Resumes
Resumes
Lynn Couchon
View pageLynn Couchon North Kingstown, RI
View pageWork:
Isis Biopolymer, Inc
Providence, RI
Jun 2008 to Nov 2011
Medical Device Designer / Documentation Coordinator
Parlex Corporation
Cranston, RI
Jan 2002 to Jun 2008
Design Department Lead
Parlex Corporation
Cranston, RI
Apr 1992 to Jun 2008
Senior Designer
Independent Energy, Inc
East Greenwich, RI
Sep 1984 to Jan 1992
Designer / Drafter
Providence, RI
Jun 2008 to Nov 2011
Medical Device Designer / Documentation Coordinator
Parlex Corporation
Cranston, RI
Jan 2002 to Jun 2008
Design Department Lead
Parlex Corporation
Cranston, RI
Apr 1992 to Jun 2008
Senior Designer
Independent Energy, Inc
East Greenwich, RI
Sep 1984 to Jan 1992
Designer / Drafter
Education:
New England Institute of Technology
Warwick, RI
Jan 1982 to Jan 1984
A.S., Electro-Mechanical Drafting and Design
Warwick, RI
Jan 1982 to Jan 1984
A.S., Electro-Mechanical Drafting and Design
Skills:
Medical Device Designer for Transdermal Drug Delivery Systems. Documentation Coordinator responsible for creation and implementation of Quality System. Responsible for all aspects of Quality System Management including but not limited to Documentation Control, Change Control, and Records for Medical Device manufacturer, in preparation of [] and ISO9001 Certifications. Project Manager responsible for implementing Design Reviews with representatives from all departments and coordinating Design Input, Output, Verification and Validation activities. Electro-mechanical designer supporting the manufacture of Printed Flexible Circuits for the Appliance, Medical, Automotive, RFID, and Telecommunications Industries. Designer of Printed Circuit Boards, Plastic Enclosures, Labeling, and Technical Manuals for heating, cooling and solar control manufacturer. Organized and/or participated in New Product Development, Design Review and Documentation Change Control Teams. Created and documented Design Guidelines for medical, appliance, telecommunication, and computer peripheral markets. Support of successful site certification to ISO [] and ISO 13485. Trained and supervised Designers. Trained manufacturing personnel in GMP practices and ISO 13485 "In Our Company". Software experience includes: Pads for circuit design, CamMaster for Gerber editing CNC, and Laser programming, AutoCad for tooling and assembly drawings, Adobe Illustrator, Photoshop, Acrobat, Microsoft Office, MRP and Access Database Applications. Knowledgeable, with limited experience - Solidworks, Enterprise PDM and 3D Via.