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Principal Electrical Supplier Quality Engineer

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City Of London

On-site

GBP 85,000 - 134,000

Full time

Today
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Job summary

A healthcare technology company is seeking a detail-oriented Supplier Quality Engineer to ensure compliance with standards and enhance product quality. The role involves collaboration with suppliers, conducting audits, and utilizing statistical tools. Ideal candidates have extensive experience in electrical engineering and medical device manufacturing. Competitive salary ranging from $114,800 to $179,500, based on experience and qualifications.

Qualifications

  • 8-10+ years in Electrical Engineering and/or Supplier Quality Engineering roles.
  • 5+ years of experience in medical device manufacturing or related industries.
  • Expertise in supplier quality management processes and manufacturing practices.

Responsibilities

  • Ensure compliance with regulatory standards and QMS requirements.
  • Conduct technical reviews and monitor supplier manufacturing processes.
  • Collaborate with suppliers to exceed reliability and performance standards.

Skills

Communication skills
Problem-solving abilities
Project management skills
Analytical tools proficiency

Education

Bachelor's degree in Engineering or related field

Tools

Microsoft Office
Agile/Oracle
Job description
Overview

Are you passionate about ensuring top-notch quality and compliance in manufacturing? We’re looking for a detail-oriented and proactive Supplier Quality Engineer to join our dynamic team. In this role, you’ll execute activities to ensure compliance with regulatory standards and Quality Management System requirements, conduct technical reviews, and monitor supplier manufacturing processes and quality practices. You’ll collaborate with suppliers to exceed reliability and performance standards, define and approve Production Part Approval Process (PPAP) requirements, and oversee corrective actions, continuous improvements, and adherence to key performance indicators (KPIs). Additionally, you’ll generate supplier performance metrics to support decision-making, apply metrology and statistical tools to solve problems, and travel internationally to conduct audits, quality reviews, and onboard new suppliers. If you thrive in a fast-paced, global environment and want to make a tangible impact on the quality and reliability of our products, we encourage you to apply today!

Responsibilities

This section consolidates the core duties implied by the job description:

  • Execute activities to ensure compliance with regulatory standards and Quality Management System requirements.
  • Conduct technical reviews and monitor supplier manufacturing processes and quality practices.
  • Collaborate with suppliers to exceed reliability and performance standards.
  • Define and approve Production Part Approval Process (PPAP) requirements.
  • Oversee corrective actions, continuous improvements, and adherence to KPIs.
  • Generate supplier performance metrics to support decision-making.
  • Apply metrology and statistical tools to solve problems.
  • Travel internationally to conduct audits, quality reviews, and onboard new suppliers.
Knowledge
  • Expertise in supplier quality management processes and manufacturing practices (e.g., electronics, plastics, metals).
  • Strong understanding of regulatory standards like ISO-13485, ISO-14971, ISO-9001, CFR 820, and FDA requirements.
  • Familiarity with Quality Management Systems (QMS) and Production Part Approval Process (PPAP).
  • Knowledge of metrology, statistical tools (SPC, TQM), and risk management practices.
  • Proficiency in computer tools like Microsoft Office (Intermediate-Advanced) and Agile/Oracle (desirable).
Skills
  • Exceptional communication skills for effective collaboration at all organizational levels.
  • Advanced problem-solving abilities using analytical tools to identify and resolve quality issues.
  • Strong project management skills with the ability to multitask and manage complex initiatives.
  • Ability to generate, analyze, and present supplier performance metrics for decision-making.
  • Proficiency in creating actionable plans and proposals to improve supplier quality.
Behaviors
  • Detail-oriented with a proactive approach to identifying and resolving issues.
  • Commitment to continuous improvement and exceeding performance expectations.
  • Adaptability to work in a global, fast paced, and dynamic environment.
  • Accountability for driving supplier compliance and ensuring quality excellence.
  • Collaborative mindset to work effectively with cross-functional teams and suppliers.
Experiences
  • 8-10+ years in Electrical Engineering and/or Supplier Quality Engineering roles.
  • 5+ years of experience in medical device manufacturing or related industries.
  • Hands-on experience with manufacturing processes for electronics, plastics, and metals.
  • Proven track record in conducting supplier audits and managing compliance initiatives.
  • Experience in leading quality improvement projects and supplier performance reviews.

The individual fulfilling this role must possess the physical capability to sit for extended periods, handle, or manipulate objects, tools, or controls with precision. Additionally, they should be able to stand, walk, reach with hands and arms, stoop, kneel, crouch, and be prepared to engage in domestic and international travel as required by the position.

Why join Hologic?

We are committed to making Hologic the destination for top talent. For you to succeed, we want to enable you with the tools and knowledge required and so we provide comprehensive training when you join as well as continued development and training throughout your career.

Salary: The annualized base salary range for this role is $114,800-179,500 and is bonus eligible. Final compensation packages will depend on factors including relevant experience, skillset, knowledge, education, business needs and market demand.

Agency and Third-Party Recruiter Notice

Agencies that submit a resume to Hologic must have a current executed Hologic Agency Agreement executed by a member of the Human Resource Department. Agencies may only submit candidates to positions for which they have been invited to do so by a Hologic Recruiter. All resumes must be sent to the Hologic Recruiter under these terms or they will not be considered.

Hologic, Inc. is proud to be an Equal Opportunity Employer inclusive of and veterans.

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