Walk|In Interviews for Regulatory Affairs | Avantika Medex Pvt| Ltd |on 11th

As a 100% export-oriented unit (EOU) with a backward-integrated production facility for pharmaceutical tablets, capsules, ointments, sachets, and injectables, Avantika Medex Pvt. Ltd. Our company, Avantika Medex Pvt. Ltd., has a growth rate of more than 50% year over year and is a member of a group of firms with a 150+ Crore turnover.

Job Description : Regulatory Affairs Officer/Sr. Officer/Executive:

Avantika Medex Pvt. Ltd is currently seeking motivated individuals to join our Regulatory Affairs team. The positions available are for Officer, Senior Officer, and Executive levels. As part of the Regulatory Affairs Department, you will play a crucial role in ensuring compliance with regulatory requirements for our pharmaceutical products. The job details are as follows:
• Job Title: Regulatory Affairs Officer/Sr. Officer/Executive
• Department: Regulatory Affairs
• Number of Positions: 06
• Job Location: Ahmedabad

Responsibilities:
• Prepare and submit regulatory documents including product registration dossiers, variations, and renewals, to regulatory authorities in compliance with local and international regulations.
• Review and analyze scientific data, literature, and other relevant information to support regulatory submissions.
• Stay updated with changes in regulatory guidelines and requirements, and communicate the impact on the company’s products and processes.
• Collaborate with cross-functional teams, including R&D, Quality Assurance, and Production, to ensure regulatory compliance throughout the product lifecycle.
• Prepare and maintain product labeling, packaging, and promotional material in accordance with regulatory standards.
• Assist in conducting internal audits and inspections to ensure compliance with regulatory standards and guidelines.
• Respond to queries and requests from regulatory authorities regarding submitted applications.
• Monitor and track regulatory approvals and maintain necessary documentation for regulatory compliance.

Requirements:
• Education: B.Pharm or M.Pharm degree from a recognized university.
• Experience: 1 to 6 years’ experience in regulatory affairs within the pharmaceutical industry.
• Sound knowledge of pharmaceutical regulations, including but not limited to drug registration, labeling requirements, and post-approval commitments.
• Familiarity with regulatory guidelines from authorities such as the FDA, EMA, or other relevant regulatory bodies.
• Strong attention to detail and the ability to effectively prioritize tasks to meet deadlines.
• Excellent written and verbal communication skills.
• Proficient in using computer software applications, including Microsoft Office.
• Ability to work both independently and collaboratively in a team environment. Walk-in details:Avantika Medex Pvt. Ltd. is conducting a walk-in interview for interested candidates on 11-06-2026. The interview will be held from +:00 AM to 12:00 PM at the following venue:

Venue: Avantika Medex Pvt. Ltd. Plot: J8 to J11, Gallops Industrial Park-2, Chacharwadi, N.H 8A, Ta: Sanand, Dist.: Ahmedabad-382213.

To express your interest in the position, you are required to send your detailed resume to hr@avantikamedex.com or contact the provided phone number, +62484+118 (WhatsApp only). It’s important to note that they prefer communication through WhatsApp rather than phone calls.

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