Engineering - Non Degreed I

Job Title: Test TechnicianWork Site: Irving, TX 75038 Onsite Duration: 12 Months Contract with possible extensionShift/Schedule: 1st shift / 6:00am - 2:30pm/ Mon - Fri [5/8](Training Days: 8:45 to 3:30 Monday, 7:00 to 3:30 Tuesday, 6:00am to 2:30 next 8 days)/Range: $$$$/hr on W-2 through Select Source InternationalJob DescriptionWorking under general supervision, this position is responsible for the production of high-quality medical device instruments. This position includes detailed assembly and testing of various electronic components and finished devices in a controlled manufacturing environment.DutiesPerforms testing of electronic components and assemblies using automated test equipment.May perform mechanical assembly of electromechanical subassemblies and devicesAbility to read, comprehend and follow written procedures; understand and follow verbal instructions.Reads and interprets engineering drawings, schematics, and complex test procedures.Participates in continuous improvement/quality initiatives to enhance production processes to achieve quality and profitability metrics.Maintains accurate records to ensure Device History Records and quality documents are accurate, all parts are traceable and quality issues can be addressed to assure the quality of all products.Prioritizes work by determining the sequencing and timing of different jobs based on precedence and importance.Positively represents the company during tours by demonstrating techniques and sharing appropriate information.Minimum QualificationsExperience with electronic assembly and test in a medical device industry preferred.High School Diploma or equivalency is required, preferred AAS2 or more years experience with electromechanical assemblies/electronic manufacturing, technical certifications, etc. preferredPreferred QualificationsExperience in troubleshooting equipment, building and or testing of electronic assembliesWorking knowledge of IPC standards and use of complex tools and equipment specific to functional areasExperience in GMP, ISO, and FDA controlled environments preferredAbility to work within a team and as an individual contributor in a fast-paced, changing environment.Strong verbal and written communications with ability to effectively communicate at multiple levels in the organization.