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Quality Documentation Technician

Job in Lenexa, Johnson County, Kansas, 66215, USA
Listing for: TekWissen LLC
Full Time position
Listed on 2026-01-04
Job specializations:
  • Quality Assurance - QA/QC
    Quality Technician/ Inspector, Quality Control / Manager
  • Manufacturing / Production
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 clients 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 :

3 Months

Job Type :

Temporary Assignment

Work Type :

Onsite

Shift :

06 : 00 AM to 06 : 30 PM

Summary :
  • This is a QA Technician position based in Lenexa KS.
  • Responsible for performing in-process and final audits of Device History Records (DHR) to ensure quality compliance and accurate documentation within production areas.
  • This role supports product disposition decisions by verifying adherence to DHR instructions and good documentation practices.
Responsibilities

Conduct in-process audits of DHR records during production

Perform final review of completed DHR records to support product disposition

Ensure quality and regulatory compliance by interacting with production leads and staff to confirm adherence to DHR instructions and good documentation practices

Perform GEMBA observations within operations and follow up to ensure completion of corrective actions

Conduct spot checks of in-process logbooks and related documentation

Support quality assurance compliance for medical device production

Perform additional duties as required to meet quality and operational objectives

Required Skills

Bachelors degree with at least 1 year of quality or production experience in a medical device or pharmaceutical environment

OR

Associate degree with 3 years of relevant experience OR

High school diploma with 5 years of relevant experience

Strong attention to detail

Ability to work independently or as part of a team with minimal supervision

Ability to lift up to 50 pounds

Computer literacy including Microsoft Office and quality / inventory systems

Experience in regulated manufacturing or production environments

Desired Skills

Knowledge of Good Manufacturing Practices (GMP)

Experience with electronic quality systems such as Track Wise

Familiarity with inventory or manufacturing documentation systems

Tek Wissen Group is an equal opportunity employer supporting workforce diversity. a

Key Skills

Quality Assurance,Quality Inspection,Calipers,Coordinate Measuring Machine,Food Industry,GD&T,ISO 9001,Math,Micrometer,Quality Control,HACCP,Manufacturing

Employment Type

:

Full Time

Experience :

years

Vacancy :

1

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