Senior Quality Engineer

Qualcomm; Munster; On-site; EUR 40,000 - 55,000; Full time

Job summary

A global technology leader is seeking a Quality Assurance Specialist for an 18-month contract in Munster, Ireland. In this role, you will oversee product and process quality, collaborate with suppliers, and manage non-conformances. The ideal candidate should have a Bachelor’s degree in a related field and at least 2 years of QA experience. This position offers comprehensive benefits and a chance to impact healthcare positively.

Benefits

Full Stryker benefits

Qualifications

• Minimum of 2 years’ experience in quality assurance or related field.
• Strong collaboration skills with cross-functional teams.
• Ability to communicate effectively with suppliers.

Responsibilities

• Ensure quality performance of product and processes.
• Manage non-conformances and facilitate closure.
• Support manufacturing process improvements.

Skills

Quality assurance techniques

Risk management practices

Human factor identification

Education

Level 8- BSc in a science, engineering or related discipline

Job description

This is an 18 month contract with full Stryker benefits.

What You'll Do:

Work closely with operations and the business functions to ensure quality performance of product and processes.

Collaborates with Divisional QA, cross-functional and suppliers’ teams to address top quality issues.

Own identified internal and supplier driven non-conformances and manage the timely closure of NC's within Trackwise. Own or support identified CAPAs and manage to timely root cause investigation, implementation and closure.

Disposition non-conforming product within MRB, issuing NC's as appropriate.

Communicate & collaborate with suppliers regarding non-conformances, escalating supplier corrective action requests as required.

Engage in the development and improvement of the internal manufacturing processes for existing products.

Performs critical assessment of internal and supplier proposed change management activities.

Performs PPAP activities for supplier changes

Participates and may lead in the creation and/or review of new or modified procedures.

Maintain KPIs for monitoring of process and/or product quality, perform analysis, and interpret trends, identifying and activating on appropriate actions as necessary.

Support execution and analysis of manufacturing related complaints and product field actions.

Support and Drive Human Factor practices, familiarity in the science of Human Factor identification, reduction, and mitigation.

Collaborate with appropriate stakeholders to identify and execute opportunities for supplier part certification.

Develop understanding of risk management practices and concepts and applies knowledge to manufacturing operations.

What You'll Need:

Level 8- BSc in a science, engineering or related discipline.

Minimum of 2 years’ experience preferred.

Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.

Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer – M/F/Veteran/Disability.