European Regulatory Compliance Expert
2 days ago
Dr. Reddy’s Laboratories is seeking a highly skilled Regulatory Affairs Specialist to oversee the preparation and submission of regulatory dossiers, ensuring compliance and timely approvals.
Job Description:We are looking for an experienced professional to manage activities pertaining to new application submissions for Europe through DCP, MRP, NP. This role will collaborate with European Regulatory authorities and internal teams to ensure regulatory compliance for new applications.
Key Responsibilities:- Preparation, review and submission of new applications through DCP, MRP, NP for EU
- Direct Interaction with EU regulatory authorities
- Handling of deficiencies and timely response to regulatory agencies
- M.Sc or M.pharm qualification
- Minimum work experience: 8 to 12 years of experience in regulatory affairs preferably in Europe registrations
Dr. Reddy’s maintains a work environment, free from discrimination and is an equal opportunity employer. We actively help to catalyse your career growth and professional development through personalised learning programs.
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