- Performs testing of electronic components and assemblies using automated test equipment
- May perform mechanical assembly of electromechanical subassemblies and devices
- Ability to read, comprehend and follow written procedures; understand and follow verbal instructions. May instruct others in the use of all manuals, test procedures and documentation associated with specialized equipment.
- Reads and Interprets engineering drawings, schematics and complex test procedures.
- Participates in continues improvements/quality initiatives in order 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.
- Supports all Company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements.
- Complies with U.S. Food and Drug Administration (FDA) regulations, ISO or other regulatory requirements, Company policies, operating procedures, processes, and task assignments.
- Adheres to all environmental, health and safety SOP's, equipment, policies and procedures, including any department specific requirements.
- Experience with electronic assembly and test in a medical device industry preferred.
- High School Diploma or equivalency is required
- 2 or more years experience with electromechanical assemblies/electronic manufacturing, technical certifications, etc. preferred
- Experience in troubleshooting equipment, building and or testing of electronic assemblies
- Working knowledge of IPC standards and use of complex tools and equipment specific to functional areas
- Experience in GMP, ISO, and FDA controlled environments preferred
- Ability to work within a team and as an individual contributor in a fast-paced, changing enviornment
- Strong verbal and written communications with ability to effectively communicate at multiple levels in the organization
- Multitasks, prioritizes and meets deadlines in timely manner
- Strong organizational and follow-up skills, as well as attention to detail
- Ability to maintain regular and predictable attendance
- Ability to work scheduled overtime as required is preferred
- Ability to hand and lift up to 25 lbs. as needed for specific job functions
- Must be able to sit and/or stand for long periods of time
- Ability to frequently sit, stand, walk, reach with hands and arm's length, stoop, kneel and crouch
- 10 hour shift
- Evening shift
- Irving, TX (Required)
- Irving, TX: Relocate before starting work (Required)
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Engineering - Non Degree 1 (Test Technician) - Irving, United States - NESC Staffing
Description
Job Summary:
Working 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.
Job Responsibilities:
Minimum Qualifications:
Preferred Qualifications:
Job Type:
Full-time
Schedule:
Ability to Commute:
Ability to Relocate:
Work Location:
In person