Linda Heth

IT Associate Director - PLM/CAE, ZimmerBiomet

IT Associate Director with a demonstrated history of leading organizational transformation using PLM and integrated systems to advance business collaboration and agility. Progressive leadership positions in Design, Engineering, Quality, Technical Services and IT in Professional Tools, Automotive and Medical Device industries. Skilled in Computer-Aided Design (CAD), Value Stream Mapping, Failure Mode and Effects Analysis (FMEA), ISO/TS 16949, ISO 13485 and Quality Management. Strong Engineering Professional

Tell Us Something Interesting:

Just went live with my first PLM implementation in the Medical Device Industry after serving in Automotive for over 21 years. ZimmerBiomet implemented a Regulatory Information Management System (RIMS) with integrations to Master Data, UDI and Global Trade. Successful Day 1!!!

Session Track: Life Sciences

Tuesday, June 11 2:15 PM - 3:00 PM 209

LS113P - Preparing for EU-MDR: Insights from Medical Device Leaders

The medical device industry is facing a wave of regulatory challenges, including EUMDR, GDPR, and Single Audit Program (MDSAP). The EUMDR 2020 deadline for the first wave of devices is rapidly approaching, and companies are moving from planning to action. Learn how life sciences leaders are rising to the challenge in this panel discussion. Panelists will explore a range of approaches for tackling common compliance challenges and highlight similarities and differences across companies.

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