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QA Technician

Job in Lenexa, Johnson County, Kansas, 66215, USA
Listing for: tsu.edu
Seasonal/Temporary position
Listed on 2026-11-02
Job specializations:
  • Quality Assurance - QA/QC
    Quality Control - QC Analysts/Managers, QA Specialist - Analyst/Manager
Salary/Wage Range or Industry Benchmark: 18 - 26 USD Hourly USD 18.00 26.00 HOUR
Job Description & How to Apply Below
Overview:

Tek Wissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to our clients worldwide. The job opportunity is for one of our clients specializing in biotechnology product development services. Our client is dedicated to supplying laboratory equipment, chemicals, supplies, and services essential in healthcare, scientific research, safety, and education. As the global leader in serving the field of science, our client boasts an annual revenue of around $40 billion with a mission to empower customers to make the world healthier, cleaner, and safer.

Our client's global team is committed to delivering an unparalleled blend of cutting-edge technologies, convenient procurement options, and pharmaceutical services under their industry-leading brands. Position: QA Technician

Location:

Lenexa, KS - 66215 Duration: 6 Months Job Type: Temporary Assignment Work Type:
Onsite Shift: Monday-Friday 08:00 AM to 04:30 PM

Summary

The QA Technician will review batch records, identify documentation errors, and coordinate with Operations to resolve errors or raise issues as part of the quality assessment of products. This person will also be responsible for filing and document retrieval as needed. The QA Technician requires excellent attention to detail, organizational skills and interpersonal skills to ensure timely and accurate evaluation of documentation.

Key Responsibilities
  • Review production batch documentation for compliance with cGMP good documentation requirements.
  • Communicate effectively and coordinate tasks with Manufacturing and Quality Control to facilitate timely release of products.
  • Process 100% inspection rework activities and stock adjustments.
  • Track and trend functional metrics.
  • Support compliance initiatives and Regulatory and Customer Audits.
  • Assist with continuous improvement projects and participate in lean activities.
  • Work requires recurring bending, crouching, stretching, or reaching. Or may frequently operate equipment, including keyboard with mouse and must walk, sit or stand immobile for prolonged periods.
  • Usually in a comfortable environment but does require time on production floor to collect documentation.
Minimum Requirements
  • High School Diploma or equivalent.
  • Working knowledge of various computer software programs such as Teams and Excel.
  • Self Motivated and able to work in a team environment.
  • Able to work in filing room environment and lift 50 lbs for document archival, as needed.
Preferred Requirements
  • 1+ years of experience in QA, QC, or manufacturing within a regulated environment such as medical device, pharmaceutical, or food manufacturing.
  • Background in Medical device, cGMP, or ISO certified environment.
  • Data entry skills and familiarity with inventory management systems such as SAP.
  • Proven ability to work effectively as a member of a cross-functional team.

Tek Wissen Group is an equal opportunity employer supporting workforce diversity

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