Medical Device Regulatory Operations Associate

E Merge tech; Chennai District; On-site; INR 700,000 - 1,500,000; Full time

Job summary

E Merge tech in Chennai, India, is seeking an experienced regulatory affairs professional to manage medical device regulatory operations and ensure timely compliance with global standards. You will develop and implement regulatory strategies, review submissions, and collaborate with cross-functional teams to resolve issues and improve processes.

The role requires proactive communication, meticulous documentation, and staying up-to-date with evolving regulations.

Responsibilities

• Manage and coordinate medical device regulatory operations activities.
• Develop and implement effective regulatory strategies to ensure compliance with industry standards.
• Collaborate with cross-functional teams to resolve regulatory issues and improve processes.
• Conduct thorough reviews of regulatory documents and submissions.
• Provide training and guidance on regulatory requirements to internal stakeholders.
• Stay up-to-date with changing regulatory requirements and industry trends.

Job description

• Manage and coordinate medical device regulatory operations activities.
• Develop and implement effective regulatory strategies to ensure compliance with industry standards.
• Collaborate with cross-functional teams to resolve regulatory issues and improve processes.
• Conduct thorough reviews of regulatory documents and submissions.
• Provide training and guidance on regulatory requirements to internal stakeholders.
• Stay up-to-date with changing regulatory requirements and industry trends.

Disclaimer: This job posting & Location 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.