Are you passionate about advancing healthcare and building a rewarding career in pharmaceuticals? Mepro Pharmaceuticals Pvt. Ltd. (Unit-III), a reputed EU-GMP-approved facility in Vadodara, Gujarat, is hiring talented professionals to join our dynamic team. We’re seeking skilled candidates for roles in Quality Control, Quality Assurance, Regulatory Affairs, Warehouse, and Production (OSD). With competitive salaries, excellent career growth, and a supportive work environment, Mepro offers the perfect opportunity to shape the future of pharma. Apply today and be part of our mission—Committed to Humanity!
Job Responsibilities
Quality Control (Microbiology & Analytical)
- Conduct environment monitoring for injectable areas and aseptic zones.
- Perform water sampling and analysis to ensure compliance with regulatory standards.
- Analyze raw materials (RM) and finished products (FP), adhering to GDP and GLP guidelines.
- Review and approve QMS documents to maintain compliance.
Quality Assurance (OSD & Injectable)
- Execute in-process quality assurance (IPQA) and equipment qualification.
- Conduct process validation (PV) and cleaning validation.
- Implement and maintain QMS, handle deviations, CAPA, change control, and internal audits.
- Ensure regulatory compliance with EU-GMP standards.
Regulatory Affairs
- Review CMC documents for regulatory submissions.
- Compile dossiers in CTD and ACTD formats.
- Ensure accurate documentation for API, finished products, and legal compliance.
Warehouse
- Manage raw materials, packaging materials, and finished goods.
- Oversee material dispensing and inventory management.
- Ensure compliance with Good Distribution Practices (GDP) and regulatory guidelines.
Production (OSD)
- Handle capsule manufacturing activities in the OSD area.
- Ensure compliance with regulatory and EU-GMP standards.
Qualifications
- Quality Control (Microbiology & Analytical): B.Sc/M.Sc with 1-10 years of experience in environment monitoring, water analysis, or QMS document review.
- Quality Assurance (OSD & Injectable): B.Pharma/M.Pharma with 2-12 years of experience in IPQA, process validation, or QMS implementation.
- Regulatory Affairs: B.Pharma/M.Pharma with 2-5 years of experience in CTD/ACTD dossier preparation and CMC document review.
- Warehouse: B.Sc/M.Sc/B.Pharma with 2-7 years of experience in material handling and inventory management.
- Production (OSD): B.Pharma/M.Pharma with 2-4 years of experience in capsule manufacturing.
Benefits
- Competitive Salary: INR 3,00,000–12,00,000 per annum, based on experience and role.
- Career Growth: Opportunities for professional development in an EU-GMP-approved facility.
- Learning Environment: Access to cutting-edge pharma technologies and processes.
- Supportive Culture: Collaborative team environment focused on innovation and humanity.
How to Apply
Interested candidates can send their CV to hr3@mepro.in with the subject line mentioning the department (e.g., “Quality Control Application”). Ensure your CV highlights relevant experience and qualifications. Applications are reviewed on a rolling basis, so apply by September 10, 2025, to be considered.
FAQs
What is the application deadline for these roles?
Applications must be submitted by September 10, 2025, to be considered for the current hiring cycle.
Can I apply for multiple departments at Mepro Pharmaceuticals?
Yes, you can apply for multiple roles by submitting separate applications for each department, clearly mentioning the department in the email subject line.
