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Mepro Pharmaceuticals Hiring in Multiple Departments

Mepro Pharmaceuticals Hiring in Multiple Departments

Mepro Pharmaceuticals is hiring experienced professionals for QA, QC, Regulatory Affairs, Warehouse & Production roles in Vadodara. Apply now for pharma careers with 1–12 years of experience.

Mepro Pharmaceuticals is Hiring Across Multiple Departments in Vadodara – August 2025

Mepro Pharmaceuticals, a reputed name in the pharmaceutical manufacturing sector, is inviting applications from skilled professionals for various positions across Quality Control (QC), Quality Assurance (QA), Regulatory Affairs (RA), Warehouse, and Production. With opportunities for candidates from 1 to 12 years of experience, this recruitment drive is a great chance to join a leading organization known for its compliance, innovation, and global market presence.

Current Openings & Requirements

📍 Location: Vadodara, Gujarat
💼 Experience Range: 1 to 12 Years
🎓 Qualification: B.Sc, M.Sc, B.Pharm, M.Pharm

Quality Assurance (QA – OSD & Injectable)

  • Assistant Manager (10–12 Years) – Lead QMS implementation, manage deviations, CAPA, change control, internal audits, and ensure regulatory compliance.
  • Officer/Sr. Officer/Sr. Executive (2–10 Years) – Handle IPQA, equipment qualification, process validation (PV), and cleaning validation.

Quality Control (QC)

  • Sr. Executive (8–10 Years) – Review and approve QMS documents ensuring GDP & GLP adherence.
  • Officer (2–5 Years) – Perform Raw Material (RM) and Finished Product (FP) analysis for Injectable lines.
  • Officer/Sr. Officer – Microbiology (1–2 Years) – Conduct environmental monitoring, water sampling, and aseptic area testing.

Regulatory Affairs (RA)

  • Officer/Sr. Officer/Executive (2–5 Years) – Review CMC documents, prepare CTD & ACTD format dossiers, and handle regulatory submissions.

Warehouse

  • Officer/Sr. Officer/Executive (2–7 Years) – Manage raw materials, packaging materials, finished goods, inventory, and dispensing.

Production – OSD

  • Officer (2–4 Years) – Oversee capsule manufacturing in the Oral Solid Dosage section, ensuring GMP compliance.

Why Join Mepro Pharmaceuticals?

  • Work with a company recognized for USFDA, EU-GMP, and WHO compliance.
  • Opportunities for growth across OSD & Injectable manufacturing units.
  • Exposure to international regulatory standards.

Application Process

Qualified candidates are encouraged to email their updated CVs to:
📧 hr3@mepro.in

This recruitment is a prime opportunity for pharma professionals to advance their careers in Vadodara’s thriving pharmaceutical hub with Mepro Pharmaceuticals, a company committed to quality, compliance, and innovation.

Written by Pasupuleti

Empowering Aspirations: Your Ultimate Guide to Career and Academic Excellence.

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