Supervisor, Regulatory Affairs
Thermo Fisher Scientific is seeking a Regulatory Affairs Supervisor to lead market access teams for IVD and Medical Device portfolios. The role involves driving global regulatory strategy, managing complex submission lifecycles, and collaborating with cross-functional teams like R&D and Quality. You will ensure compliance with frameworks such as MDR, IVDR, and FDA requirements while mentoring junior staff. This is a senior-level position based in Bengaluru requiring extensive experience in regulatory documentation and health authority interaction.
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Experience
12+ years
Function
Engineering
Work mode
Onsite, India
Company
Tier 1
What you will work on
Thermo Fisher Scientific is seeking a Regulatory Affairs Supervisor to lead market access teams for IVD and Medical Device portfolios. The role involves driving global regulatory strategy, managing complex submission lifecycles, and collaborating with cross-functional teams like R&D and Quality. You will ensure compliance with frameworks such as MDR, IVDR, and FDA requirements while mentoring junior staff. This is a senior-level position based in Bengaluru requiring extensive experience in regulatory documentation and health authority interaction.
TAL's take
High-caliber global company with a well-defined leadership role in a specialized domain.
The JD clearly defines responsibilities, domain focus (IVD/Medical Devices), and leadership expectations.
Salaries at Thermo Fisher Scientific
17.4 LPA average
Based on 13 Grapevine salary entries for Thermo Fisher Scientific.
Engineering
16 - 18 years | L7
38 LPA average
Range: 38 - 38 LPA
Finance
0 - 2 years | Contractor
3 LPA average
Range: 3 - 3 LPA
Other roles
0 - 2 years | Contractor
9 LPA average
Range: 9 - 9 LPA
Other roles
2 - 4 years | L5
13 LPA average
Range: 13 - 13 LPA
Must haves
- 12+ years experience in global Regulatory Affairs for IVDs and Medical Devices
- Proven track record in hands-on submission execution and authority communication
- Strong understanding of MDR, IVDR, FDA 510(k)/PMA regional pathways
- Experience managing simultaneous submissions across multiple geographies
- Excellent technical writing and analytical skills
Tools and skills
About the company
Global leader in scientific research and healthcare solutions.
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