Joyce Elkins

Medical Devices

Joyce Elkins is a skilled professional, that works in Southwest Technologies on the position of Qa and Ra Manager since 2015. Joyce has earned professional experience in more than eight positions at different companies. Joyce Elkins went to the University of Nebraska at Kearney and got education from 1991 to 1997. Joyce Elkins has the following qualifications: Quality Engineer, Asq, License 7825, and License 7825. Springfield, Missouri is the area, where the professional was lastly known to live. Their phone number and email are accessed through SoftwareOfficial on demand.
Name variants:
Joy Elkins
Last updated May 29, 2024

Contact Information

Last Update
Jun 22, 2022
Email
jo**@xyloscorp.com
Location
Springfield, MO
Company
Southwest Technologies

Workplace

Qa and Ra Manager

Work History

Qa and Ra Manager

QA/RA Manager of the Quality Management System. Audit lead for 2014 audits for NSF and FDA as well as for Kosher and Halal certifications. Lead the company’s first FDA audit (no observations...
Nov 2015 — Mar 2017

Qa Manager

Mar 2014 — Jan 2015

Director Quality Assurance and Regulatory Affairs

2747 southwest 6Th St, Redmond, OR 97756
Established and performed training for both Product Development & RAQA staffs in a variety of topics, Design Development, 510(k) submissions, Risk Management, utilization of Industry Standar...
Jun 2011 — May 2014

Director Quality Systems and Regulatory Affairs

Pennsylvania
Wrote and received approval for 5 different 510(k) products. Significantly reduced dose auditing costs via VD MAX. Established a Risk Management system and a new Design Control process. Wrot...
2008 — May 2011

Director Quality Systems and Regulatory Affairs

345 east Main St #p/o box 708, Warsaw, IN 46580
Oversaw the development and of the first approved 510(k) in 10 years and followed by four more in the next three years Implemented a Risk Management system (rated as Zimmer Best Practice) ...
2004 — 2008

Director of Quality Assurance and Regulatory Affairs

Significantly revised and upgraded CAPA program. Reduced LAL testing with annualized savings of $300K. Implemented an inspection reconfiguration program that reduced floor inspection manning...
2001 — 2004

Director Quality Assurance and Regulatory Affairs

5960 Heisley Rd, Mentor, OH 44060
Responsible for, designing, implementing and directing the activities associated with Regulatory Affairs and Quality Systems of 16 custom Sterilization Facilities. Evaluate facilities abilit...
1998 — 2001

Quality Assurance and Sterilization Manager

California
Responsible for the activities of 80+ employees including 3 microbiologists, 5 quality engineers and 2 supervisors. Responsible for management of the Sterilization process including its pers...
1987 — 1998

Occupations

Executive
Manager
Quality Manager
Team Leader
Operations Manager
Managers

Skills

Quality System
Capa
Fda
Medical Devices
Quality Assurance
Iso 13485
Design Control
Quality Control
Regulatory Affairs
V&V
Iso
Sterilization
Quality Auditing
Change Control
Regulatory Requirements
Spc
Microbiology
Root Cause Analysis
Quality Management
Fda Gmp
Lean Manufacturing
Sop
Astm Standards
Gamma
Asq Senior Member
Jit
Ce Marking
Tuv
Mdrs
Team Building
Statistical Sampling
Microsoft Office
510 K
Eto
Eu Notified Bodies
Aami
Design History
Operational Risk Management
Bsi
Tno
Cfr 820
Mba
W Beam Sterilization
Disposable Medical Devices
Techinical Files
Master Device Listings
Raqa
Qsr
Safety
Doh
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