Senior Design Quality Engineer
Senior Design Quality Engineer

Senior Design Quality Engineer

Belfast Full-Time 48000 - 72000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Join a dynamic team to ensure top-notch quality in medical device design and development.
  • Company: Stryker is a leading medical technology company dedicated to improving healthcare.
  • Benefits: Enjoy hybrid work options, competitive pay, and opportunities for professional growth.
  • Why this job: Make a real impact on patient safety while working in a collaborative and innovative environment.
  • Qualifications: Bachelor's in Engineering and 2+ years in a regulated quality or engineering role required.
  • Other info: Ideal for those passionate about medical devices and eager to advance their technical skills.

The predicted salary is between 48000 - 72000 £ per year.

Position SummarySenior Design Quality Engineer (Hybrid)Stryker is hiring a Senior Design Quality Engineer in Redmond-WA, to support our Medical Business. You will work as the Design Quality Engineering partner within a cross-functional product development team to enable timely launch of the highest quality products that meets and exceeds customer and stakeholder expectations in support of a successful product lifecycle of a medical device. You will serve as a representative for the Quality Management System at all times and drive continuous process improvement.What you will do:Participate in the product development process by ensuring that all the quality data streams are fully comprehended and that the voice of the customer, as heard through these data streams (complaints, non-conforming records, verified failures, etc.), is a design input and consideration.Lead product safety Risk Management activities, including, characterization and estimation of design risks, which includes both the appropriate control activities and proper identification in downstream design outputs. Develop Risk Management File deliverables including Product Hazard Analysis, design failure modes and effects analysis [DFMEA], Critical to Quality characteristics on specifications, Risk Assessments for issues impacting distributed product, etc.Develop validation strategies for projects that are consistent with design validation policies and procedures. Provide technical direction and approval of validation plans, protocols, reports.Provide technical direction in optimization of test plans, test methods and sampling.Advocate and lead the execution of initiatives & projects to improve Quality throughout the organizationEstablish appropriate field performance trending metrics using standardized reporting mechanisms, analyze results to identify emerging trends and improvement opportunities, and reporting for production and post-production monitoring of new products after launch.Provide Quality leadership to drive the timely resolution of quality issues impacting assigned product lines and participate in the CAPA process as task owner/contributor as appropriate and necessary. Advise on risk management investigations for HHE, PFAs, NCs and CAPAs or other post-market issues as needed.Participate in internal & external audits with regulatory representatives, providing effective narrative and description of topic of expertise and overview of product development within the Design Controls process.As a Senior level engineer, seek out learning opportunities across Stryker to advance technical skills and knowledge and develop subject matter expertiseWhat you will need:Bachelors Degree in Engineering (biomedical engineering preferred)2+ years of experience working in a highly regulated environment, quality, manufacturing, or engineering.Strong knowledge of medical device industry policies and regulations.Prior experience working with electro-mechanical commodities and embedded software in a product development capacityKnowledge of quality tools for process capability, root cause investigation, developing sampling plans, test method validation, or other Quality tasksKnowledge of good design practices, specification development, industry standards, etc. #J-18808-Ljbffr

Senior Design Quality Engineer employer: JobLeads GmbH

Stryker is an exceptional employer that fosters a collaborative and innovative work culture in Redmond, WA, where employees are empowered to contribute to the development of high-quality medical devices. With a strong commitment to employee growth, Stryker offers numerous learning opportunities and encourages continuous improvement, ensuring that team members can advance their technical skills and expertise while making a meaningful impact on patient care. The hybrid work model provides flexibility, allowing for a balanced work-life integration in a vibrant community known for its technological advancements.
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Contact Detail:

JobLeads GmbH Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Senior Design Quality Engineer

✨Tip Number 1

Network with professionals in the medical device industry, especially those who work at Stryker or similar companies. Attend industry conferences or webinars to connect with potential colleagues and learn more about the company culture.

✨Tip Number 2

Familiarise yourself with the latest regulations and standards in the medical device sector. Being well-versed in these can help you demonstrate your expertise during interviews and show that you're proactive about staying updated.

✨Tip Number 3

Prepare to discuss specific examples of how you've contributed to quality improvement initiatives in past roles. Highlighting your hands-on experience with risk management and validation strategies will set you apart from other candidates.

✨Tip Number 4

Research Stryker's recent projects and innovations in the medical device field. Being able to speak knowledgeably about their products and how you can contribute to their success will make a strong impression during your interview.

We think you need these skills to ace Senior Design Quality Engineer

Risk Management
Design Failure Modes and Effects Analysis (DFMEA)
Product Hazard Analysis
Validation Strategies Development
Technical Direction in Test Methods
Quality Management System Knowledge
Regulatory Compliance
Root Cause Analysis
Process Improvement
Statistical Process Control (SPC)
Field Performance Trending Metrics
Cross-Functional Team Collaboration
Medical Device Industry Standards
Electro-Mechanical Product Development
Embedded Software Knowledge

Some tips for your application 🫡

Understand the Role: Before applying, make sure to thoroughly understand the responsibilities and requirements of the Senior Design Quality Engineer position. Tailor your application to highlight relevant experiences that align with the job description.

Highlight Relevant Experience: In your CV and cover letter, emphasise your experience in quality engineering, particularly in regulated environments. Mention specific projects where you contributed to product safety risk management or validation strategies.

Showcase Technical Skills: Detail your technical skills related to medical devices, such as knowledge of DFMEA, risk assessments, and quality tools. Use examples to demonstrate how you've applied these skills in past roles.

Craft a Compelling Cover Letter: Write a cover letter that not only summarises your qualifications but also conveys your passion for quality engineering in the medical device industry. Discuss how you can contribute to Stryker's mission and values.

How to prepare for a job interview at JobLeads GmbH

✨Understand the Role and Responsibilities

Make sure you thoroughly understand the job description and the key responsibilities of a Senior Design Quality Engineer. Familiarise yourself with terms like Risk Management, DFMEA, and CAPA, as these will likely come up during the interview.

✨Showcase Your Experience

Prepare to discuss your previous experience in quality engineering, especially in regulated environments. Be ready to provide specific examples of how you've contributed to product development and quality improvement initiatives.

✨Demonstrate Knowledge of Industry Standards

Brush up on relevant medical device industry policies and regulations. Being able to discuss these confidently will show that you are well-prepared and knowledgeable about the field.

✨Ask Insightful Questions

Prepare thoughtful questions to ask the interviewer about the company's quality management practices and how they approach continuous improvement. This shows your genuine interest in the role and helps you assess if the company is the right fit for you.

Senior Design Quality Engineer
JobLeads GmbH
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