QA Lab Technician - Englewood, CO

 

 

With a passion for life

 

Join our diverse teams of passionate people and a career that allows you to develop both personally and professionally. At Getinge we exist to make life-saving technology accessible for more people. To make a true difference for our customers – and to save more lives, we need team players, forward thinkers, and game changers. 

Are you looking for an inspiring career? You just found it.

 

Steritec Products Inc., a member of the Getinge Group, manufactures sterilization and cleaning medical device consumables using ink technology. We manufacture and print highly specialized proprietary inks that undergo specific color changes when exposed to different sterilization conditions in hospital and industrial/pharmaceutical sterilizers.
 
We are located in the beautiful Inverness Business Park in Englewood, CO. We offer a generous benefit package (medical, dental, vision, life, LTD, 401(k) as well as PTO, company-paid holidays and much more) all effective first day of employment!

 

This QA Laboratory Technician position is an on-site, full-time, non-exempt position. Hours are Monday – Friday, 8:00am – 4:30pm (with some flexibility). 

 

Job Function Summary:

Responsible for testing and evaluating chemical indicators and related products to ensure compliance with established specifications and performance standards. Operates sterilization and laboratory equipment, analyzes test data, maintains accurate records, and supports quality assurance activities within an FDA- and ISO-regulated environment.

 

Job Functions:
•    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.

 

Required Knowledge, Skills and Abilities:
•    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

 

Interpersonal & Professional Skills
•    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.

 

Minimum Requirements:
•    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.

 

Quality Requirements
•    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 qu