Jr. Design Quality Engineer

3 semanas atrás

Coimbra, Portugal Smith+Nephew Tempo inteiro

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

This position will be based in Coimbra (Hybrid role) and will be reporting to Design and Quality Engineering Manager. This role will implement, support, and sustain elements of Smith & Nephew’s Quality System through procedure generation, training, auditing, and technical support. The Quality Engineer determines methods, techniques, and evaluation criteria for medical devices. He/she serves as a key resource for ISO, EN, MDR, and QSR requirements.

What will you be doing?

Provide quality leadership to product support project teams as the quality engineering representative. Work with a team to develop methods and procedures to ensure that the appropriate tests are conducted to assure that products meet the required specifications/standards and that the safety and reliability of products are established. Generate/approve/manage design verifications, design validations, sterilization validations, process validations, supplier qualifications, test methods, capability studies, and risk management documentation.

Support manufacturing operations and provide expertise in product requirements, risk management, test methods, and statistical analysis.

Ensure compliance to product specific standards, cGMP, QSR, US FDA, ISO, IEC, UL, EN, and MDD/EU MDR requirements. Ensure that all the responsibilities within the scope of this job comply with the scope of the Quality System.

Work with outside labs and suppliers to communicate Smith & Nephew product / process requirements as well as assess capabilities of the outside lab / supplier.

Support continuous improvement activities (CCRs and/or PARs).

Support Post Market Surveillance activities, Management Review, and audits/inspections.

What will you need to be successful?

Education: Bachelor’s degree in engineering or related discipline

Experience: No experience required -Some medical device or related regulated industry or internship will be valuable.

Fluent spoken and written in English.

Competences:

Need to be able to make sound decisions with attention to details

Understanding the impact of regulatory requirements (eg. GMP’s, ISO 13485, ISO 14971, and MDR) on Smith & Nephew’s products is necessary

Must be able to provide and implement solutions to quality problems

Ability to plan and schedule multiple projects and tasks

Effective written/oral communication skills

Team player

MS Office, MS Excel, and Statistical software proficiency

You. Unlimited.

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

Inclusion, Diversity and Equity: Committed to Welcoming, Celebrating and Thriving on Diversity, Learn more about our Employee Inclusion Groups on our website () Your Future: Generous annual bonus, Save As You Earn share options. Work/Life Balance: Meal allowance, School Allowance, Flexible Vacation and Time Off, Paid Holidays and Paid Volunteering Hours, so we can give back to our communities Flexibility: Hybrid Working Model (For most professional roles). Training: Hands-On, Team-Customised, Mentorship.

Applications:

If you share our passion for pioneering innovation and can demonstrate how you meet the criteria outlined, we would love to hear from you.

We continue to actively build an environment where every individual can fulfil their potential and be proud ambassadors for Smith & Nephew, our customers and their patients.

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