Quality Documentation Technician
Listed on 2026-01-04
-
Quality Assurance - QA/QC
Quality Technician/ Inspector, Quality Control / Manager -
Manufacturing / Production
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.
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.
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 SkillsBachelors 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 SkillsKnowledge 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 SkillsQuality 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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