Design Quality Engineer 2

Smith+Nephew; Coimbra; Híbrido; EUR 35 000 - 45 000; Tempo integral

Resumo da oferta

A leading medical technology company is seeking a Design Quality Engineer 2 in Coimbra to support product development in the Sports Medicine franchise. The role involves ensuring product compliance with medical standards, contributing to manufacturing quality processes, and collaborating across teams. The ideal candidate should have a related bachelor's degree and experience in quality engineering within regulated industries. Benefits include a generous bonus, hybrid work model, and various wellness programs.

Serviços

Generous annual bonus

Flexible vacation and time off

Private health and dental plans

Hybrid working model

Qualificações

• 2-5 years of experience in quality engineering, ideally within the medical device or regulated industry.
• Knowledge of ISO 14971, IEC 62304 and ISO 13485 is preferred.

Responsabilidades

• Support development of new hardware and software products in Sports Medicine.
• Guide projects through design control and risk management.
• Contribute to manufacturing quality processes.

Conhecimentos

Proactive

Detail-oriented

Strong time management

Communication skills

Teamwork skills

Formação académica

Bachelor's degree in engineering or a related technical field

Descrição da oferta de emprego

Life. Unlimited.

At Smith+ Nephew we design and manufacture technology that takes the limits off living.

Join us in Coimbra as a Design Quality Engineer 2 and help shape the future of medical technology. This is your opportunity to grow your career in a collaborative, purpose‑driven environment where innovation meets impact.

What will you be doing?

• You’ll be part of our Quality team, supporting the development of new hardware and software products in the Sports Medicine franchise.
• You’ll work closely with cross‑functional teams to guide projects through design control and risk management, ensuring our products meet the highest standards.
• From design verification and usability testing to regulatory submissions and audit support, you’ll be involved in every step of the product journey.
• You’ll also contribute to manufacturing quality processes and continuously build your expertise in medical device standards and regulations.

What will you need to be successful?

Success in this role means being proactive, detail‑oriented and committed to quality. You’ll bring experience and insight to a team that values collaboration and continuous improvement.

• A bachelor’s degree in engineering or a related technical field
• 2–5 years of experience in quality engineering, ideally within the medical device or regulated industry
• Knowledge of ISO 14971, IEC 62304 and ISO 13485 is preferred
• Strong time management, communication and teamwork skills

We believe in creating the greatest good for society. Our strongest investments are in our people and patients we serve.

Inclusion and Belonging

Committed to welcoming, celebrating and thriving on inclusion and belonging. Learn more about our Employee Inclusion Groups on our website www.smith-nephew.com.

Your Future

Generous annual bonus and pension schemes, Save As You Earn share options.

Work/Life Balance

Flexible vacation and time off, paid holidays and paid volunteering hours, so we can give back to our communities!

Your Wellbeing

Private health and dental plans, healthcare cash plans, income protection, life assurance and much more.

Flexibility

Hybrid working model (for most professional roles).

Training

Hands‑on, team‑customised, mentorship.

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