Senior Quality Engineer

Stryker; Belfast City District; Presencial; GBP 37.000 - 61.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Comprehensive benefits package

Descripción de la vacante

Stryker Corporation in the United Kingdom is seeking a Senior Engineer, Quality Assurance for a fixed-term contract until 31 August 2028. Based onsite in Belfast, you will establish, improve, and maintain the quality system, providing quality engineering support across operations and business functions.

You will drive CAPA, NCR closures, change control, risk management, audits, and continuous improvement initiatives while collaborating with internal and external teams to ensure compliant,

Formación

• 2+ years’ experience in a Quality or Regulatory Affairs role; prior industry experience desirable.
• Proficient understanding of Med Device manufacturing, ISO 13485, GMP.
• Excellent communication skills with attention to detail.
• Strong knowledge of Risk Management, CAPA, Audits and Statistics.
• Fluent in written and spoken English; able to operate in a multi-site team.

Responsabilidades

• Collaborate with operations to ensure quality performance of products and processes.
• Manage internal and supplier NCs, ensuring timely investigation and closure.
• Own CAPAs through root cause analysis to closure.
• Review change management activities and drive effectiveness.
• Support audits and field actions with QA input.
• Lead Lean initiatives to standardize and remove waste.

Conocimientos

Quality Assurance

CAPA/NCR

Root Cause Analysis

Lean Six Sigma

GMP ISO13485

Communication skills

Risk Management

Educación

Honours Bachelor’s Degree

EU EQF Level 6

QA/Regulatory experience

Lean Six Sigma training

Herramientas

Microsoft Word

Microsoft Excel

PowerPoint

MSA methods

Regulatory databases

Descripción del empleo

Work Flexibility: Onsite This is a fixed term contract (inc full benefits) that will run until 31st August 2028.

Position Summary: The Senior Engineer, Quality Assurance will establish, improve and maintain the quality system by providing quality engineering support within operations and other business functions. Advocate and lead the execution of initiatives & projects to enhance quality performance within the business. Ensure to deliver high quality products that meet customer needs. Ensure compliance with regulations and standards.

Essential Duties & Responsibilities:

• Work closely with operations and the business functions to ensure quality performance of product and processes
• Collaborate cross-functionally with internal and external teams to resolve quality issues
• Manages internal and supplier-driven Non-Conformances (NCs), ensuring timely investigation and closure
• Owns Corrective and Preventive Actions (CAPAs) through root cause analysis to closure
• Disposition of non-conforming product through MRB, issuing NCs as appropriate
• Initiates and leads in the development and improvement of the manufacturing processes for existing and new products.
• Review and approval of change management activities, challenges change effectiveness and drives strong review.
• Interpret KPI trends, act as necessary, driving a continuous improvement process.
• Support the execution and analysis of manufacturing complaints and product field actions
• Provide QA support during internal and external audits
• Advocate of Human Factor practices, proficient in the science of Human Factor identification and mitigation.
• Proficient in risk management practices and concepts and applies knowledge to manufacturing operations and identify opportunities and weaknesses
• Lead and participate in the Lean philosophy – standardization and elimination of waste
• Understanding of Human Error Prevention and the application of those principles to the manufacturing environment.
• Support process/equipment validation, qualification, and Measurement System Analysis (MSA)
• Support with product holds and executing containment Plans
• Manage supplier relationships, including but not limited to, coordinating communications, monitoring performance, managing in house and external nonconformities and ensuring timely delivery of quality materials and services.

Education & Special Trainings:

• Honours Bachelor’s Degree – United States of America & Ireland & China
• EQF Level 6 or equivalent– EU
• 2+ years’ experience in a Quality or Regulatory Affairs role; prior industry experiences desirable
• Proficient in understanding of Med Device manufacturing processes, ISO 13485, GMP.
• Lean Six Sigma training is a distinct advantage.
• Excellent communication skills and attention to detail.
• Proficient understanding of engineering and quality principles, including Risk Management, CAPA, Audits, and Statistics
• High level knowledge/experience of Risk Based and statistical techniques, in particular process risk, statistical sampling plans, Process Capability, Gauge R&Rs.
• High level of PC skills. Must be proficient with Microsoft Word, Microsoft Excel and PowerPoint packages.
• Experience in interacting with regulatory agencies (FDA, MoH, TUV, etc.) desired.
• Strong knowledge of Quality Concepts (e.g. Risk Management, CAPA, Audits, Statistics).
• Exhibits strong leadership and mentoring behaviors.
• Strong problem-solving, analytical, and communication skills with high attention to detail
• Builds strong relationships through open communication, respect, and trust
• Team player with a customer/stakeholder-focused approach
• Diplomatic, tactful, and effective at leveraging interpersonal skills
• Embraces change with a continuous improvement mindset.
• Fluent in written and oral English - B2 Level (writing documents, meeting minutes, conference calls, technical writing, presenting etc.)
• Confident representing Quality in cross-functional settings
• Self-starter able to manage multiple tasks in a fast-paced environment
• Willing to work as part of a multi-site team; some travel required United Kingdom

Pay Ranges:

United Kingdom: £36,800 - £61,200 GBP Annual At Stryker, we believe transparency helps candidates make confident decisions about their next career step. Compensation is an important part of that process and we want to be clear about how pay is determined. The compensation information posted for this role may be presented as a salary range or a fixed amount depending on the role. In addition to base salary, this role may be eligible for incentive compensation (such as bonus and/or commissions where applicable), along with Stryker’s comprehensive benefits package.

Travel Percentage:

10%

Stryker is one of the world’s leading medical technology companies and, together with its customers, is driven to make healthcare better. We offer innovative products and services in Orthopaedics, Medical and Surgical, and Neurotechnology and Spine that help improve patient and hospital outcomes. We are proud to be named one of the World’s Best Workplaces! For more information, visit: www.stryker.com

Work Flexibility Remote – Role allows you to work the majority to 100% of time from an alternate workplace. These roles could have travel expectations, and you must work within the country of the job requisition location. Field-based – You can expect to regularly work a majority to 100% of time at customer facilities and has a set territory or expectation to travel within a set boundary. Almost all sales roles would likely be qualified as field-based. Onsite – Role is 100% located at a Stryker facility. Some ad hoc flexibility may be available depending on role, level, and job requirements. Manufacturing roles and any role that requires physical presence at the office would qualify under this category. Hybrid – You can expect to regularly work in both an alternate workplace and a Stryker facility. Roles that are partially remote or co-located would qualify as hybrid, and the expectation to be onsite would be defined and agreed upon by your manager/supervisor.