Engineering Non Degreed I

Job Title: Test Technician

Work Site: Irving TX 75038 Onsite

Duration: 12 Months Contract with possible extension

Shift/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)

Job Description:

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.

Duties:

• 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.
• 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 Qualifications:

• Experience with electronic assembly and test in a medical device industry preferred.
• High School Diploma or equivalency is required preferred AAS
• 2 or more years experience with electromechanical assemblies/electronic manufacturing technical certifications etc. preferred

Preferred Qualifications:

• 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 environment.
• Strong verbal and written communications with ability to effectively communicate at multiple levels in the organization.