Medreich R&D hiring Regulatory Affairs Associate in Bengaluru for M.Pharm graduates with 1–3 years RA experience. Apply now.
About the Company
Medreich R&D, a part of the Meiji Group Company, is a leading pharmaceutical organization with a strong presence in the regulated international markets. The company specializes in research and development, formulations, and providing high-quality pharmaceutical solutions across the globe. With decades of industry expertise, Medreich is known for innovation, regulatory compliance, and commitment to delivering safe, effective medicines.
Joining Medreich means becoming part of a collaborative work environment where employees gain exposure to international regulatory frameworks, formulation development, and dossier management for regulated markets. If you are looking for a career opportunity in Regulatory Affairs (RA), this is your chance to move forward in your professional journey. Regulatory Affairs Job at Medreich RD Hiring
Job Overview
Medreich R&D is inviting applications for the position of Regulatory Affairs Associate for its RA team located in Bommasandra, Bengaluru. This position is ideal for candidates with 1–3 years of experience in Regulatory Affairs (formulation background) who are passionate about dossier compilation, regulatory submissions, and managing technical documentation for global regulated markets. Regulatory Affairs Job at Medreich RD Hiring
Job Details
| Job Title | Regulatory Affairs Associate |
|---|---|
| Company | Medreich R&D (Meiji Group Company) |
| Qualification | M.Pharm (Pharmaceutics only) |
| Experience | 1–3 years in core Regulatory Affairs – formulation |
| Location | Bengaluru (Bommasandra) |
| Joining Requirement | Candidates who can join within 30 days |
| Application Mode | Email Application |
| Freshers Eligibility | Not eligible |
Key Responsibilities
As a Regulatory Affairs Associate at Medreich, you will play a crucial role in regulatory submissions and compliance for regulated markets. Your responsibilities will include: Regulatory Affairs Job at Medreich RD Hiring
- Dossier Compilation and Review
- Preparation and technical review of registration dossiers for regulated markets.
- Ensuring completeness and accuracy of all regulatory submissions.
- Review of Technical Documents
- Reviewing master documents such as:
- Specifications
- Master Formula Record (MFR)
- Batch Manufacturing Record (BMR)
- Batch Packaging Record (BPR)
- Product Validation Protocol (PVP) and Report (PVR)
- Hold Time Study Protocol (HTSP) and Report (HTSR)
- Product Development Report (PDR)
- Elemental Impurity Risk Assessments
- Nitrosamine Risk Assessments
- Stability Protocols
- Reviewing master documents such as:
- Regulatory Submissions
- Handling Drug Master File (DMF) submissions and updates.
- Coordinating with internal teams to ensure timely submissions.
- Deficiency Management
- Responding to deficiencies and queries raised by regulatory authorities.
- Providing clarification and accurate documentation for filed products.
Required Qualifications
- Educational Qualification:
- M.Pharm (Pharmaceutics only).
- Experience:
- 1–3 years in core Regulatory Affairs with formulation background.
- Hands-on experience in dossier preparation, document review, and regulatory submissions for regulated markets.
- Other Requirements:
- Must be able to join within 30 days.
- Strong understanding of regulatory guidelines and documentation.
- Freshers are not eligible for this role.
- Regulatory Affairs Job at Medreich RD Hiring
Why Join Medreich R&D?
Choosing Medreich R&D for your career provides an opportunity to work with a reputed Meiji Group Company that is committed to innovation, regulatory excellence, and professional development. Here are the reasons why this opportunity should not be missed: Regulatory Affairs Job at Medreich RD Hiring
- Global Exposure: Gain experience in regulatory submissions for highly regulated international markets.
- Career Growth: Work on challenging projects that enhance your expertise in Regulatory Affairs.
- Collaborative Environment: Be part of a supportive team that encourages learning and career development.
- Stability and Recognition: Work with an established pharmaceutical company with a strong global presence.
How to Apply
If you meet the eligibility criteria and are interested in this opportunity, you can apply by sending your updated resume to the official recruiter. Regulatory Affairs Job at Medreich RD Hiring
📩 Email ID: vineeta.k@medreich.com
Make sure your subject line clearly mentions:
Application for Regulatory Affairs Associate – Medreich R&D
Application Tips
- Tailor Your Resume: Highlight your Regulatory Affairs experience, dossier preparation skills, and relevant pharmaceutical background.
- Mention Notice Period: Clearly specify your availability to join within 30 days.
- Add a Cover Letter: A short and precise cover letter can make your application stand out.
- Regulatory Affairs Job at Medreich RD Hiring
Final Thoughts
The Regulatory Affairs Associate role at Medreich R&D is a great opportunity for M.Pharm (Pharmaceutics) graduates with relevant experience in RA formulation. With exposure to regulated markets, dossier compilation, technical document review, and deficiency management, this position offers excellent scope for career growth. Regulatory Affairs Job at Medreich RD Hiring
If you are looking to advance your career in the pharmaceutical regulatory domain, Medreich provides the right platform to enhance your skills and gain global experience. Don’t miss this chance to work with a reputed company in the industry.
👉 Apply today and take the next step in your Regulatory Affairs career.
