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Career Diaries by Elemed

How having a background in general management and operations can change and help your perception as a regulatory affairs professional | Thomas Meininghaus, Vice President of Regulatory Affairs at Ottobock

April 13, 2021 Elena Kyria Episode 15
Career Diaries by Elemed
How having a background in general management and operations can change and help your perception as a regulatory affairs professional | Thomas Meininghaus, Vice President of Regulatory Affairs at Ottobock
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Career Diaries by Elemed
How having a background in general management and operations can change and help your perception as a regulatory affairs professional | Thomas Meininghaus, Vice President of Regulatory Affairs at Ottobock
Apr 13, 2021 Episode 15
Elena Kyria

Key takeaways:

  • How a different background can ENRICH your perception as a Regulatory Affairs professional
  • DISCOVER the thin divide between Management and Regulation in Medtech and why it matters
  • The BEST piece of advice that Thomas received in his career
  • Why you should be focused on the BIG PICTURE


About Thomas Meininghaus, VP RA at Ottobock:
Thomas has been the Vice President for Global Regulatory Affairs at Ottobock since February 2019. He’s in charge of their Legal Manufacturer as well as 200 Patient Care Clinics.

He is a highly regarded, visionary and culturally sensitive business executive. Combining his engineering background (PhD) with strong commercial and quality expertise, he has a demonstrable track record of developing and implementing business strategy for medical device organisations in both the corporate and SME environment. 

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Show Notes

Key takeaways:

  • How a different background can ENRICH your perception as a Regulatory Affairs professional
  • DISCOVER the thin divide between Management and Regulation in Medtech and why it matters
  • The BEST piece of advice that Thomas received in his career
  • Why you should be focused on the BIG PICTURE


About Thomas Meininghaus, VP RA at Ottobock:
Thomas has been the Vice President for Global Regulatory Affairs at Ottobock since February 2019. He’s in charge of their Legal Manufacturer as well as 200 Patient Care Clinics.

He is a highly regarded, visionary and culturally sensitive business executive. Combining his engineering background (PhD) with strong commercial and quality expertise, he has a demonstrable track record of developing and implementing business strategy for medical device organisations in both the corporate and SME environment.