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Connexion’s mission is to provide "best in class" services to job seekers. We strive to achieve excellence in job placement, staffing, and recruiting services while treating candidates with the professionalism and respect they deserve.
Job Responsibility:
Assemble plastic and metal components into medical devices in accordance with approved manufacturing procedures
Utilize small hand tools (both manual and electric), manual presses, assembly fixtures, calibrated instruments, measurement equipment, microscopes, and test fixtures
Utilize documentation such as Bill of Materials, product flow charts, work orders, check sheets, visual aids, production reports and assembly drawings to assemble product and record results
May perform soldering, fabricating, crimping, mechanical assembly, sealing, ultra-sonic welding, bonding and gluing with adhesives, Epoxy or RTV
Kitting assemblies using a parts list, scanner and inventory software as required
Participates in any routine start up or end of day equipment inspections or verifications
Inspects work throughout the assembly process and communicates any quality or operational issues to appropriate leader
Maintain neat, orderly and clean work area to ensure efficiency and no safety hazards. Participate in safety programs, meetings, and trainings as required. Bring safety concerns to the attention of management
Participate in continuous improvement activities as part of a cross-functional team
Meet all quality, quantity and good manufacturing practices to satisfy customer and Regulatory Affairs requirements. Read and/or understand operating procedures for specific products where training has been completed
Show constant attention to detail, and immediately inform supervisor of anything out of the ordinary, or anything which does not conform to the approved process sheets
Work with Engineers and line leads to resolve issues and correct procedures to ensure quality and efficiency
Maintain Clean Room integrity by using proper attire and adherence to Clean Room environment practices and procedures as applicable
Maintain accurate records/documentation related to quality, work in progress, test results, labor (e.g. timecards), and special projects
Adhere to general safety rules, manufacturing procedures, company policies and procedures, ISO, QSR, and FDA regulations
Requirements:
Minimum of 2 years hands-on experience in a manufacturing environment
Experience with assembly, testing and the documentation of mechanical and electrical devices
Exceptional interpersonal, verbal, and written communication skills are required
Willingness to undertake various tasks and adapt to unexpected situations within dynamic company environment
Good hand eye coordination and manual dexterity required
Small parts assembly and able to work under a microscope
Utilize tweezers, torque drivers, magnifiers and microscopes
Nice to have:
Medical device manufacturing experience preferred
Working knowledge of the medical device regulatory procedures, lean manufacturing, and manufacturing processes preferred