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Engineering - Non Degreed

Job in Plano, Collin County, Texas, 75086, USA
Listing for: ManpowerGroup Global, Inc.
Full Time position
Listed on 2026-06-18
Job specializations:
  • Manufacturing / Production
    Quality Engineering, Manufacturing Engineer, Medical Device Industry, Electronics Technician
  • Engineering
    Quality Engineering, Manufacturing Engineer, Medical Device Industry, Electronics Technician
Salary/Wage Range or Industry Benchmark: 20 - 23 USD Hourly USD 20.00 23.00 HOUR
Job Description & How to Apply Below
Position: Engineering - Non Degreed I

Title:

Engineering - Non Degreed I

Location:

Plano, TX (100% Onsite)
Duration: 12 months (Possibility of Conversion)
Pay Range: $20/hr to $23/hr (On W2)
Shift Time: 06:00am to 04:30pm

We are looking for a “Engineering - Non Degreed I” to join one of our Fortune 500 clients.

Key Skills
  • Electromechanical assembly
  • Troubleshooting and problem-solving
  • Electrical testing and inspection
  • Use of test equipment (oscilloscope, multimeter, etc.)
  • Attention to detail and documentation accuracy
  • Ability to follow SOPs, drawings, and technical instructions
  • Knowledge of GMP/FDA-regulated environments
  • Computer/data entry skills
Job Responsibilities
  • Set up, calibrate, and operate basic manufacturing equipment in accordance with production schedules and quality standards.
  • Assemble electromechanical subassemblies and finished medical devices, including handling small precision components.
  • Perform functional and electrical testing using automated equipment and manual instruments (oscilloscope, multimeter, function generator).
  • Troubleshoot technical issues related to product lines and manufacturing processes to minimize defects; elevate complex issues as needed.
  • Conduct electrical testing of medical device hardware in compliance with regulatory and quality standards.
  • Support rework, repair, servicing, and refurbishment of nonconforming products.
  • Perform routine and preventive maintenance on production equipment; document activities in CMMS (InforEAM).
  • Maintain accurate production and quality documentation, including Device History Records (DHR), ensuring traceability and compliance.
  • Utilize electronic systems and software tools for data collection and production tracking.
  • Adhere strictly to FDA regulations, Quality Management System (QMS), and Environmental Health & Safety procedures.
  • Support engineering initiatives such as process validation, continuous improvement, and new product introduction (NPI).
  • Identify opportunities to improve manufacturing efficiency, yields, and productivity.
  • Manage priorities across multiple product lines with minimal supervision.
  • Provide cross-functional support and training to team members as needed.
  • Communicate effectively with manufacturing, engineering, and quality teams.
  • Interpret technical documents including SOPs, work instructions, and engineering drawings.
  • Support audits, inspections, and collaborate with internal teams, vendors, and contractors.
Education
  • High school diploma or GED required
  • Technical certification or associate degree in electronics, manufacturing, or related field preferred
  • Typically 0–2 years of relevant manufacturing or production experience (medical device or regulated industry preferred).
Preferred Experience
  • Medical device or highly regulated manufacturing environment
  • Experience with cleanroom operations
  • Familiarity with CMMS systems (InforEAM)
  • Exposure to QMS, EMS, and compliance standards
  • Continuous improvement or lean manufacturing experience.

We are looking for the candidate who are eligible to work with any employers without sponsorship.

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