Engineer, R&D

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    "datePosted": "2026-06-03T04:00:00.000Z",
    "description": "<h2>Overview</h2>\n<p>The R&D engineer will work as a member of a multi-disciplinary team to develop and manufacture medical devices and their production space.  Project scope may include new and next generation products, line extensions, manufacturing technology transfers, and general product improvements.  Seeking an individual who can work with a team on complex tasks including product and process prototyping, testing, data analysis, report writing, and project planning.</p>\n<h2>Responsibilities</h2>\n<p>Research</p>\n<ul>\n <li>Support biologic research including biologic product transfers and new biologic medical devices</li>\n <li>Update and improve current biologic manufacturing processes</li>\n <li>Research into new biological products including literature review, bench studies and early product developement.</li>\n</ul>\n<p>Design & Development</p>\n<ul>\n <li>Develop prototypes, test methods, and production aids using SolidWorks</li>\n <li>Solve complex technical challenges related to product design and manufacturability</li>\n <li>Optimize designs for scalability and cost efficiency</li>\n</ul>\n<p>Validation & Analysis</p>\n<ul>\n <li>Develop and execute validation protocols (IQ/OQ/PQ) and test methods</li>\n <li>Analyze test data using statistical tools to ensure designs meet performance and regulatory requirements</li>\n <li>Document and communicate results through clear technical reports</li>\n</ul>\n<p>Pay range $100,000-$115,000 per year plus bonus. The range provided is based on what we believe is a reasonable estimate for the base pay range for this job at the time of posting. The actual base salary pay will be based on a number of factors such as education, qualifications, certifications, experience, and other job-related factors permitted by law.</p>\n<h2>Qualifications</h2>\n<p>Required</p>\n<ul>\n <li>Bachelor’s degree in Bioengineering, Biomedical Engineering, Mechanical Engineering or related field</li>\n <li>2-3 years of experience in engineering, preferably in medical devices or regulated industries</li>\n <li>Experience with validation (IQ/OQ/PQ) and design controls</li>\n <li>Understanding of statistical analysis and data-driven decision-making</li>\n</ul>\n<p>Preferred</p>\n<ul>\n <li>Proficiency in SolidWorks</li>\n <li>Life Sciences background (cell, tissue, physiology, biochemistry, chemistry, etc.)</li>\n <li>Comfort with handling xenografts and allografts.</li>\n</ul>\n<p>Additional Skills</p>\n<ul>\n <li>Strong problem-solving and critical thinking skills</li>\n <li>Excellent written and verbal communication</li>\n <li>Ability to balance multiple priorities in a fast-paced environment</li>\n <li>Effective collaborator across cross-functional teams</li>\n</ul>\n<p>Additional Information</p>\n<ul>\n <li>Travel up to 15% (including occasional surgical case observation)</li>\n</ul>\n<h2>EEO Statement</h2>\n<p>In order to provide equal employment and advancement opportunities to all individuals, employment decisions at LeMaitre Vascular will be based on merit, qualifications, and abilities. LeMaitre Vascular does not discriminate in employment opportunities or practices on the basis of race, color, religion, sex, national origin, age, disability, sexual orientation, gender identity, breastfeeding or related medical conditions, religious dress, military or veteran status or any other characteristic protected by law. </p>\n<p> </p>\n<p>This policy governs all aspects of employment, including selection, job assignment, compensation, discipline, termination, and access to benefits and training.</p>\n<p> </p>\n<p>Applicants with disabilities may contact LeMaitre HR coordinators via telephone, fax, e-mail, and other means to request and arrange for accommodations. If you need assistance to accommodate a disability, you may request an accommodation at any time. Please contact LeMaitre HR at [email protected].</p>",
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