Medopharm Hiring Regulatory Affairs Department

- Medopharm is Hiring: Regulatory Affairs Professionals (Experienced)
- About Medopharm
- Key Job Highlights
- Department: Regulatory Affairs
- Location: Tamil Nadu
- Experience: Minimum 5+ Years
- Responsibilities:
- Required Qualifications:
- Why Choose Medopharm?
- How to Apply:
- Relevant Courses for This Role:
- High CPC SEO Keywords Used:
- Two-Column Summary Table
Regulatory Affairs Openings for B.Pharm/M.Pharm Graduates – 5+ Years Experience Required – Apply Now
Medopharm is hiring Regulatory Affairs professionals with B.Pharm/M.Pharm and 5+ years experience at its headquarters. Apply now for a rewarding career in Regulatory Affairs. Location: Tamil Nadu
Medopharm is Hiring: Regulatory Affairs Professionals (Experienced)
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📱 Join Click HereIf you have experience in Regulatory Affairs and are looking for a challenging role in a well-established pharmaceutical company, this opportunity is tailored for you. Medopharm is currently inviting applications for its Regulatory Affairs department at its corporate office in Tamil Nadu.
This opening is ideal for candidates with a background in B.Pharm, M.Pharm, or equivalent life science qualifications who possess deep experience in regulatory dossier preparation and BE studies support.
About Medopharm
Medopharm is one of India’s most respected pharmaceutical companies, with a global presence in more than 100 countries. Known for its high standards of quality and compliance, Medopharm focuses on generic drug development and exports to regulated markets.
Key Job Highlights
Department: Regulatory Affairs
Location: Tamil Nadu
Experience: Minimum 5+ Years
Responsibilities:
- Dossier preparation and lifecycle management for regulated markets
- BE study support for WHO PQ submissions and EU regulations
- Handling queries raised by regulatory authorities
- Liaison with internal R&D and external regulatory bodies
Required Qualifications:
- B.Pharm, M.Pharm or M.Sc in Regulatory Science/Life Sciences
- Minimum 5 years of experience in a Regulatory Affairs role in a pharma company
- Proven record of submitting dossiers to European authorities and WHO PQ
- Excellent understanding of BE (Bioequivalence) studies
Why Choose Medopharm?
- Exposure to global regulatory markets
- Career growth with industry leaders
- Work-life balance with a professional environment
How to Apply:
Qualified professionals can send their CVs directly to hr@medopharm.com.
Note: Only shortlisted candidates will be contacted.
Relevant Courses for This Role:
- Bachelor of Pharmacy (B.Pharm)
- Master of Pharmacy (M.Pharm)
- M.Sc. in Regulatory Affairs or Life Sciences
- Postgraduate Diploma in Regulatory Affairs
High CPC SEO Keywords Used:
- Regulatory Affairs Pharma Jobs
- B.Pharm Jobs India
- M.Pharm Regulatory Affairs Jobs
- Dossier Preparation Jobs
- WHO PQ Regulatory Role
- European Market Pharma Openings
- BE Study Support Career
Two-Column Summary Table
Category | Details |
---|---|
Company Name | Medopharm |
Current Vacancies | Regulatory Affairs Department |
Required Education | B.Pharm, M.Pharm, M.Sc. in Life Sciences |
Experience Required | Minimum 5+ years |

To apply for this job please visit medopharm.com..