Hiring for Regulatory Affairs Professionals at Mepro Pharmaceuticals Pvt. Ltd. (Unit-III, Vadodara)-Apply before 25th June 2025

About Mepro Pharmaceuticals

Mepro Pharmaceuticals Pvt. Ltd., with over five decades of pharmaceutical manufacturing expertise, is a leading name in the production of tablets, capsules, creams/ointments, and sterile injectables.
With regulatory approvals from UK-MHRA, EU-GMP, and PIC/S nations, Mepro has established a strong global footprint.

---

Current Openings – Regulatory Affairs Department

We are looking for skilled, experienced, and motivated professionals to join our Regulatory Affairs team at Unit-III, Vadodara, Gujarat.

---

🔹 Assistant / Deputy Manager – Injectable Products

• Experience: 10 to 16 years

• Qualification: B.Pharm / M.Pharm

• Responsibilities:

  • Review & submission of injectable dossiers (CTD/ACTD) for TGA and Europe

  • Handle ICH-compliant lifecycle management

  • Address global regulatory queries and ensure documentation compliance

---

🔹 Assistant / Deputy Manager – OSD Products

• Experience: 10 to 16 years

• Qualification: B.Pharm / M.Pharm

• Responsibilities:

  • Responsible for country-specific submissions in CTD/ACTD format

  • Lifecycle management & global compliance for OSD products

  • Coordinate responses to health authority queries

---

🔹 Officer / Sr. Officer / Executive – Injectable Dossier Preparation

• Experience: Up to 5 years

• Qualification: B.Pharm / M.Pharm

• Responsibilities:

  • Prepare and submit injectable product dossiers (CTD)

  • Coordinate with cross-functional teams for technical documentation

  • Track compliance for new injectable developments and review CMC

---

🔹 Officer / Sr. Officer / Executive – OSD Dossier Preparation

• Experience: 1 to 4 years

• Qualification: B.Pharm / M.Pharm

• Responsibilities:

  • Prepare CTD/ACTD/country-specific dossiers for OSDs

  • Support global tender documentation and ICH-compliant submissions

  • Assist in regulatory lifecycle management activities

---

🔹 Officer / Sr. Officer / Executive – Site Transfer Dossiers (OSD)

• Experience: 1 to 4 years

• Qualification: B.Pharm / M.Pharm

• Responsibilities:

  • Prepare site transfer dossiers and review technical documents

  • Support method validation and document tracking

  • Ensure regulatory alignment and compliance

---

📧 Application Process

Interested candidates may send their updated CV to:
📩 hr3@mepro.in
📝 Subject Code: RA9062025
🗓️ Last Date to Apply: 25th June 2025

---

Join Mepro Pharmaceuticals – Advance Your Career in Global Regulatory Affairs!
Shape the future of safe and compliant healthcare solutions.