Arni Medica is a leading medical device manufacturer specializing in contract manufacturing, new product development, and high-quality production of nephrology and healthcare products. We are looking for motivated and detail-oriented fresh graduates to join our Regulatory Affairs (RA) team. This role offers exposure to medical device regulations, product registrations, technical documentation, and compliance processes.

Requirements
• Assist in preparation and compilation of regulatory dossiers for medical devices.

• Support product registration and licensing activities with regulatory authorities (CDSCO and other global markets).

• Maintain and organize technical documentation, Device Master Files (DMF), and regulatory records.

• Ensure compliance with applicable regulatory standards and guidelines.

• Assist in Labelling review, IFU (Instructions for Use), and artwork compliance checks.





• Support change control documentation and regulatory impact assessments.

• Coordinate with QA, R&D;, and production teams for regulatory submissions.

• Track regulatory submissions, approvals, and renewals.

• Assist in handling queries from regulatory bodies and auditors.

• Maintain regulatory databases and ensure timely updates.

Skills Required:

• Basic knowledge of medical device regulations and documentation

• Understanding of ISO 13485 and regulatory compliance (preferred)

• Robust attention to detail and documentation skills

• Good communication and coordination abilities

• Willingness to learn regulatory processes and global requirements

📌 Jr RA Executive (Hyderabad)
🏢 Arni Medica
📍 Hyderabad