2027 Spring Co-Op, Development Engineer

Biomet Microfixation, LLC•Jacksonville, FL

3d•Onsite

About The Position

Join Zimmer Biomet's Development Co-Op Program in Jacksonville, Florida. The multi-rotational co-op is aligned with students' cooperative education curriculum. Students perform engineering research and development tasks in a global medical technology organization and contribute innovative solutions to real-world challenges. The program offers technical trainings, certifications, workshops, networking sessions, and day-to-day work experience. Students should be able to complete 3–5 rotations at Zimmer Biomet, including full-time Spring and Fall work assignments, and be willing to temporarily relocate for on-site assignments. Development co-ops generally contribute to the design, development, and processing of orthopedic implants, instruments, and technologies under the direction of a project leader or manager. The role operates in an FDA-regulated environment.

Requirements

Must be actively enrolled in an academic program for the entire duration of the assignment.
Pursuing a B.S. or B.E. degree in an engineering discipline.
Must be available to work full-time (40 hours per week) throughout the co-op session.
Must be authorized to work in the U.S. without requiring employer sponsorship.
Demonstrates excellent technical writing and verbal communication skills.
Ability to work effectively within a team and cross-functionally.
Demonstrates advanced problem-solving skills using quality and statistical tools.
Ability to handle multiple tasks and projects at once.
Must work in an FDA-regulated environment.
Proficiency with Microsoft Office, including Word, Excel, PowerPoint, and Visio.
Able to complete 3–5 rotations, including Spring and Fall full-time work assignments, and willing to temporarily relocate for on-site assignments.

Nice To Haves

Mechanical or Biomedical engineering major preferred.
GPA of 3.2 or higher preferred.
Computer-aided design systems experience is a plus.
GD&T experience is a plus.
Project management skills are a plus.
Product development experience is a plus.

Responsibilities

Generate design control elements, including risk analyses, DFMEAs, and design reviews.
Participate in cross-functional project teams.
Conduct complaint investigations.
Write technical reports.
May participate in cadaveric studies.
Contribute to the design, development, and processing of orthopedic implants, instruments, and technologies under the direction of a project leader or manager.