Medtronic
4-7 years
Medtronic
4-7 years
Saviour Pharmaceuticals
0 - 1 Years
Axio Biosolutions
Freshers
18000 Per Month
Hetero
3 – 9 years
Octavius Pharma
1-5 years
₹2.16 - ₹4.8 LPA

Navitas Life Sciences
0 - 5 Years
Thermo Fisher Scientific
2+ years
RegTech India
0-1 year
Achira Labs
2 Years
KLM Laboratories
2 – 12 years
Regulatory affairs professionals help pharmaceutical and healthcare companies prepare, review and maintain submissions, product information and compliance documentation. PharmaBharat lists regulatory opportunities across medicines, medical devices, clinical research and related life-sciences functions.
Related career areas: Quality Assurance · Clinical Research · Medical Writing
Common roles include Regulatory Affairs Associate, Regulatory Submissions Coordinator, CMC Associate, Labelling Specialist and Medical Device Regulatory Executive. B.Pharm, M.Pharm, Pharm.D, chemistry and life-sciences graduates may be eligible depending on the product area and experience level.
Yes. Graduate and trainee roles may be available in submission support, document management, publishing and regulatory operations. Strong technical writing and knowledge of pharmaceutical regulations are useful foundations.
Regulatory affairs focuses on submissions, approvals and communication with health authorities, while quality assurance focuses on systems and processes that maintain product and operational quality.