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$24/hr–$30/hr
Full-time
associate degree
Medical Insurance, Dental Insurance, Vision Insurance, Life Insurance, Long Term Disability, 401(k)
Posted 25d ago
~40 hrs/week
Responsibilities
Responsible for testing and evaluating chemical indicators and related products to ensure compliance with performance standards. The role involves operating laboratory equipment, analyzing test data, and maintaining quality records within an FDA and ISO-regulated environment.
Requirements
Requires an Associate's degree in a science-related field or equivalent experience in a regulated medical device manufacturing environment. Candidates must possess strong attention to detail, proficiency in Microsoft Office, and normal color vision.
Full job description
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 quality and continuous improvement. • Additional activities assigned by manager to support quality and production initiatives.
Environmental/Safety/Physical Work Conditions: • Primarily laboratory and office-based environment. • Frequent standing, walking, and sitting. • Regular use of computers and laboratory equipment. • Occasionally lift and/or move up to 20 pounds. • Specific vision requirements include close, distance, depth, peripheral, and color vision. • May be required to work extended hours during peak business periods
Supervision/Management Of Others: N/A
Internal and External Contacts/Relationships:
• Internal: Team members, all Getinge colleagues including the executive and leadership team, Operations, Quality, and R&D teams. Follow up with all levels of management for clarification/approval on reports as needed.
• External: N/A
Disclaimer:
All job requirements are subject to possible modification to reasonably accommodate individuals with disabilities. Some requirements may exclude individuals who pose a direct threat or significant risk to the health and safety of themselves or other employees.
This job description in no way states or implies that these are the only duties to be performed by the employee occupying this position, it is not an exhaustive list of all responsibilities, duties and skills required for the position.
Employees will be required to follow any other job-related instructions and to perform other job-related duties requested by their supervisor in compliance with Federal and State Laws.
Requirements are representative of minimum levels of knowledge, skills and/or abilities. To perform this job successfully, the employee must possess the abilities or aptitudes to perform each duty proficiently. Continued employment remains on an “at-will” basis.
Salary range: $25/hr - $26/hr
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About us
With a firm belief that every person and community should have access to the best possible care, Getinge provides hospitals and life science institutions with products and solutions aiming to improve clinical results and optimize workflows. The offering includes products and solutions for intensive care, cardiovascular procedures, operating rooms, sterile reprocessing and life science. Getinge employs over 12,000 people worldwide and the products are sold in more than 135 countries.
Reasonable accommodations are available upon request for candidates taking part in all aspects of the selection process.
We exist to make life-saving technology accessible to more people.
Industry
Medical Equipment Manufacturing
Company size
10,001+ employees
Headquarters
Gothenburg
LinkedIn followers
350,851
Total funding
$539M
At Getinge, we are committed to meet today's health care challenges together with health care providers and life science professionals and be part of improving patients’ lives around the globe. Our offering includes products and solutions for intensive care, cardiovascular procedures, operating rooms, sterile reprocessing and life science. Our journey started in the village of Getinge on the Swedish west coast back in 1904. Today, our operations cover more than 40 countries, over 12 000 employees, while our products are sold in more than 135 countries. Every single one of us is committed to our purpose to make life-saving solutions accessible for more people.
Please be aware that LinkedIn is a third-party operated social media site unaffiliated with Getinge. Getinge does not control and is not responsible for the privacy or security policies or practices on this site or any third-party websites that we may link to through this site. We recommend that you carefully review the privacy and security practices of this site and any linked third-party websites. We are not responsible for the accuracy of any information, opinions, claims, or statements posted by our followers or other users of this site. Getinge reserves all rights relating to our account on this site, including, but not limited to, removing postings.
While Getinge's product-related advertisement and information is intended to be disseminated only in jurisdictions where the license to market such products has been granted, Getinge has no control over how our posted content is further disseminated through LinkedIn. Therefore, as posts are shared or liked by our followers or other LinkedIn users, we have no control over the geographic reach of such posts, comments, and communications. Please, note the foregoing when reading product-related social media posts and corroborate with local representatives for product licensing.
Offices: Lindholmspiren 7, P.O. Box 8861, Gothenburg, SE-417 56, SE · 40 Continental Blvd, Merrimack, NH 03054, US · Avenida Manuel Bandeira, 291, Bloco B - 2o andar - conjuntos 33 e 34, Sao Paulo, SP 05317-020, BR · 45 Barbour Pond Dr, Wayne, NJ 07470, US · 1 Geoffrey Way, Wayne, New Jersey 07470, US