Senior Design Quality Engineer
About The Position
At CooperSurgical (CSI) we are currently looking to recruit a Sr. Design Quality Engineer to our team in Falmouth UK. You will be part of a team of experienced R&D engineers leading, designing and testing our medical device products developed on site and across the Global R&D team. In this role you will be responsible for ensuring the safety, effectiveness, and compliance of our medical devices throughout the design and development lifecycle. The role reports directly to the Manager of Design Engineering. Applicants must be eligible to work in UK and be on-site at Falmouth, Cornwall UK. In the role of Sr. Design Quality Engineer, you will be responsible for implementing and maintaining robust quality management systems, leading DQE deliverable to support design control activities, and collaborating with internal and external cross-functional teams to deliver cutting-edge medical solutions. This individual will be expected to apply his/her knowledge of design control principles and quality engineering techniques to positively influence development efforts as needed. In parallel, this person shall also ensure the products are developed and manufactured in accordance with applicable industry standards, regulatory requirements, and customer requirements. Review and evaluate scientific and technical data as it pertains to product and product testing and lead teams to identify and solve complex product problems. This position also coaches, reviews and delegates work to lower level specialists. You thrive in a dynamic and challenging environment. You will work closely with teammates and stakeholders in the wider organization. The position of Sr. Design Quality Engineer is vital for the success and growth of the CooperSurgical company.
Requirements
- BSc / BEng in Electronics, Electrical Engineering, Robotics, Mechatronics or combination of related fields.
- ≥ 4 years of experience from a similar role, - preferable medical device production
- Expertise in analog and digital circuit design and layout using tools like Altium Schematic Capture.
- Demonstrated skills in decision making preferably across a broad spectrum of Quality Engineering responsibilities
- Proven experience leading cross-functional teams in a medical device development environment
- Strong interpersonal, organizational and project management skills
- Experience with Design for Manufacturing and Assembly (DFMA)
- Fluent English (spoken and written) is mandatory
Responsibilities
- Drive and lead validation processes, testing and Verification
- Identify and manage risk
- Supplier engagement, evaluation and interaction
- Create and support Continues improvement
- CAPA/Non- conformance
- Design Reviews and evaluations
- Communicate key technical content to stakeholders
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What This Job Offers
Job Type
Full-time
Career Level
Senior
Industry
Miscellaneous Manufacturing
Number of Employees
5,001-10,000 employees
