PLM Engineer I

We believe that great healthcare is an essential safeguard of human dignity.

At Laborie, we know the work we do matters - it's what fuels our motivation and contributes to our success. If you're ready to make a positive impact in the lives of patients across the globe, we'd like to meet you.

We support and empower our employees to grow their careers in an environment that encourages a sense of belonging and a connection to doing good. We're not afraid to roll up our sleeves to make our goals a reality and work together to solve for our customers. We reward and recognize our employees based on our values of Aspire to Greatness, Respect All, Own It, Working Together, Persist with Passion.

Who We're Looking For:

As a key member of the R&D team, the Product Lifecycle Management (PLM) Engineer is responsible for providing R&D support to existing products in our portfolio as well as performing engineering activities in support of product acquisitions. This includes a wide variety of responsibilities including design changes, material changes, specification changes, packaging changes etc. in support of revenue, quality, compliance, production, and cost reduction goals. The PLM engineer may also support New Product Development projects and perform design transfer activities.

About the Role:

Responsible for product design ownership for commercialized products. Work closely with supply chain, manufacturing engineering, quality, and regulatory to assess and implement changes that impact the product design.

Develop and advance knowledge of the Design Controls process according to 21 CFR 820 and ISO 13485; perform risk assessments per ISO 14971 and generate/maintain Risk Management Files.

The engineer will be responsible for a variety of activities on new product development, including design, prototyping, material selection, human factors engineering, verification and validation, design for manufacture/manufacturing transfer.

Creates, maintains and remediates specifications, material selections, drawings and other design control documentation relevant to the product as defined by the quality system. Minimum Qualifications:

Requires a minimum of 2 - 4 years of experience and a bachelor's degree in mechanical engineering, Materials Science & Engineering, Biomedical Engineering, or a closely related field. An advanced degree is preferred.

Experience with statistics and design of experiments, project management, and the ability to coordinate cross-functional teams and deliverables.

Technical aptitude, "hands-on" approach to engineering, and good understanding of engineering concepts.

Excellent communication and technical writing skills. Preferred Qualifications:

3D CAD software skills (Solidworks) experience.

Lean / Six Sigma training certifications.

Experience working in a highly regulated industry, such as medical devices or pharmaceuticals, is strongly preferred. Why Laborie:

Our Mission every day is to operate as a world-class specialist medical company making and advancing technologies that preserve and restore human dignity. We do that today by helping people with pelvic and gastrointestinal conditions live normal lives, and by helping mothers and babies have safe deliveries.

Paid time off and paid volunteer time

Medical, Dental, Vision and Flexible Spending Account

Health Savings Account with Company Funded Contributions

401k Retirement Plan with Company Match

Parental Leave and Adoption Services

Health and Wellness Programs and Events

Laborie provides equal employment opportunities and non-discrimination for all employees and qualified applicants without regard to a person's race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation or any characteristic protected under applicable law. Laborie is committed to providing access and reasonable accommodation in our services, activities, education, and employment for individuals with disabilities.