Develop and implement regulatory strategies for medical devices.
Prepare and submit regulatory documents to relevant authorities.
Conduct thorough reviews of regulatory submissions to ensure accuracy and completeness.
Collaborate with cross-functional teams to meet regulatory requirements.
Stay updated with changing regulatory requirements and guidelines.
Provide training and guidance on regulatory matters to internal stakeholders.

Job Requirements
Solid knowledge of regulatory affairs and compliance.
Experience with CDSCO, CE, ISO 13485 regulations.
Excellent communication and project management skills.
Ability to work independently and as part of a team.
Solid analytical and problem-solving skills.
Familiarity with medical device industry regulations and standards.

Disclaimer: This job posting has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.

📌 Regulatory Expert Mumbai
🏢 Carenx Innovations
📍 Mumbai