Join Mepro Pharmaceuticals Unit-III: Exciting Opportunities in Quality Control, Quality Assurance, and Regulatory Affairs
Summary: Mepro Pharmaceuticals Pvt. Ltd. – Unit-III, a leading export-oriented pharmaceutical manufacturing facility approved by EU-GMP, MHRA, and WHO-Geneva, is seeking talented and passionate professionals to join our dynamic teams in Quality Control, Quality Assurance, and Regulatory Affairs. If you are looking for a rewarding career in a state-of-the-art facility with opportunities for growth and international exposure, we encourage you to apply!
About Mepro Pharmaceuticals Unit-III:
Mepro Pharmaceuticals Unit-III is a modern, fully compliant pharmaceutical manufacturing facility located in Vadodara, Gujarat. We are committed to producing high-quality pharmaceutical products for global markets, adhering to the strictest international regulatory standards. Our facility is approved by EU-GMP, MHRA, and WHO-Geneva, reflecting our dedication to excellence and compliance. We pride ourselves on fostering a culture of learning, innovation, and career advancement for our employees.
Why Choose a Career at Mepro Pharmaceuticals Unit-III?
- Global Standards: Work in a fully compliant EU-GMP and MHRA-approved facility, gaining invaluable experience in international regulatory standards.
- International Exposure: Contribute to the production of pharmaceuticals for global markets and gain exposure to various regulatory requirements.
- Growth Opportunities: We are committed to providing our employees with ample opportunities for learning, training, and career progression.
- Competitive Benefits: We offer a competitive salary and benefits package within the pharmaceutical industry.
- Dynamic Environment: Be part of a team dedicated to excellence and innovation in pharmaceutical manufacturing.
We are currently seeking qualified candidates for the following positions:
- Quality Control (QC) – Officer / Executive
- Quality Assurance (QA) – Officer / Executive / Manager
- Regulatory Affairs (RA) – Officer / Executive
Key Responsibilities:
Quality Control (QC):
- Perform analysis of raw materials, in-process materials, finished products, and stability samples according to established procedures.
- Operate and maintain analytical instruments such as HPLC, GC, UV, FTIR, etc.
- Prepare and review analytical reports, SOPs, and other related documentation.
- Ensure strict adherence to GMP and regulatory guidelines in all QC activities.
- Participate in the investigation of out-of-specification (OOS) results and implement corrective actions.
Quality Assurance (QA):
- Conduct In-Process Quality Assurance (IPQA) checks during manufacturing processes.
- Review batch manufacturing records (BMRs) for completeness and accuracy, and facilitate batch release.
- Handle deviations, change control, CAPA (Corrective and Preventive Action), and investigations related to quality issues.
- Conduct internal audits to ensure compliance with GMP regulations and company policies.
- Perform vendor qualification audits to assess the quality systems of suppliers.
- Participate in validation and qualification activities for equipment, processes, and analytical methods.
Regulatory Affairs (RA):
- Prepare and submit comprehensive dossiers (CTD/ACTD) for registration of pharmaceutical products in international markets.
- Manage post-approval changes and variations in accordance with regulatory requirements.
- Act as a liaison with global regulatory agencies to address queries and ensure compliance.
- Stay updated with the latest regulations and guidelines issued by EU, MHRA, WHO, and other relevant regulatory bodies.
- Maintain accurate and up-to-date regulatory documentation.
Qualifications & Experience Required:
- Education: B.Pharm / M.Pharm / M.Sc (Chemistry / Microbiology).
- Experience: 2–10 years of relevant experience in a pharmaceutical manufacturing environment, preferably in EU-GMP / MHRA-approved plants.
- Knowledge: Strong understanding of current regulatory guidelines and GMP principles.
- Skills: Excellent communication, documentation, and problem-solving skills. Ability to work independently and as part of a team.
Benefits:
- Competitive salary package commensurate with experience and qualifications.
- Performance-linked incentives to reward outstanding contributions.
- Comprehensive medical and accidental insurance coverage.
- Subsidized canteen and transportation facilities for employee convenience.
- Continuous training and development opportunities to enhance skills and knowledge.
- Exposure to global standards and best practices in pharmaceutical manufacturing.
How to Apply:
If you are a motivated and qualified individual looking for a challenging and rewarding career opportunity, we encourage you to apply. Please send your updated CV to [email protected]
Subject Line: Application for [Department] – [Your Name]
Example: Application for Quality Control – Rahul Sharma
Applications will be reviewed on a rolling basis, and shortlisted candidates will be contacted for interviews. We look forward to hearing from you!
Frequently Asked Questions (FAQs):
1. Is prior experience in EU-GMP or MHRA-approved plants mandatory?
While experience in EU-GMP or MHRA-approved plants is preferred, we also encourage candidates with strong experience in WHO-GMP/USFDA plants and a demonstrated willingness to learn international standards to apply.
2. What is the location of Mepro Pharmaceuticals Unit-III?
The facility is located in Vadodara (Baroda), Gujarat.