Medreich R&D, a Meiji Group Company, is inviting applications for its Regulatory Affairs (RA) Team in Bengaluru (Bommasandra). This is a golden opportunity for M.Pharm graduates (Pharmaceutics only) with 1–3 years of experience in Regulatory Affairs formulation background. If you have expertise in dossier compilation, technical document review, and deficiency management for regulated markets, this role could be the perfect next step in your pharma career.
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Key Responsibilities
As part of the Regulatory Affairs team, you will:
- Conduct technical review and compilation of registration dossiers for regulated markets.
- Review master documents including Specifications, MFR, BMR, BPR, PVP, PVR, HTSP, HTSR, PDR, elemental impurity risk assessments, nitrosamine risk assessments, and stability protocols.
- Handle DMF submissions and updates.
- Manage deficiencies and queries from regulatory authorities for filed products.
Required Qualifications
- Education: M.Pharm (Pharmaceutics only).
- Experience: 1–3 years in core Regulatory Affairs – formulation background.
- Location: Bengaluru (Bommasandra).
- Availability: Candidates who can join within 30 days.
- Note: Freshers are not eligible.
Why Join Medreich R&D?
- Be part of a Meiji Group Company with a strong global presence.
- Gain exposure to regulated market submissions and complex RA documentation.
- Collaborative and growth-oriented work culture.
How to Apply
Interested and eligible candidates can send their resume directly to:
📩 vineeta.k@medreich.com
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