory affairs on change controls, supplier changes, and risk assessments.
- Risk & Cost Management: Identify singlesource risks, develop contingency plans, and drive costeffective sourcing without compromising compliance.
- Systems & Documentation: Maintain records in ERP/P2P and supplier management systems; prepare supplier dossiers for audits.
Required Qualifications & Experience
- Education: Bachelors in Pharmacy, Chemistry, Pharmaceutical Sciences, Chemical Engineering, or Supply Chain.
- Technical Knowledge: Strong familiarity with APIs, excipients, reference standards, COA interpretation, and basic analytical method impacts.
Skills & Competencies
- Regulatory awareness: GMP/GDP concepts, DMF/CEP basics.
- Quality orientation: Supplier quality agreements, deviation handling.
- Analytical literacy: Basic understanding of HPLC/GC/Karl Fischer/particle size implications.
- Systems: ERP/P2P, MS Excel; supplier management tools.
- Behavioral: Collaboration, negotiation, attention to detail, problem solving under time pressure.
KPIs & Reporting
- Ontime delivery rate for R&D critical materials.
- Supplier qualification cycle time.
- Timetoresolve supplier quality issues.
- Compliance rate for supplier documentation.
- Reports to: Head of Procurement (R&D) or Procurement Manager.
- Stakeholders: R&D scientists, QA, Regulatory, Manufacturing, Suppliers.