Making it in Manufacturing

Carsten Jasper: Revolutionising Pharma Compliance with AI, Cleanrooms & Bold Thinking


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In this episode, we are joined by Carsten Jasper, a globally recognised leader specialising in pharmaceutical quality, regulatory compliance, and digital transformation within life sciences.


  • Carsten leads Quality & Compliance within Charles River’s R&D division, where he oversees risk management and the validation of regulated systems.
  • With 20 years of experience across in-vitro diagnostics, aseptic manufacturing, and total quality management, he brings deep regulatory and operational expertise.
  • He also runs Jasper Consulting and contributes to PTS Training Service, developing AI-powered tools such as VR/AR simulations and digital twins for cleanroom training.
  • Previously, he held senior roles in diagnostics and chemical technology and is a regular industry speaker, most recently presenting on AI in cleanroom design at a leading Life Sciences engineering conference.


In this episode, we discuss a range of topics including CSV Validation, Risk Management, Data Integrity, AI, Auditing, Advice for Candidates and more. This conversation applies broadly to all types of connections in the Life Sciences Industry, and aims to educate and inspire those who want to excel in the manufacturing and engineering space.


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Carsten Jasper

Senior Director, QRM and CQV (R&D)

LinkedIn: https://www.linkedin.com/in/carsten-jasper-59189982/


Thomas McMann

Director - Contracts Division at ARTO

LinkedIn: https://www.linkedin.com/in/thomas-mcmann-05540a10b/


Timestamps:

00:00 Career Beginnings

10:09 CSV Validation & Risk Management

15:13 Data Integrity & AI

23:53 Auditing

31:54 Rounding Up


#MakingItInManufacturing #ARTOTalent #ManufacturingAndEngineering #ISPE #AI #OPEX #CDMOS #DataIntegrity #Auditing #CSV

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Making it in ManufacturingBy ARTO Talent