Principal Engineer - Quality Process Validation - Defined Term - 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, 401(k) as well as company-paid holidays) all effective first day of employment!

This is a Fixed Term assignement that is slated to run through December 2026.

The Principal Engineer - Quality Process Validation position is an on-site, full-time position. Hours are Monday - Friday, 8 : 00am - 4 : 30pm (with some flexibility).

Job Function Summary :

Assists with current processes, and development of new processes in support of R&D, Manufacturing and Product Development. Provides support and guidance on validation activities related to manufacturing / test equipment and processes.

Job Functions :

• Works to improve efficiency and effectiveness of manufacturing and other facility processes.
• Provides Process Design Engineering guidance to R&D, Manufacturing and Product Development.
• Develop manufacturing processes; process flow documentation and design including process steps, workflow and material handling techniques.
• Assists with applying statistical analysis techniques and lean manufacturing principles to drive operational efficiencies
• Develop new manufacturing methods and procedures.
• Provides input to new equipment designs with emphasis on concurrent engineering and improved productivity techniques.
• Assists with process documentation generation and maintenance.
• Participates in new equipment qualification and validation, and revalidation
• Participates in process and test method qualification and validation.
• Contributes to team effort by accomplishing related duties as requested.
• Update and develop new SOPs.
• Reduce process risks and increase manufacturing process efficiency.
• Quality and Engineering Project work as assigned.

Required Knowledge, Skills and Abilities :

Minimum Requirements :

Quality Requirements :

Environmental / Safety / Physical Work Condition s :

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Supervision / Management Of Others : N / A

Internal and External Contacts / Relationships :

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.

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Salary Range : $160k-$170k annually

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.