Job Title:
Engineer II, Med Devices

Req #:
4322BR

Job Description:
Provide technical leadership for GO&E Engineering projects. Provide Electro/Mechanical leadership for Automation development for new contact lens programs (PAQ CIP and PureVision, etc) which is crucial for new product development. Lead a multi-discipline, cross-functional team environment. Interface with internal and external customers while working on key new product programs for 2008 and 2009. Facilitate internal resources and outside vendors in developing technical solutions for primary and secondary automated equipment used in the production of medical devices/instruments. Support process and equipment integration activities through Manufacturing Validation. Work in conjunction with Process Engineering, develop Functional requirements for manufacturing ready equipment. Establish acceptance criteria for both pre and post delivery

Qualifications
. Provide manufacturing training support, spare part identification, documentation package creation and preventative maintenance procedure development for custom-built equipment. Create and implement project schedules in order to meet overall program goals. Qualifications BS/MS in Mechanical Engineering, Engineering Technology or equivalent experience. 5-7 years experience in process automation and equipment build with experience in design, build, debug and systems integration of custom built systems and medical products. Computer literate. Experience in high volume low cost manufacturing systems development desired. Experience with process automation integration of PLC controlled machines a plus. Hands-on experience and technical knowledge of fully automated precision material handling systems required. Knowledge of SPC, DOE and statistical analysis a plus. Experience with medical device or clean room environment a plus. Design and machining abilities a plus. Use and knowledge of Lean and DFSS tools desired. Must be able to work with Manufacturing/Maintenance technicians and engineers in a team setting. ISO-9000, GMP, medical device manufacturing experience.

Work Location NY - Rochester-1400 N Goodman Street Relocation Available Yes

Status Full-Time