The Engineering Technician will support the Manufacturing Engineering Team with maintaining the processing of our existing commercially released medical devices. Responsibilities include assisting engineers with daily activities including execution of engineering studies, product testing, process development, training, change orders and Pilot Shop Order (PSO) builds.
Who You Are:
Someone with a strong desire to assist with design control and compliance activities for medical devices and components. This includes working as an individual contributor to support various projects with testing and building of devices for design and process control activities, design changes, test method development, creation of specifications and Design Verification and Design Validation. You have hands on experience in a laboratory or manufacturing environment and have strong analytical, interpersonal, and writing skills (including change control). You possess the ability to thrive in a fast-paced, multidisciplinary environment supporting the team effort to drive project completion and strive to play an active role in company objectives as well as your own personal growth and development.
Flexible work hours and options are available however, the position is expected to have on-site responsibilities performing engineering studies and product testing.
High School Diploma or equivalent is required; an Associate's degree is preferred.
A minimum of three years' experience in the medical device or other regulated industry (or equivalent education experience).
Strong experience with Microsoft Office applications (Word/Excel/PowerPoint) is required.
Required Knowledge, Skills and Abilities
A hands-on individual capable of building device concepts under limited technical supervision.
Able to maintain feasibility/process troubleshooting build information, test results, charts, schematics, and other information in engineering notebooks.
Ability to learn new skills including new software tools and apply acquired skills to improve productivity.
Strong communication skills (verbal/written) and ability to work with a multi-departmental cross-functional team.
This job requires knowledge of medical device regulations including Good Documentation Practices (GDP), Quality Management Systems (QMS) requirements and following Standard Operating Procedures (SOPs/SPs).
Excellent verbal and written communication skills.
Experience with Agile PLM and Minitab desired.
Experience with CAD software (SolidWorks) is a plus.
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.
We look forward to receiving your application. If you share our passion and believe that saving lives is the greatest job in the world, then we look forward to receiving your application. We hope you will join us on our journey to become the world's most desired medtech company.
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