Senior manufacturing engineer at Medica Corp
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Posted by: "brian ikemoto" bikemoto@verizon.net bikemoto@verizon.net
Sun Jul 12, 2009 8:35 pm (PDT)
My name is Brian Ikemoto and I'm a manufacturing engineer. Here is a job lead for a senior manufacturing engineer at Medica Corp with whom I interviewed, received an offer, but declined. If you meet the listed qualifications and are interested in this position, please contact the operations manager Joe Traut (jtraut@medicacorp.
Medica, an FDA Class II designer and manufacturer of in-vitro diagnostic devices, is seeking a highly resourceful Senior Manufacturing Engineer. The ideal candidate is a technically-
Responsibilities:
· Resolves manufacturing problems by applying technical
knowledge and skills. Escalates design, manufacturing, and product test issues to others within the organization when appropriate.
· Continuously improves quality, lead-time,
productivity, and cost of existing products and processes.
· Designs, implements, and qualifies new or modified
designs, processes, and manufacturing/
· Participates in the New Product Introduction (NPI)
process by performing Design for Manufacturability (DFM) and Design for Cost (DFC) analysis of prototype products.
· Provides support to Purchasing, Quality, and R&D Departments
during vendor qualifications and evaluations, including vendor audits.
· As a key Material Review Board member, resolves
nonconformities by using corrective and preventive action techniques.
· Supervises and mentors junior team members as
required.
Requirements:
· B.S. in Engineering or related technical discipline
with 5-8 years experience in medical device manufacturing is required.
· A proven track record generating and leading cost
reduction and product improvement initiatives through validation and release is required.
· Strong leadership and organizational skills with a
demonstrated ability to lead cross-functional teams is required.
· Working experience with Pro/ENGINEER 2001 or an
equivalent CAD system is required.
· Proficiency with Microsoft Office Applications
(Excel, Word, and Outlook) is required.
· MRP software experience is desirable.
· Knowledge of statistical techniques and the ability
to plan and implement projects from concept to completion is required.
· Knowledge of metal and plastic design requirements
and fabrication techniques is required.
· Working knowledge of FDA/ISO regulatory guidelines is
required.
· The candidate must be highly motivated, hands-on,
innovative, able to work with minimal direction, and should have good problem solving, teamwork, and oral and written communication skills.
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