Design Engineer II
Job Summary
This Engineer is a skilled professional responsible for contributing to engineering projects and collaborating with cross-functional teams to design develop and implement solutions. You will play an essential role in ensuring the successful execution of engineering tasks and projects to tight time scales and ensuring functional and non-functional requirements are met. This opportunity to be a part ofresearch and development workstreams subsystems and/or specific products and deliverables in the domains ranging from simple disposable devices to complex thermos-fluidic system and sophisticated robotic solutions involving IT connectivity machine learning and AI.
As an R&D engineer you will be a part of the product development and engineering department you will report directly to the R&D Director Product Engineering. Scope of this role includes activities pertaining to sustaining activities new product development product upgrades and improvements line extensions as well as new concept incubation activities. Within the scope of this role are electro-mechanical connected systems and devices associated with In-vitro fertilization (IVF) and Assisted Reproductive Technologies (ART). You will also have an opportunity to contribute to product development and sustaining engineering activities associate with surgical devices instruments and disposables in broader womens health field including Obstetrics and Gynecology (OBGYN). In this role withinthe Global Cooper Surgical R&D organization and you may as needs arise be asked to support other areas of the business to ensure the success of the company in line with the One Cooper philosophy.
Responsibilities
Technical Contributions:
Design and develop components and assemblies using first principles Lead development of product or sub-systems for complex electromechanical products and analyze / simulate design to understand key parameters and sensitivities. Establish design feasibility by testing circuit and demonstrating statistical capability for critical functions.
Define design inputs (i.e. product requirements) develop design outputs (i.e. product specifications) define technical strategies for an adequate verification and validation approach. Drive successful verification and validation testing.
Ideate conceptualize and build concepts and prototypes to aid incubation of new opportunities or down-select wining solutions for new product developments upgrades or improvements.
Create simulation and mathematical models as appropriate to demonstrate functional feasibility of technical solution based on experimental numerical statistical and/or finite-elements tools and techniques.
Participate in troubleshooting root-cause analysis and devise solutions and approaches for solving technical problems (solution gameplan) and overcoming development challenges in an inclusive and collaborative fashion.
Develop test methods and fixtures for products components and systems simulation evaluation and verification testing including creating formal Verification test protocols run tests and write Verification test reports.
May communicate key technical content to parties within and outside of own function (R&D). May have responsibility for communicating with parties external to the organization and manage external development partners to meet project deliverables on time.
Project Delivering:
Deliver agreed project outcomes on-time and on-budget per project plan.
Participate in design review and DFMA activities.
ORGANIZATIONAL AND PROCESS EFFECTIVENESS
Aid in the effective cross-functional collaboration ensuring timely and efficient delivery of target business outcomes.
Contribute to the assessment of new opportunities acquisition targets competitive products and Intellectual Properties (IPs) to aid competitiveness and differentiation of our business offerings.
Support scoping project planning and product requirement definition for new product development upgrades or line extensions as appropriate.
Contribute to the selection evaluation and implementation of new tools techniques and best practices to ensure state-of-the-art product development capabilities and best practices.
SAFETY EFFICACY AND COMPLIANCE
Ensure adherence to medical devices design control compliance by ensuring all applicable safety quality and regulatory guidelines and policies are followed to develop safe and effective products.
Maintain technical documentation for project and products as applicable per company quality standards policies and procedures and well as engineering best practices and functional excellence requirements.
Qualifications
MEng or BEng (Hons) Degree or equivalent.
Highly Proficient in engineering designs and creation of engineering drawings required.
Medical device development experience with thorough understanding of design control guidelines including verification and validation methods required.
Proficiency with engineering first principles and analytical methods including simulation modeling.
Understanding of Design for Manufacturing and Assembly (DFMA) required.
Understanding of statistical methods including design of experiments required.
Hands-on craft skills and experience with building fixing servicing and/or fabricating concepts fixtures prototypes or similar required.
- Experience with FEA and/or simulation mathematical modeling preferred.
Experience with translating customer to product requirements conducting harm-based risk analysis and defining acceptance criteria preferred.
Experience with electro-mechanical robotic or digital systems preferred.
Experience with Design for Six Sigma (DFSS) preferred.
Experience in drafting testing protocols and reports. - required.
Experience with identifying latent user needs and front-end of innovation process preferred.
Required Experience:
IC
Key Skills
About Company
Live Brightly. Our daily and monthly soft contact lenses are designed with your health and comfort in mind. For every eye, every person, and every day.