Job description

Acumed LLC As a part of the global industrial organization Marmon Holdings—which is backed by Berkshire Hathaway— you’ll be doing things that matter, leading at every level, and winning a better way. We’re committed to making a positive impact on the world, providing you with diverse learning and working opportunities, and fostering a culture where everyone’s empowered to be their best. Location: Hillsboro, Oregon or Addison, Texas Job Scope The Staff Product Engineer, Tray & Packaging develops, designs, and tests sterile and non-sterile packaging solutions that protect Acumed products during transport, storage, and surgery. This includes customized surgical tray systems supporting product reprocessing/re-sterilization and sterile packaging that maintains sterile barriers throughout the product lifecycle. This role leads technical activities from research and concept development through specifications, testing, validation, and implementation, while supporting existing packaging solutions and continuous improvement efforts. Duties/Responsibilities Leads engineering scope and deliverables for large or complex projects. Provides technical leadership, resolves recurring issues, and establishes design and testing standards. Mentors engineers and staff across projects and technical specialty areas. Manages external vendors and partners with Manufacturing on new technologies and processes. Works with hospital staff, consultants, and field representatives to understand unmet needs and develop solutions. Communicates with and influences internal and external stakeholders, including executives and sales partners. Develops complex test methods and approves test protocols/reports and Engineering Change Requests (ECRs), when delegated. Standardizes testing/design processes and develops internal testing capabilities and equipment. Participates in technical review boards and industry standards activities. Serves as Packaging Engineering liaison to Business Units and supports department KPIs. Qualifications Bachelor’s degree in Mechanical Engineering, Bio-Mechanical Engineering, or equivalent with 8 years of experience preferred; or 14 years of medical device development experience. Experience leading complex projects and mentoring engineers/interns. Highly proficient in medical device packaging design and sterile packaging testing. Highly proficient in testing methods for reprocessing reusable medical devices. Proficient in medical device packaging manufacturing processes and technical writing. Advanced knowledge of Operating Room and Central Sterile management techniques and products. Ability to independently develop technical solutions and intellectual property. Strong communication skills with cross-functional teams, HCPs, executives, and senior management. Ability to develop HCP relationships and independently review multiple projects. Ability to write technical product papers and provide budget input as needed. Following receipt of a conditional offer of employment, candidates will be required to complete additional job-related screening processes as permitted or required by applicable law . We are an equal opportunity employer, and all applicants will be considered for employment without attention to their membership in any protected class. If you require any reasonable accommodation to complete your application or any part of the recruiting process, please email your request to careers marmon.com, and please be sure to include the title and the location of the position for which you are applying.

Requirements

Must-haves

Location: Hillsboro, Oregon or Addison, Texas
Duties/Responsibilities
Leads engineering scope and deliverables for large or complex projects.
Provides technical leadership, resolves recurring issues, and establishes design and testing standards.
Mentors engineers and staff across projects and technical specialty areas.
Manages external vendors and partners with Manufacturing on new technologies and processes.
Works with hospital staff, consultants, and field representatives to understand unmet needs and develop solutions.
Communicates with and influences internal and external stakeholders, including executives and sales partners.
Develops complex test methods and approves test protocols/reports and Engineering Change Requests (ECRs), when delegated.
Standardizes testing/design processes and develops internal testing capabilities and equipment.
Participates in technical review boards and industry standards activities.
Serves as Packaging Engineering liaison to Business Units and supports department KPIs.
Experience leading complex projects and mentoring engineers/interns.
Highly proficient in medical device packaging design and sterile packaging testing.
Highly proficient in testing methods for reprocessing reusable medical devices.
Proficient in medical device packaging manufacturing processes and technical writing.
Advanced knowledge of Operating Room and Central Sterile management techniques and products.
Ability to independently develop technical solutions and intellectual property.
Strong communication skills with cross-functional teams, HCPs, executives, and senior management.
Ability to develop HCP relationships and independently review multiple projects.
Ability to write technical product papers and provide budget input as needed.
Following receipt of a conditional offer of employment, candidates will be required to complete additional job-related screening processes as permitted or required by applicable law .

Nice-to-haves

Bachelor’s degree in Mechanical Engineering, Bio-Mechanical Engineering, or equivalent with 8 years of experience preferred; or 14 years of medical device development experience.

Application prep

Use the role’s language and application details while tailoring your materials.

Platform: workday
Effort: long