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.

Job Overview

The Intern will support the development, optimization, and documentation of manufacturing processes used in the production of medical devices. This role provides hands-on experience in a regulated environment (FDA/QSR, ISO 13485) and offers the opportunity to work alongside experienced engineers to improve product quality, reduce waste, and enhance manufacturing efficiency. The intern will contribute to ongoing projects, assist in testing and validation, and help resolve day-to-day production issues.

Job Responsibilities and Essential Duties

• Assist process engineers with the development, characterization, and improvement of manufacturing processes for medical devices.
• Data collection and Statistical analysis activities to support feasibility studies, parameter development and process optimization.
• Work in a controlled manufacturing environment to monitor/evaluate processes and equipment.
• Support equipment qualifications installation/troubleshooting and fixture development using CAD software (Solidworks)
• Perform testing, measurements, and sample preparation to support engineering studies and validation protocols.
• Maintain a safe and compliant work environment by following all company, regulatory, and quality system requirements.

Minimum Requirements

• Currently pursuing a Bachelor’s degree in Mechanical Engineering, Biomedical Engineering, Packaging Engineering or a related technical field.
• Experience with CAD design with Solidworks, AutoCAD, or similar software required
• Previous experience with design for medical devices a plus
• Lab testing experience a plus
• Knoweldge of FDA regulations a plus 
• Basic understanding of manufacturing processes, engineering principles, and laboratory/test methods.
• Proficiency in Microsoft Office applications (Excel, Word, PowerPoint).
• Strong verbal and written communication skills.

Required Knowledge, Skills and Abilities

• Ability to collect and interpret data using Excel, statistical tools, or basic engineering software.
• Skill in documenting procedures, test results, and engineering findings clearly and accurately.
• Mechanical aptitude and comfort working with tools, fixtures, small components, or test equipment.
• Ability to work collaboratively in a team setting and communicate effectively with engineers, technicians, and operators.
• Strong problem‑solving ability with an analytical mindset and attention to detail.
• Ability to manage multiple tasks, prioritize effectively, and meet deadlines.
• Willingness to learn new processes, equipment, and regulatory expectations within the medical device industry.

Salary Range:  $21 - $23 per hour

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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.  

Getinge is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, pregnancy, genetic information, national origin, disability, protected veteran status or any other characteristic protected by law. Reasonable accommodations are available upon request for candidates taking part in all aspects of the selection process.   

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