Bliss GVS Pharma Hiring For Research & Development

Bliss GVS Pharma Ltd. is hiring experienced pharmaceutical professionals for an Executive – R&D Documentation position within its Research & Development department. The opening is based at the company’s Andheri R&D facility in Mumbai and will support both Analytical Research & Development (ARD) and Formulation Research & Development (FRD) documentation activities.

This Bliss GVS Pharma R&D Documentation job is suitable for candidates with an M.Sc in Chemistry or M.Pharm and at least 6 years of relevant R&D documentation experience in a regulated pharmaceutical organization. Candidates with strong knowledge of cGMP, GDP, QMS, pharmacopoeial requirements, SAP, technology transfer documentation and regulatory compliance are encouraged to apply.

Bliss GVS Pharma Job Overview

Key Responsibilities

The selected Executive – R&D Documentation professional will be responsible for managing controlled documentation for the ARD and FRD functions while ensuring compliance with applicable pharmaceutical regulatory and cGMP requirements.

• Prepare, review and update SOPs, specifications, Standard Testing Procedures (STPs), Batch Manufacturing Records (BMRs), Master Formula Records (MFRs), Product Development Reports (PDRs), protocols and reports.
• Prepare and implement product-specific documents including specifications, STPs, MFRs and Technology Transfer documentation.
• Generate, maintain and manage relevant SAP codes for materials and controlled documents.
• Prepare and review documentation associated with change controls, pharmacopoeial updates and Quality Management Systems (QMS).
• Review documentation related to non-conformances, investigations and Corrective and Preventive Actions (CAPA).
• Support preparation of responses to regulatory authority queries, observations and deficiencies.
• Coordinate the timely implementation and availability of approved controlled documents across relevant departments.
• Ensure documentation activities comply with Good Documentation Practices (GDP), cGMP and applicable regulatory requirements.
• Support ARD and FRD teams in maintaining accurate, traceable and inspection-ready pharmaceutical R&D documentation.

Qualification & Experience

Candidates applying for the Bliss GVS Pharma Executive R&D Documentation vacancy should meet the following requirements:

Qualification: M.Sc in Chemistry or M.Pharm.

Experience: Minimum 6 years of R&D Documentation experience within a regulated pharmaceutical company.

Candidates should have practical exposure to pharmaceutical research and development documentation, particularly documentation supporting Analytical R&D (ARD) and Formulation R&D (FRD) operations.

Skills Required

Applicants should possess strong knowledge of:

• Indian Pharmacopoeia (IP), British Pharmacopoeia (BP), European Pharmacopoeia (EP) and United States Pharmacopeia (USP)
• Quality Management Systems (QMS)
• SOP preparation and document control
• Analytical and formulation development processes
• Current Good Manufacturing Practices (cGMP)
• Good Documentation Practices (GDP/cGDP)
• Pharmaceutical regulatory guidelines
• Change control, investigations and CAPA documentation
• Technology Transfer documentation
• MS Word and Microsoft Excel
• SAP systems and document/material code management

Why Consider This Opportunity?

This role provides experienced pharmaceutical R&D professionals an opportunity to work across ARD and FRD documentation activities in a regulated pharmaceutical environment. The position offers exposure to product documentation, technology transfer, QMS, regulatory responses, pharmacopoeial updates and cross-functional R&D operations.

Professionals seeking to strengthen their careers in pharmaceutical R&D documentation, regulatory compliance, document control and quality systems may find the position particularly relevant.

How to Apply for Bliss GVS Pharma R&D Documentation Job

Interested and eligible candidates can send their updated CV/resume to:

Email: hr.careers@blissgvs.com