Azelis
Freshers
Azelis
Freshers
Lilly
2–4 years of scientific/regulatory writing
Evolet Healthcare
2–6 years
Novumgen
Freshers - 3 Years
Novumgen
0–1 Year
GlobalData
1–2 Years in drug development, clinical trials, regulatory affairs, and pharmaceutical market intelligence
Maven Profcon Services LLP
1–2 Years
Parexel
2 to 4 years
Hindustan Laboratories
1–10 Years
Sandoz
3 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.