Nesco is seeking a Senior Mechanical R&D Engineer with medical device experience to join our client's team at their Monroe, CT location. Are you excited to create medical products for our wide range of customers, comfortable in a fast-paced environment, and proud that your efforts ultimately lead to improved quality of life for patients? If so, we would love to talk to you.
The Senior Mechanical R&D Engineer is the primary resource on product development or other technical projects. The position is responsible for design, development, testing, troubleshooting, technical documentation, transfer to manufacturing, conformance to all relevant regulations, and, ultimately, meeting project objectives.
RESPONSIBILITIES
- Designs, prototypes, tests and develops components, sub-assemblies, systems and full products.
- Creates test protocols, runs experiments and writes test reports.
- Completes product documentation.
- Analyzes complex engineering problems, defines them, and recommends and implements solutions.
- Leads projects with respect to timelines, budgets, and customer interactions.
- Proficient with mechanical design tools (e.g. SolidWorks), GD&T, Finite Element Analysis, free body diagrams, FMEA, engineering drawings and documentation.
- Proficient with designing and testing using rapid prototyping techniques, as well as designing for common manufacturing approaches.
- Invents, innovates, and launches products.
- Analyzes and solves problems.
- Experience with root cause analysis and corrective/preventive action procedures.
- Experience with lab testing and fabrication equipment (e.g. force gauges & test stands w/data acquisition, 3D printers, etc.)
- Proficient in interacting with all functions within a business.
- Experience in clinical and/or pre-clinical settings a plus.
- Communicates well. Interacts with customers. Effectively presents technical materials to non-technical people.
- Knowledgeable of and works within FDA, MDR, ISO, IEC 60601, and other relevant regulations and standards.
- Bachelor's Degree in Mechanical Engineering or equivalent with 10+ years industry experience, Master's degree with 8+ years industry experience.
- Thorough understanding of medical device manufacturing, especially as it relates to FDA (cGMP) manufacturing requirements.
- Passing a background check, which may include verification of prior employment, criminal conviction, educational and driving records.
- Direct hire with benefits
- 1st shift, Monday – Friday
N esco Resource and affiliates (Lehigh G.I.T Inc, and Callos Resource, LLC) is an equal employment opportunity employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, or veteran status, or any other legally protected characteristics with respect to employment opportunities.