We found the following information about Harlow Thielke at Oriel Stat A Matrix, where this expert has worked as a Director of Quality Training and Consulting since 2019. Harlow's total work experience is over 15 years, during which time they had at least four jobs at different places to develop professional skills. Harlow studied at the St. Cloud State University from 2011 to 2013. Harlow Thielke currently lives in Chaska, Minnesota. You can contact with Harlow by searching for phone or email or get further info by requesting access to Harlow's additional details from SoftwareOfficial.
Name variants:
Harlow Thielke
Last updated May 17, 2024
Contact Information
Workplace
Director of Quality Training and Consulting
Edison, NJ
Industry
Management Consulting
Colleagues
Work History
Director of Quality Training and Consulting
1095 Morris Ave SUITE 103B, Union, NJ 07083
Oriel STAT A MATRIX helps organizations reduce costs and risk by achieving compliance with global regulations and improving business processes. The company’s consultants and trainers provide...
from Oct 2019
Regulatory Affairs and Qms Coordinator
Eden Prairie, MN
Starkey Hearing Technologies is a privately held, global hearing technology company headquartered in Eden Prairie, Minn. We are recognized for our innovative design, development and distribu...
May 2007 — Sep 2017
Quality Engineer and Qms Coordinator
Managed the Antares Pharma medical device project for QMR. Included the buying and planning of product components, coordination and scheduling of production, and design, implementation and m...
Apr 2002 — May 2007
Education
2011 — 2013
2006 — 2007
Occupations
Executive
Director
Management Consultant
Owner
Operations Manager
Management Analyst
Analysts
Chief Executive
Skills
Iso 13485
Medical Devices
Quality System
Fda
Regulatory Affairs
Iso
Lean Manufacturing
Regulatory Documentation
Process Improvement
Product Development
Design Control
Electronics
Iso 14971
Cross Functional Team Leadership
Internal Audit
Project Management
Biomedical Engineering
Process and Procedure Design
Technical Files
External Audit
Toastmasters
Team Leadership
Capa
Manufacturing
Change Control
Continuous Improvement
International Medical Device Regulations
Iso Standards
Fda 21 Cfr 820
Med Dev Technical File