Regulatory Affairs Job Vacancies at Mepro Pharmaceuticals

Regulatory Affairs Job Vacancies at Mepro Pharmaceuticals | B Pharm/M.Pharm | 1-16 Years Experience | Vadodara, Gujarat

Apply now for Regulatory Affairs jobs at Mepro Pharmaceuticals (B Pharm/M.Pharm) – 1 to 16 years experience – Vacancies in Vadodara, Gujarat

Regulatory Affairs Career Opportunities at Mepro Pharmaceuticals – Vadodara, Gujarat

Mepro Pharmaceuticals Pvt. Ltd. (Unit-III), a reputed name in pharmaceutical manufacturing and regulatory compliance, is inviting experienced professionals to join its Regulatory Affairs team at Vadodara, Gujarat. Candidates with B Pharm or M.Pharm qualifications and 1 to 16 years of experience are encouraged to apply for multiple positions across seniority levels. This is an excellent opportunity to contribute to a globally compliant, growth-oriented organization.

Why Join Mepro Pharmaceuticals?

• Global Exposure: Engage in regulatory submissions across TGA, Europe, and other global markets.
• Work on CTD/ACTD Formats: Gain expertise in complex regulatory formats for both injectable and oral solid dosage (OSD) forms.
• Career Growth: Opportunities to manage the full lifecycle of regulatory activities.
• Collaborative Environment: Work cross-functionally with R&D, QA, Production, and Validation teams.

Current Openings in Regulatory Affairs – Unit III

Assistant/Deputy Manager – Regulatory Affairs (Injectable)

Responsibilities:

• Review and submission of injectable product dossiers for TGA and Europe.
• Handle global regulatory compliance in CTD/ACTD formats.
• Manage lifecycle activities and respond to regulatory authority queries.

Qualifications:

• B Pharm or M.Pharm
• Experience: 10 to 16 years

Assistant/Deputy Manager – Regulatory Affairs (OSD)

Responsibilities:

• Prepare and submit OSD product dossiers.
• Lead lifecycle management and respond to regulatory queries as per ICH guidelines.
• Ensure global compliance with country-specific requirements.

Qualifications:

• B Pharm or M.Pharm
• Experience: 10 to 16 years

Officer/Sr. Officer/Executive – Regulatory Affairs (Injectable)

Responsibilities:

• Support dossier submission in CTD format for injectable development.
• Coordinate with teams for CMC documentation.
• Ensure systematic document tracking and compliance.

Qualifications:

• B Pharm or M.Pharm
• Experience: 1 to 4 years

Officer/Sr. Officer/Executive – Regulatory Affairs (OSD)

Responsibilities:

• Prepare country-specific and ACTD/CTD dossiers.
• Assist in global tender documentation and lifecycle management.
• Review and compile technical documents.

Qualifications:

• B Pharm or M.Pharm
• Experience: 1 to 4 years

How to Apply

📩 Send your updated CV to hr3@mepro.in with the subject line: RA9062025

🕒 Join a company committed to quality, compliance, and innovation in the pharma sector.

Quick Overview Table

Company Name	Mepro Pharmaceuticals Pvt. Ltd.
Vacancies in Departments	Regulatory Affairs – OSD & Injectable
Required Education	B Pharm / M.Pharm
Experience Required	1 to 16 Years
Location	Vadodara, Gujarat