Medreich is a pharmaceutical company that has been in existence since 1976, manufacturing generic and branded drugs in several therapeutic areas. With more than 2900 employee€™s worldwide, exceptional quality standards and a client base that is spread across 54 countries, Medreich has built a reputation for raising the bar on product superiority with every undertaking. Medreich’s Research & Development and manufacturing facilities have received the seal of approval from leading global regulatory bodies such as -UK MHRA, Australia TGA, SA MCC, Health Canada, French FDA. The company produces drugs for leading, global pharmaceutical companies such as GSK, Pfizer, Sanofi Aventis, Wyeth, Merck, among others. Medreich has 8 manufacturing facilities built to comply International regulatory standards. Two newly added facilities are State of the art technology driven plants. One among them has the capacity to produce 9 billon tablets and capsules per annum.
Openings for Regulatory Affairs @ Medreich Limited
- Total Vacancies: 3
- Experience: 3-8 years
- Position:
- 1. Executive
- 2. Officer
- 3. Asst. Manager
- Qualification: Must – Educational qualification: M.Pharm/B pharma/Msc
- The desired Qualification is M Pharma.
- The position is based at our Bengaluru Corporate Office.
Also Read: Bafna Pharmaceuticals – Urgent Openings for Production / Packing / Quality Control
Roles and Responsibilities:
1. Candidate should have prior registration experience in EU/UK. – ASIAN/CIS/ROW
2. Should be able to handle projects (initial submission/query response/post-approval) independently.
3. Dossier filing and Variation filing
4. Should have very good communication skills
5. Well-versed with relevant guidelines including ICH.
Interested may kindly share the profiles
rajesh.v@medreich.com / aravinda.p@medreich.com
Also Read: HETERO – Immediate Openings for FRESHERS in AR&D Department @ BADDI
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