About Company:
We are a privately owned pharmaceutical manufacturer and associated with the best pharmaceutical companies world-wide Over 3 decades of experience in manufacturing of tablets, capsules, creams/ointments and sterile injectables State-of-the-art manufacturing facilities, pool of diligent employees and niche products We employ over 1000 people under our parent company and have a sales turn-over of over 35 million USD across 3 different manufacturing locations, covering a total of 300,000 sq.ft of constructed area Approvals of UK, MHRA and PIC/S nations besides governing bodies of many other countries
Website
http://www.mepro.in
Vacancy Details:
Job Description:
Hiring Alert – Mepro Pharmaceuticals Pvt. Ltd. (Unit-III, Vadodara)
We are looking for experienced professionals to join our Regulatory Affairs (RA) team at Mepro Pharmaceuticals Pvt. Ltd. (EU-GMP approved facility, Vadodara).
Open Position:
Deputy Manager / Assistant Manager – Regulatory Affairs (RA)
Job Responsibilities:
1. Prepare, review, and submit regulatory dossiers for various international markets (EU, ROW).
2.Ensure compliance with global regulatory guidelines.
3.Coordinate with internal teams for documentation and query responses.
4.Handle regulatory audits and provide necessary support.
5.Stay updated with evolving regulatory requirements and implement necessary updates.
Requirements:
Qualification: B. Pharm / M. Pharm
Experience: 10+ years in Regulatory Affairs (preferably in a pharmaceutical company).
Strong knowledge of regulatory guidelines (EU-GMP, MHRA, TGA, etc.).
Excellent communication and documentation skills.
Location: Vadodara, Gujarat
Interested candidates can share their resumes at hr3@mepro.in
Join us and contribute to our success!
Aakash Kachhiya Vijaysinh Rathod