Icon Life Science
0–6 months
Icon Life Science
0–6 months
Accenture
0–1 years
Sun Pharma
0 - 2 Years
Pfizer
0–1 year | 7+ years For Manager
Alcon
1 Years+
Apotex
1 Years+
₹6,00,000–₹10,00,000 per annum
Amgen
Relevant Regulatory/Medical Writing experience
Enovis
Minimum 2 years of medical device industry experience
Indero
0 - 1 Years
Fortrea
2 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.