Company Description Bliss GVS Pharma Ltd. is a fast-growing pharmaceutical company focused on developing, manufacturing, and marketing high-quality, affordable formulations for global markets. The organization is a world leader in suppositories and pessaries, offering one of the largest product portfolios in these dosage forms across multiple therapeutic categories. Its manufacturing plants are certified cGMP compliant and meet EU GMP, WHO GMP, OHSAS-18001:2007, and ISO-14001:2004 standards, making it the only EU-GMP certified suppository manufacturer in India.

Bliss GVS also holds segment leadership in anti-malarial products across many African markets, with a broad range of Artemisinin-based combination therapies. With expanding R&D;, manufacturing, and marketing capabilities across more than sixty countries, the company is positioned for strong future growth and innovation.

Role Description The Executive Research and Development Documentation role is a full time, on-site position based in Mumbai. The role involves preparing, reviewing, and maintaining R&D; documentation, including study protocols, technical reports, validation documents, and product development records in alignment with regulatory and internal quality standards. The executive will collaborate with formulation, analytical, and quality assurance teams to ensure accurate data capture, version control, and timely submission of documentation for internal approvals and regulatory filings.





Day-to-day responsibilities include coordinating information from cross-functional stakeholders, ensuring documentation complies with cGMP and global regulatory expectations, and supporting audits by organizing and presenting R&D; records. The role also involves continuous improvement of documentation practices, templates, and workflows to enhance efficiency, traceability, and compliance.

Qualifications

- Strong skills in scientific and technical writing, document formatting, and preparation of R&D; reports, protocols, and summaries.
- Experience with documentation control, data organization, version management, and archiving within pharmaceutical or related industries.
- Familiarity with cGMP, EU GMP, WHO GMP, and regulatory documentation requirements for pharmaceutical development and validation.
- Proficiency in using office productivity tools (such as word processing, spreadsheets, and document management systems).
- Bachelor’s or Master’s degree in Pharmacy, Pharmaceutical Sciences, Chemistry, or a related scientific discipline.
- Attention to detail, strong analytical and problem-solving abilities, and a structured approach to managing multiple projects and deadlines.
- Effective written and verbal communication skills, with the ability to collaborate across R&D;, QA, regulatory, and manufacturing teams.
- Prior experience in R&D; documentation or pharmaceutical regulatory affairs is an advantage; exposure to suppositories, pessaries, or anti-malarial products is beneficial.

📌 Executive Research And Development Documentation (Mumbai)
🏢 Bliss GVS Pharma
📍 Mumbai