Intern, Manufacturing Engineering Management

Make a meaningful difference to patients around the world. Our University Programs are designed to help early-career professionals contribute to solutions that transform patient lives. We also believe in investing in the future of our talented people across the globe, including early career professionals seeking to explore and establish themselves within the medical device industry. We'll provide you with the opportunity to thrive in a dynamic environment where you can make innovative contributions. As an intern with us, you'll find motivation and inspiration in a culture that emphasizes passion for patients as you discover your own strengths.

How you will make an impact:

. Support equipment testing

. Assist in validation protocol execution for new tools, fixtures and processes e.g. TFIQ

. Document and track process improvement

. Draft IOPQ and software protocols for Tissue Processing and Component (e.g. new transfer projects) equipment

What you'll need (Required):

. Pursuing degree in Biomedical Engineering, Mechanical Engineering, Bioengineering etc. Preferred and

. Course competition of engineering mechanics and mechanical design is preferred.

What else we look for (Preferred):

. Comfortable working in cleanroom environment. Hands-on and highly motivated. Able to follow procedures, perform testing and clearly convey data results.

. Strong interest in pursuing relevant industry experience. Interest in the healthcare and medical devices industry is a plus.

. Attention to detail.

. Be proficient in drafting software (Solidworks or Creo Parametric preferred).

. Must be in good scholastic standing (3.0+ GPA or equivalent).

. Conceptualize, develop, and iterate designs in response to design requirements specified.

. Test new designs (functional testing, mechanical testing, and simulated use) and brainstorm novel ideas for device improvements using test results.

. Assist in documenting production department concerns and aid in troubleshooting and resolving technical problems.

. Provide documentation support and complete written reports on testing and designs.

. Actively participate in design reviews and provide relevant feedback for teammates.

. Adhere to all company rules and requirements (e.g., pandemic protocols, Environmental Health & Safety rules) and take adequate control measures in preventing injuries to themselves and others as well as to the protection of environment and prevention of pollution under their span of influence/control.