Employer: Ind Swift Ltd
Industry: Health and Medical, Management
Location: Chandigarh, India

Job Description:

Responsible for International Drug Regulatory Affairs & related documentations & quires, compliance & product life cycle management. Review, submission & approval of registration dossiers for regulated countries, timely regulatory inputs to R&D.

Desired Candidate Profile:

Candidate must be M.Pharma plus diploma in regulatory affairs with 8-10 years of relevant experience in handling international regulatory affair matters into pharma formulation companies. Must have good communication & presentation skills.

Experience: 8 – 12 Years

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