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Engineering - Non Degreed

Job in Irving, Dallas County, Texas, 75084, USA
Listing for: Jobs via Dice
Full Time position
Listed on 2026-03-01
Job specializations:
  • Manufacturing / Production
    Quality Engineering, Electronics Technician, Electronics Assembler, Manufacturing Engineer
  • Engineering
    Quality Engineering, Electronics Technician, Electronics Assembler, Manufacturing Engineer
Salary/Wage Range or Industry Benchmark: 18 USD Hourly USD 18.00 HOUR
Job Description & How to Apply Below

Dice is the leading career destination for tech experts at every stage of their careers. Our client, Generis TEK Inc., is seeking the following.

To discuss this amazing opportunity, reach out to our Talent Acquisition Specialist Smriti Kumari at email address can be reached on #.

Position Details

Engineering - Non Degreed - Irving, TX

Location:

Irving, TX - 75038

Job

Project Duration: 12+ Months Contract

Pay Rate: $18/hr on W2

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
  • 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 continuous improvement/quality initiatives to enhance production processes.
  • Maintains accurate records to ensure Device History Records and quality documents are accurate, all parts are traceable and quality issues can be addressed.
  • 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 QMS, EMS, and other regulatory requirements.
  • Complies with FDA regulations, ISO or other regulatory requirements, Company policies, operating procedures, processes, and task assignments.
  • Adheres to all environmental, health and safety SOPs, equipment, policies and procedures, including any department specific requirements.
  • Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors.
Minimum Qualifications
  • Experience with electronic assembly and test in a medical device industry preferred.
  • High School Diploma or Equivalency 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.
  • 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, stoop, kneel and crouch.
Screening Questions
  • Do you have at least 2 years of experience in electromechanical assembly or electronic manufacturing? Please briefly describe your hands‑on experience with assembly and testing.
  • Have you worked in an FDA, GMP, or ISO‑regulated environment (preferably in medical devices)? If yes, what was your role in maintaining quality documentation or Device History Records?
  • Are you comfortable reading and interpreting engineering drawings, schematics, and using automated test equipment or IPC standards?
  • Are you available to work onsite in Irving, TX for a 12+ month W2 contract at $18/hr, including overtime if required?

To discuss this amazing opportunity, reach out to our Talent Acquisition Specialist Smriti Kumari at email address can be reached on #.

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