Technical Specialist - MDR, ISO 13485, MDD

Experience: Not Available to Not Available years

Location: Chennai, India

Skills: medical device regulation (mdr), iso 13485, medical device directive (mdd), regulatory requirements, analytical skills, problem-solving skills, interpersonal abilities, detail oriented

Job Summary
The Technical Specialist will be responsible for tasks related to mdr, ISO 13485, and MDD. The primary responsibilities include ensuring compliance with relevant regulations and standards in the medical device industry.

Key Responsibilities
1. Implement and maintain processes to ensure compliance with medical device regulation (mdr), iso 13485, and medical device directive (mdd)
2. Provide expertise and guidance on regulatory requirements for medical devices
3. Collaborate with cross functional teams to assess and address regulatory compliance issues
4.



Conduct internal audits to identify areas for improvement and ensure adherence to standards
5. Stay updated on changes in regulations and standards related to medical devices

Skill Requirements
1. Proficiency in medical device regulation (mdr), iso 13485, and medical device directive (mdd)
2. Robust understanding of regulatory requirements in the medical device industry
3. Excellent analytical and problem-solving skills
4. Effective communication and interpersonal abilities
5. Detail oriented with a focus on accuracy and compliance

Other Requirements
1. Relevant certifications in medical device regulations or ISO standards are a plus

📌 Technical Specialist MDR, ISO 13485, MDD (Chennai)
🏢 HCL Technologies
📍 Chennai