Modify Search

Medical Device Subject Matter Expert

Tech Mahindra Limited
Hyderabad / Secunderabad
10-15 years
Not Specified

Minimal 10 years working experience in the field of medical devices through positions in industry, consultancy or regulatory agencies (Notified Bodies, FDA, EMA), in either manufacturing, R&D, quality or regulatory roles

Skills :

This rol is responsible for facilitating the efficient execution of all assigned Quality Compliance project activities and will support the Commercial Product Quality (CPQ) executing LD Post Market Surveillance Procedures.

Skills :

Quality Professional

Siemens Technology
Bengaluru / Bangalore India
Not Specified
Not Specified

Job Description : Create, Review, Quality Technical Documentation related to IVDR Post Market Surveillance Plans, Post Market Surveillance Reports, Post Market Performance Follow Up Plans, Post Market Performance Follow Up Reports, Periodic Safety

Skills :

Quality Professional

Siemens Technology
Bengaluru / Bangalore India
Not Specified
Not Specified

Job Description : Create, Review, Quality Technical Documentation related to IVDR Post Market Surveillance Plans, Post Market Surveillance Reports, Post Market Performance Follow Up Plans, Post Market Performance Follow Up Reports, Periodic Safety

Skills :

Sr. Manager - Regulatory Affairs

Siemens Technology
Vadodara India
5-7 years
Not Specified

Job Description : Job Summary: ​ Candidate should have experience in Regulatory, , ​quality inspection, auditing and process as per in country regulations and export markets. Responsibilities & Duties: 1. Interpret and implement quality assuran

Skills :

Quality Specialist

Danaher
Bengaluru / Bangalore India
10-13 years
Not Specified

Job Title: Quality Specialist Job location - Bangalore, India Radiometer, our mission is to help caregivers make diagnostic decisions that save lives. To provide caregivers the insight and confidence that help them arrive at the right diagnostic dec

Know more