Mechanical Engineer

Posted 10 Days Ago
Be an Early Applicant
Portsmouth, NH, USA
In-Office
Junior
Healthtech • Biotech
The Role
Supports the product lifecycle and ongoing improvement of medical device product lines. Designs product and component changes, selects materials, develops specifications and packaging, maintains drawings and bills of materials, creates test setups for verification and validation, and prepares production and development documentation in compliance with quality systems and applicable medical device standards.
Summary Generated by Built In

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 PLM Engineering team, the Mechanical Engineer will be responsible for key engineering activities to support ongoing improvements and maintenance of the current product lines in the Laborie Portfolio. This includes aspects including product and component design, material selection, customer and product specification development, packaging design, and other product development activities in support of revenue, quality, production, and cost reduction goals.

 

About the Role:

  • Assist in managing the product life cycle of current product lines in the Laborie portfolio.
  • Design, implement, and deliver product changes to support sales, marketing, production, and service.
  • Maintain and update specifications, material selections, drawings, BOMs, and other design documentation relevant to the product as defined by the quality systems.
  • Work on the development of test setups and systems strategies which will aid in executing design verification/validation studies.
  • Aid in the creation of Production and Development Documentation in compliance with Laborie QMS, ISO, and other applicable standards.

Minimum Qualifications:

  • Bachelor’s degree in mechanical engineering and a minimum of 2 years of engineering design experience.
  • Proficiency in Computer-Aided Design (CAD) software (SolidWorks).
  • Proven experience in the design and development of the product and the change management process.
  • Good understanding and familiarity with engineering concepts including design for excellence, FEA, CTQ design and development, and the engineering change process.
  • Knowledge of applicable standards and regulations such as GMP, FDA’s QSR (CFR 820), IEC 60601 and/or IEC 62304 EU MMD/EU MDR, and ISO 13485, and understanding of test method verification, validation, and analytical methods.

 

Preferred Qualifications:

  • Knowledge of SolidWorks PDM
  • Medical device experience

 

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
  • Awarded 2024 Cigna Healthy Workforce Designation Gold Level

 

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.

 

Skills Required

  • Bachelor’s degree in mechanical engineering
  • At least 2 years of engineering design experience
  • Proficiency with Computer-Aided Design software, specifically SolidWorks
  • Experience designing and developing products and managing engineering changes
  • Understanding of design for excellence, FEA, CTQ design and development, and engineering change processes
  • Knowledge of applicable standards and regulations, including GMP, FDA QSR (21 CFR Part 820), IEC 60601, IEC 62304, EU MDR, and ISO 13485
  • Knowledge of SolidWorks PDM
  • Medical device experience
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The Company
HQ: Portsmouth
612 Employees
Year Founded: 1967

What We Do

Laborie develops innovative medical technologies – including diagnostic equipment and consumable supplies – in the Urology, Gastroenterology, Gynecology, Obstetrics and Neonatology fields. We take great pride in supporting doctors, nurses, hospitals, clinics, academic institutions and patients with treatment and diagnostic innovations. LABORIE is comprised of a variety of powerful brands – cultivated over more than 50 years of providing innovative products and services to our customers. Our story is one of continuous profitable growth, driven both organically and inorganically through mergers and acquisitions. We are privately owned by Patricia Industries and a part of the Investor AB network. Our owners take a long-term investment approach and create value for people and society by building strong and sustainable businesses. We know the work we do at LABORIE matters – we’re making a positive impact in the lives of patients across the globe. This is what fuels our motivation each day.

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