MEMS-Semiconductor Maintenance and Repair Technician
The individual will perform scheduled intermediate level maintenance and repair work on facilities and various MEMS/semiconductor fabrication equipment. This includes overhauling, repairing or rebuilding of assemblies, subassemblies, and circuits to the component level when required. This position requires detailed troubleshooting, thorough documentation of work performed, and detailed testing and qualification/validation of repairs. Primary responsibilities will be maintaining high vacuum deposition and silicon etch (RIE) systems, photolithography and anodic bonding tools, and some metrology equipment. This job involves working mainly in a clean-room environment, where appropriate garments have to be worn.
Qualifications
- A minimum of 2 years hands-on experience repairing and maintaining facilities and electronic equipment, preferably in the Semiconductor/MEMS industry
- Familiarity with and ability to use AC/DC multimeters, oscilloscopes, and RF meters is a must
- Must demonstrate knowledge and understanding of basic discrete electronic components and be able to properly troubleshoot them
- Candidate must be able to follow detailed PM procedures and to read circuit layouts
- Must be familiar with basic vacuum, hydraulic and mechanical systems
- Must be familiar with MIOSHA regulations on electrical, mechanical, and chemical safety procedures.
- Must be willing to work extended hours when called for.
To apply please send a resume and references to human_resources@mems-issys.com or fax to 734-547-9964
Sr. Document Control Specialist - Ypsilanti, MI
THIS IS A FULL TIME, TEMPORARY POSITION WITH NO OPPORTUNITY FOR PERMANENT PLACEMENT.
ISSYS is seeking an experienced Medical Device Document Control Professional to assist the Quality Manager with document control management to meet ISO 13485:2003 and U.S. FDA 21 CFR 820 (QSR/cGMP) regulatory requirements. The Sr. Document Control Specialist (SDCS) will coordinate the document change control process for the development of Class II & III medical devices via the engineering change requests, review and approval process.
Experience with preparing SOPs, engineering drawings, test protocols, verification & validation documentation, and other development documents is required. The SDCS will assist the Quality Manager with managing paper and electronic Quality documentation systems and coordinate the review, approval, and distribution of controlled documents to ensure compliance and timely completion to meet established timelines.
Must be detail-oriented and posses strong communication and organizational skills. Must be quality driven with the ability to prioritize and manage multiple tasks/projects to completion. Ability to utilize multiple word-processing, database and engineering drawing applications including MS Office applications and Adobe Acrobat and ProE (or similar).
Required Skills
- A college degree in an engineering or life science related field
- 2-5 years of relevant work experience required
- Knowledge of FDA/ISO Quality Systems and Design Control requirements for medical devices
Desired Skills
- Experience with medical device SDLC process
- CAD software
- Wireless MEMS engineering systems
If you meet the necessary requirements, please forward your resume to lwest@mems-issys.com
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