Team Lead Quality Engineering

1 Month ago • 15 Years + • Software Development & Engineering

Job Summary

Job Description

The Team Lead Quality Engineering optimizes product quality and manufacturing efficiency by applying advanced statistical methods. This role involves leading a team of 10 quality engineers, driving investigations into non-conformances, implementing CAPA measures, and ensuring compliance with industry standards such as ISO13485. Responsibilities include assessing the impact of design changes on PFMEA, coordinating validation protocols, and developing training programs. The position requires networking with stakeholders and maintaining strategic partnerships. The role is crucial for continuous improvement and regulatory compliance. The candidate will handle in-depth investigations into nonconformances, determining root causes and directing the implementation of robust corrective and preventive actions (CAPA), while monitoring effectiveness and overseeing Non-Conformances (NC) and Quality Notifications (QN) at an advanced level.
Must have:
  • Bachelor’s or Master’s in Engineering or related field.
  • 15 years of experience in Quality Engineering.
  • Extensive knowledge of medical device standards like ISO13485 and 21 CFR 820.
  • Strong networking abilities and communicative persuasion.
Good to have:
  • Experience with continuous improvement tools like Six Sigma and Value stream mapping.

Job Details

Job Title

Team Lead Quality Engineering

Job Description

The Team Lead Quality Engineering plays a critical role in optimizing product quality and manufacturing efficiency by applying advanced statistical methods to solve complex process challenges. You are responsible for a team of 10 quality engineers, promoting a culture of continuous learning in New Product Introduction (NPI) and seamless product transfers.

A key responsibility is leading in-depth investigations into non-conformances, driving the implementation of effective CAPA measures to enhance process reliability ensuring full compliance with industry standards (ISO13485). The role also spearheads initiatives to strengthen supplier quality, collaborating across functions to resolve intricate technical issues.


Your role:

  • Handles in-depth investigations into nonconformances, determining root causes and directing the implementation of robust corrective and preventive actions (CAPA), while monitoring effectiveness and overseeing Non-Conformances (NC) and Quality Notifications (QN) at an advanced level.

  •  Conducts assessment of impact to Process Failure Mode and Effects Analysis (PFMEA) and associated controls in relation to design changes and assists in Manufacturing Process Development and Design Transfer activities.

  • Ensures the coordination of activities within a department, potentially through subordinate supervisors, ensuring accountability for results, including costs, methods, and staffing, demonstrates good working relationships with suppliers and direct shop floor production engineering sustaining experience, and previous experience of participation in several New Product Introductions (NPIs).

  • Possesses complete knowledge of products/services, often leads a cooperative effort to implement robust CAPA measures with a focus on effectiveness and frequently interacts with and functional peer groups on matters between functional areas or customers.

  • Resolves quality non-conformities with R&D, Supplier Engineering and production team for non-conformities inflow reduction.

  • Implements strategic policies while selecting methods and evaluation criteria for obtaining results, manages subordinate staff members, establishes and assures adherence to budgets, schedules, work plans, and performance requirements.

  • Guides the execution of intricate validation protocols, coordinating complex production activities to support validation efforts and ensure rigorous validation outcomes aligned with regulatory requirements.

  • Participates in audits, interprets findings and discusses comprehensive, strategic quality reports with stakeholders, highlighting key achievements, emerging trends, and actionable insights to drive continuous improvement initiatives and ensure regulatory compliance.

  • Develops and delivers specialized training programs on advanced quality standards, methodologies, and best practices, fostering alignment across functions and advancing excellence in operational practices at an expert proficiency level.

  • Networks with key contacts outside own area of expertise and maintain strategic partnerships with external/internal stakeholders.

You're the right fit if:

  • Bachelor’s or Master’s degree in Mechanical Engineering, Electronics Engineering, Science, or a related field.

  • 15 years of experience in Quality Engineering, manufacturing Engineering, or Process Engineering within a manufacturing environment with Quality mindset

  • Extensive knowledge and hands-on experience with medical device standards such as ISO13485 and 21 CFR 820.

  • Preferred experience with continues improvement tools like Six Sigma, Value steam mapping, 7QC tools etc.

  • Strong networking abilities, a proactive approach, and communicative persuasion—capable of clearly and convincingly explaining the necessity of processes or changes, while considering various stakeholder perspectives.


How we work together
We believe that we are better together than apart. This onsite role requires full-time presence at the company’s facilities.

About Philips
We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help the lives of others.
• Learn more about our business.
• Discover our rich and exciting history.
• Learn more about our purpose.

If you’re interested in this role and have many, but not all, of the experiences needed, we encourage you to apply. You may still be the right candidate for this or other opportunities at Philips. Learn more about our commitment to diversity and inclusion here.

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About The Company

At Philips, we believe that every human matters. As a global health-tech leader, we focus on improving people’s health and wellbeing through meaningful innovation. The people who work here share our passion and are motivated to bring this purpose to life.For more than 130 years, we have been creating technologies and innovations that improve people's lives and support healthcare practitioners. Headquartered in the Netherlands and operating in more than 100 countries globally, we focus our advanced technology and deep clinical and consumer insights on Precision Diagnosis, Image Guided Therapy, Enterprise Informatics, Monitoring/ Connected Care, Sleep & Respiratory Care and Personal Health.Together, we deliver better care for more people because we believe that every human matters.

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