Location: Changodar, Ahmedabad

Experience: 0–3 Years

Total Post: 02 No.

Key Responsibilities
Prepare and maintain regulatory documentation.
Develop and review product dossiers.
Create and manage product specifications and STPs.
Prepare and review product labelling and artwork in compliance with regulatory requirements.
Coordinate documentation for regulated and semi-regulated markets.
Ensure compliance with applicable regulatory guidelines and internal quality standards.

Requirements
B. Pharm, M. Pharm, B. Sc, M. Sc
0–3 years of experience in Regulatory Affairs or Documentation.
Positive knowledge of dossier preparation, product specifications, and STPs.
Familiarity with regulatory requirements for regulated and semi-regulated markets is preferred.
Proficiency in Microsoft Word and Excel.
Robust communication, organizational, and documentation skills.
Attention to detail and ability to work independently as well as in a team.





Company Description: SevenQ Nutrition is a full-service third-party nutraceutical manufacturer based in India, supporting D2C brands, pharma companies, wellness startups, and export houses with end-to-end solutions. The company offers a wide range of dosage forms, including gummies, tablets, capsules, syrups, suspensions, soft gels, sachets, and lozenges. SevenQ Nutrition specializes in custom formulation, packaging support, and flexible MOQs to serve diverse business needs. With a robust focus on regulatory compliance, including FSSAI and WHO-GMP standards, the organization is committed to delivering scientifically backed, clean-label health products. Team members join a growing business that values speed, quality, and collaborative product development.

📌 Regulatory Affairs Executive Ahmedabad (India)
🏢 SevenQ Nutrition
📍 India