IQA Technician I at Experis

Wayne State University; Irving (TX); On-site; USD 25,000 - 30,000; Full time

Job summary

Abbott in Irving, TX is seeking a quality inspection intern for a 6-month, 100% onsite assignment. You will support receiving and inspection of components for medical device assemblies, perform dimensional checks, and ensure compliance with GMP/GLP and QS requirements.

The role emphasizes documentation and data-driven quality improvements. Intern will gain exposure to QS, GMP/GLP controls, and regulatory standards while handling routine inspections under supervision, with potential for more

Qualifications

• Experience with hand measurement tools and procedures.
• Familiar with GMP/GLP and quality system regulations.
• Strong documentation and record-keeping skills.
• Ability to analyze inspection data and identify trends.
• Attention to detail and accuracy.
• Ability to follow standards and regulatory guidelines.
• Basic problem solving and initiative.

Responsibilities

• Support GMP/GLP compliant receiving and inspection activities.
• Operate hand tools and perform visual/dimensional inspections.
• Maintain inspection records and documentation to GMP/QS standards.
• Review drawings/inspection plans and report non-conformances.
• Assist in data collection, trending and process improvements.
• Adhere to FDA/ISO environmental and safety requirements.

Skills

Visual inspection

GMP/GLP knowledge

Documentation

Data analysis

Attention to detail

Regulatory compliance

Problem solving

Education

Bachelor's or technical diploma

Tools

Calipers

Gauges

Rulers

Job description

Location: Irving, TX

Duration: 6 Months

Shifts: 8AM TO 4:30PM

100% Onsite

Duties & Key Responsibilities

• Support manufacturing and testing operations in compliance with Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP) for receiving and inspection.
• Perform job duties in accordance with Abbott Global and Technical Standards and Quality System (QS) requirements.
• Complete Tier 1 inspections per inspection plans and drawings to support production schedules.
• Use hand tools (calipers, gauges, rulers) and perform visual inspections on inbound materials for medical device assembly.
• May operate more advanced measuring instruments as needed.
• Perform visual and dimensional inspections of cable harness assemblies and printed circuit board assemblies.
• Maintain accurate inspection records, documentation, and filing systems to meet GMP and quality compliance.
• Accept or reject supplier lots based on inspection results.
• Document any non conformances related to specifications, procedures, or standards, including completing required paperwork and system transactions.
• Initiate discrepant material reports and participate in data collection, analysis, and trending.
• Recommend improvements to policies, processes, and procedures.
• Perform moderately complex assignments, applying established methods to recurring situations; elevate more complex issues to senior quality personnel.
• Support Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory initiatives.
• Ensure adherence to all FDA, ISO, environmental, health, and safety requirements.

Key Skills

• Ability to perform accurate visual and dimensional inspections.
• Knowledge of GMP, GLP, and quality system regulations.
• Strong documentation and record keeping skills.
• Ability to analyze inspection data and identify trends.
• Attention to detail and accuracy.
• Ability to follow standards, procedures, and regulatory guidelines.
• Basic problem solving and initiative to complete tasks independently.

Required Experience

• Experience with hand measurement tools such as calipers, gauges, and rulers.
• Work experience supporting manufacturing or quality environments preferred.
• Intern will be considered

Preferred Experience (Nice to Have)

• Bachelor’s degree or technical diploma (not required but preferred if no prior inspection experience).
• Familiarity with medical device manufacturing or regulated environments.
• Experience reviewing engineering drawings, specifications, and inspection plans (required)