APDM Pharmaceuticals Hiring Regulatory Affairs Specialist (02 Posts)

APDM Pharmaceuticals Pvt. Ltd. is hiring experienced professionals for regulatory affairs positions as the company expands its presence in global markets.

Job Title: Regulatory Affairs Specialist
Number of Positions: 02
Location: APDM Pharmaceuticals Pvt. Ltd, Unit No. 90-91, Parishram Industrial Hub, Chacharvadi, Vasna, Changodar, Gujarat 382213

Vacancy Overview

APDM Pharmaceuticals is looking for experienced regulatory affairs professionals to focus on regulatory compliance in the US and EU markets. The company offers excellent career growth opportunities.

Experience & Qualifications

• Experience: 2-5 years of regulatory affairs experience in regulated markets like the US and EU, preferably in a pharmaceutical company or service provider. (Freshers are not eligible.)
• Qualification: Bachelor’s degree in Life Sciences is required. M Pharma is highly preferred.

Key Responsibilities

• Regulatory Submissions: Ensure timely and accurate submissions to US and EU regulatory authorities.
• Compliance Management: Oversee adherence to all regulatory requirements for pharmaceutical products.
• Documentation: Prepare, review, and submit regulatory documents, dossiers, and filings.
• Communication: Act as a liaison with regulatory bodies, providing clear reports and updates.
• Cross-functional Coordination: Work with internal teams like Quality Assurance, Research & Development, and Production to ensure compliance with regulatory standards.

How to Apply

Submit your resume via email to hr@apdmpharma.com if you meet the qualifications.