Mepro Pharmaceuticals Pvt. Ltd. – Unit-III, a state-of-the-art EU-GMP, MHRA, and WHO-Geneva approved manufacturing facility located in Vadodara, Gujarat, has announced multiple openings in Quality Control, Quality Assurance, and Regulatory Affairs departments for 2025. If you are a passionate pharma professional looking for rewarding pharmaceutical jobs in Vadodara with excellent growth opportunities, this is your chance to join one of India’s leading export-oriented units.
Why Join Mepro Pharmaceuticals Unit-III?
- Work in a fully compliant EU-GMP and MHRA-approved facility
- Exposure to international regulatory standards and global markets
- Strong focus on learning, training, and career progression
- Competitive salary and benefits in the pharmaceutical industry
Available Positions
- Quality Control (QC) – Officer / Executive
- Quality Assurance (QA) – Officer / Executive / Manager
- Regulatory Affairs (RA) – Officer / Executive
Key Responsibilities
Quality Control
- Perform analysis of raw materials, in-process, finished products, and stability samples
- Operate instruments like HPLC, GC, UV, FTIR, etc.
- Prepare and review analytical reports and SOPs
- Ensure compliance with GMP and regulatory guidelines
Quality Assurance
- IPQA, batch release, and documentation review
- Handling deviations, change control, CAPA, and investigations
- Conduct internal audits and vendor qualification
- Validation and qualification activities
Regulatory Affairs
- Preparation and submission of dossiers (CTD/ACTD) for international markets
- Handling post-approval changes and variations
- Liaison with global regulatory agencies
- Keeping updated with EU, MHRA, WHO, and other guidelines
Qualifications & Experience Required
- B.Pharm / M.Pharm / M.Sc (Chemistry / Microbiology)
- 2–10 years of relevant experience in EU-GMP / MHRA-approved plants preferred
- Strong knowledge of current regulatory guidelines
- Excellent communication and documentation skills
Benefits
- Competitive salary package
- Performance-linked incentives
- Medical & accidental insurance
- Subsidized canteen and transport facility
- Continuous training and exposure to global standards
How to Apply
Interested candidates should send their updated CV to: careers@mepro.in Subject Line: Application for [Department] – [Your Name] Example: Application for Quality Control – Rahul Sharma
Applications are accepted immediately. Shortlisted candidates will be contacted for interviews.
Frequently Asked Questions (FAQs)
1. Is prior experience in EU-GMP or MHRA-approved plants mandatory? While preferred, candidates with strong experience in WHO-GMP/USFDA plants and willingness to learn international standards are also encouraged to apply.
2. What is the location of Mepro Pharmaceuticals Unit-III? The facility is located in Vadodara (Baroda), Gujarat.
