Senior Design Quality Engineer

ZipRecruiter; Falmouth; On-site; GBP 40,000 - 60,000; Full time

Job summary

A leading recruitment platform in Falmouth is looking for a Senior Design Quality Engineer to implement quality management systems and lead design control activities. The ideal candidate will have over 4 years of experience in medical device production, strong leadership skills, and expertise in circuit design. This role is crucial for ensuring compliance with industry standards and enhancing product quality.

Qualifications

• ≥ 4 years of experience in a similar role, preferably medical device production.
• Expertise in analog and digital circuit design and layout.

Responsibilities

• Drive and lead validation processes, testing and verification.
• Supplier engagement, evaluation and interaction.
• Communicate key technical content to stakeholders.

Skills

Quality management systems

Risk management

Cross-functional team leadership

Continuous improvement

Decision making

Education

BSc / BEng in Electronics, Electrical Engineering, Robotics, Mechatronics

Tools

Altium Schematic Capture

Job description

Overview

In the role of Sr. Design Quality Engineer, you will be responsible for implementing and maintaining robust quality management systems, leading DQE deliverables 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.

Your key responsibilities

• Drive and lead validation processes, testing and verification
• Identify and manage risk
• Supplier engagement, evaluation and interaction
• Create and support Continuous improvement
• CAPA/Non-conformance
• Design Reviews and evaluations
• Communicate key technical content to stakeholders

Your Qualifications

• BSc / BEng in Electronics, Electrical Engineering, Robotics, Mechatronics or combination of related fields.
• ≥ 4 years of experience in a similar role, preferably 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