...their experience considering the rapid nature of updates/changes in the regulatory landscape, the device, its functionalities, and the therapy area.
Preferred Experience:
1. Significant experience writing s...
...hand as there is an exciting opportunity waiting for you as “RA Specialist” with us. "Apply now" - At Novo Nordisk, we assure you will... ...SME for the defined area of responsibility. Mentor...
...environment? Are you best at what you do? If so, raise your hand as there is an exciting opportunity waiting for you as “Senior Regulatory Professional” with us. "Apply now" - At Novo Nordisk, we assure you will exp...
...scale across value chain on core regulatory processes across NN product portfolio. We provide regulatory expertise in terms of CMC & Medical Devices, Combination Products and work very closely with our colleagues in...
...Device Regulation (EU MDR) and various FDA guidance Pre-market submission guidelines, General Principles of Software Validation, Off The Shelf (OTS a.k.a SOUP) software use, Software as a Medical Device: Clinical Ev...
...Electrical Engineering or similar field
• Minimum of 5 years of relevant work experience in software engineering or quality engineering in medical device development
• Looking for work experience in software quali...
Designation : Test Lead Engineer
Primary Skills - Medical Device , Device testing Experience in JIRA, Automation Testing , Embedded Device Testing • 7+ years of software testing experience
• Experience in Medical dev...
...We are looking for a dynamic biomedical technician to join our biomedical department. In this role, you'll be in charge of overseeing the care and use of all biomedical equipment, performing machinery repairs, and t...
Role : Regulatory Manager
Work Location : Bangalore
Key Responsibilities & Accountabilities (Tasks & Deliverables):
General and Task... ...Provides leadership and guidance (including training) t...
...Job Title: QARA Specialist
Job Role :
The Quality and Regulatory Affairs (QARA) Specialist will provide leadership in the quality and regulatory affairs function to understand regulatory requirements of medic...
