QA Lab Technician - Englewood, CO

Getinge•Arvada, CO

4d•$24 - $30•Onsite

About The Position

The QA Laboratory Technician position is an on-site, full-time, non-exempt position. Hours are Monday – Friday, 8:00am – 4:30pm (with some flexibility). This role is responsible for testing and evaluating chemical indicators and related products to ensure compliance with established specifications and performance standards. The technician will operate sterilization and laboratory equipment, analyze test data, maintain accurate records, and support quality assurance activities within an FDA- and ISO-regulated environment.

Requirements

Proficiency in Microsoft Word, Excel, and Outlook.
Strong attention to detail, organization, and data accuracy.
Effective problem-solving and decision-making skills.
Ability to work independently and collaboratively.
Strong written and verbal communication skills.
Ability to manage multiple priorities and meet deadlines.
Normal color vision required
Builds and maintains positive working relationships with colleagues across Operations, Quality, R&D, and other functional areas.
Demonstrates professionalism, teamwork, and a customer-focused mindset.
Communicates clearly and effectively, both verbally and in writing.
Accepts feedback constructively and adapts to changing priorities.
Exhibits reliability, accountability, and a strong commitment to quality and compliance.
Contributes to a collaborative, respectful, and continuous improvement culture.

Nice To Haves

Associate's degree in a science-related field preferred; or a combination of education, training, and relevant experience in a laboratory, quality, or regulated medical device manufacturing environment.
Familiarity with FDA and ISO-regulated environments preferred.

Responsibilities

Conduct in-process and final product performance testing of Steritec Products.
Operate sterilization and laboratory equipment and other inspection equipment according to approved procedures.
Accurately document test results and maintain quality records using good documentation practices.
Manage product retains, control samples, and test samples.
Verify product labels, lot information, and indicator graphics for accuracy.
Collect, analyze, and record data for shelf-life studies and other quality programs.
Complete Performance Releases and Finished Goods Releases for WIP and completed product.
Review Device History Records for accuracy and precision.
Perform Quality Testing and Inspections for incoming and production areas as assigned.
Support additional quality assurance activities as assigned.
Adhere to all applicable FDA, ISO, Quality, and Regulatory requirements.
Complete required Quality and Compliance training.
Follow established procedures and report quality or compliance concerns promptly.
Support and promote a culture of quality and continuous improvement.
Additional activities assigned by manager to support quality and production initiatives.