Abbott
2–5 years of Regulatory Operations or Regulatory Affairs experience
Online Application
Sanofi
2 years of experience in Medical Regulatory Writing or Pharmaceutical Regulatory Writing.
Online Application
Novartis
Minimum 2 Years
Online Application
Johnson & Johnson
4–6+ Years
Online Application
Syneos Health
2–3 years
Email Application
Genedrift
0 - 5 Years
Online Application
ICON
2 years
Online Application
Accenture
0 to 1 years
₹2.8 LPA – ₹4.5 LPA
Online Application
Sandoz
2–4 Years (Analyst), 5–8 Years (Specialist)
Online Application
Accenture
5+ Years
14 - 25 LPA
Online Application
Regulatory Affairs Jobs in India
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
About Regulatory Affairs Jobs
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.
Career Questions
Can freshers enter regulatory affairs?
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.
What is the difference between regulatory affairs and quality assurance?
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.