Job Summary: We are seeking a highly skilled and motivated Mechanical Engineer to join our team in the medical device space. The ideal candidate will have strong experience in mechanical testing and prototyping, with a focus on developing innovative medical devices. This role involves collaboration with cross-functional teams to design, test, and refine medical devices that meet regulatory standards and improve patient outcomes.Key Responsibilities:Mechanical Testing: Conduct mechanical testing of medical devices to ensure they meet performance and safety standards. This includes designing and executing test protocols, analyzing test data, and documenting results.Prototyping: Develop and refine prototypes of medical devices using CAD software and 3D printing technologies. Collaborate with design and manufacturing teams to iterate on designs and improve functionality.Design and Development: Work closely with R&D scientists and engineers to assist in the preparation and testing of various concepts. Assist in the creation of design drawings and specifications for new products.Documentation: Maintain detailed documentation of development studies, including analysis, authoring protocols, and reports. Ensure all documentation complies with regulatory requirements.Collaboration: Collaborate with cross-functional teams, including marketing, IT, and customer service, to ensure the successful development and launch of medical devices.Troubleshooting: Identify and resolve issues with prototypes and production devices. Perform root cause analysis and implement corrective actions to improve product reliability.Regulatory Compliance: Ensure all designs and processes comply with relevant regulatory standards, including ISO 13485 and FDA guidelines.Qualifications:Bachelor's degree in Mechanical Engineering or a related field.Proficiency in CAD software (e.g., SolidWorks, Creo) and 3D printing technologies.Strong understanding of mechanical testing methodologies and data analysis.Excellent problem-solving skills and attention to detail.Ability to work independently and as part of a team.Strong communication skills, both written and verbal.Knowledge of regulatory standards for medical devices (ISO 13485, FDA guidelines) is a plus.About ActalentActalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.Diversity, Equity & InclusionAt Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:Hiring diverse talentMaintaining an inclusive environment through persistent self-reflectionBuilding a culture of care, engagement, and recognition with clear outcomesEnsuring growth opportunities for our peopleThe company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email (% ) for other accommodation options.