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Senior Supplier Quality Engineer

Bring more to life.

Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?

At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact. 

You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.

Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.

At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career.

Learn about the Danaher Business System which makes everything possible.

The Senior Supplier Quality Engineer for Cytiva is responsible to manage supplier defects, be compliant and maintain our Quality Management System processes and records as well as drive improvement to our core value driver, External PPM Defects. 

This position is part of the Bioprocess Filtration Supplier Quality Team located in Penscola, FL and will be onsite. At Cytiva, our vision is, to advance future therapeutics from discovery to delivery. 

What you will do:

  • Supplier qualification, including supplier process qualification (SPQ) for Type I (critical) supplier.

  • Manage the supplier corrective actions process (SCAR) and supplier change requests (SCR).

  • Provide input and conducting supplier audits as on approved supplier audit schedule.

  • Develop and execute Corrective and Preventive Action plans with suppliers to resolve non-conformance issues (QE Complaints and Deviations).

  • Ensure supplier compliance to QMS and regulatory requirements through supplier monitoring process.

Who you are:

  • Bachelor’s degree in applicable field (e.g. mechanical engineering, chemical engineering or general life sciences) or equivalent by experience in Quality in a similar BU/Industry.

  • Minimum 5 years of Quality experience preferably in applicable or similar field

  • Minimum 3 years of experience in supplier on-boarding, supplier auditing, and supplier communications. Experience with supplier communication and supplier auditing.

  • Demonstrated knowledge of Quality Management System (ISO 9001 or equivalent), cGMP, continuous improvement methodologies, and Manufacturing Process Control (MPC)

  • Effective problem solver with the skills to lead Root Cause investigations / CAPA plans and influence others cross-functionally.

    ·

Travel, Motor Vehicle Record & Physical/Environment Requirements:

  • Ability to travel around 10-15% for supplier audits and GEMBA walks.

It would be a plus if you also possess previous experience in:

  • Medical Device, e.g. ISO 13485
  • Pharmaceutical
  • Chemical
  • Automotive, e.g. IATF 16949
  • Speaking fluent Spanish

Cytiva, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it’s a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info .

Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. 

For more information, visit .

Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. We value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.

The EEO posters are available here .

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us at applyassistance@danaher.com to request accommodation.

Average salary estimate

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What You Should Know About Senior Supplier Quality Engineer, Cytiva

Are you ready to take your career to the next level as a Senior Supplier Quality Engineer at Cytiva? We’re looking for someone passionate about life sciences, diagnostics, and biotechnology who can help us make a real difference. At Cytiva, part of the Danaher family, our mission is all about saving lives through innovative solutions. You’ll be working in our Miami-Dade County, FL facility, where you’ll thrive in a culture that promotes belonging and inclusivity. Your primary role will be managing supplier defects and maintaining compliance with our Quality Management System while driving improvements to our External PPM Defects. Engaging with our incredible customers, you will ensure the delivery of life-saving products from biological research to innovative vaccines. The position highlights the importance of effective communication and collaboration, as you conduct supplier audits and develop corrective action plans to resolve non-conformance issues. We need someone who has a bachelor’s degree in a relevant field and at least five years of quality experience, particularly in supplier onboarding and auditing. If you are an effective problem-solver, skilled in leading root cause investigations and cross-functional influence, we would love to hear from you! Join us at Cytiva and be part of a team that not only cares for each other but also for patients worldwide. Take the next step for a life-changing career today!

Frequently Asked Questions (FAQs) for Senior Supplier Quality Engineer Role at Cytiva
What are the main responsibilities of a Senior Supplier Quality Engineer at Cytiva?

As a Senior Supplier Quality Engineer at Cytiva, you'll handle supplier qualifications and manage the supplier corrective actions process. Additionally, you'll provide input on supplier audits, develop corrective and preventive action plans for non-conformance, and ensure supplier compliance with quality and regulatory standards. Your role is crucial in driving improvements and maintaining our Quality Management System.

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What qualifications are required to become a Senior Supplier Quality Engineer at Cytiva?

To qualify as a Senior Supplier Quality Engineer at Cytiva, candidates need a bachelor's degree in a related field, such as engineering or life sciences, along with a minimum of five years of quality experience. You'll benefit from having experience in supplier onboarding, auditing, and knowledge of quality management systems, especially ISO standards and cGMP regulations.

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How does the work of a Senior Supplier Quality Engineer impact patient health at Cytiva?

The work of a Senior Supplier Quality Engineer directly impacts patient health by ensuring that suppliers meet stringent quality and regulatory standards. By managing supplier defects and conducting audits, you'll help ensure that life-saving products and therapies are of the highest quality, ultimately supporting Cytiva's mission to advance therapeutics that save lives.

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What is the company culture like at Cytiva for a Senior Supplier Quality Engineer?

Cytiva fosters a culture of belonging, where diverse viewpoints are valued. As a Senior Supplier Quality Engineer, you'll be part of a supportive environment that encourages personal and professional development, allowing you to thrive and make a real impact within the team and beyond.

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What travel requirements are expected for the Senior Supplier Quality Engineer at Cytiva?

The Senior Supplier Quality Engineer at Cytiva is expected to travel approximately 10-15% of the time. This travel is primarily for supplier audits and GEMBA walks, allowing you to engage directly with suppliers and assess their quality processes.

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Common Interview Questions for Senior Supplier Quality Engineer
Can you describe your experience with supplier quality management?

In your answer, focus on specific instances where you managed supplier quality processes, detailing how you evaluated suppliers, addressed defects, and implemented corrective actions. Make sure to highlight your methodologies and understanding of quality standards.

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How do you approach corrective and preventive action (CAPA) plans?

Discuss your structured approach to developing CAPA plans, including how you identify root causes, create action steps, and follow up to ensure compliance. Use examples from your past experience to demonstrate your effectiveness in previous roles.

Join Rise to see the full answer
What strategies do you employ for supplier audits?

Explain how you prepare for supplier audits by reviewing documentation, setting objectives, and ensuring the necessary resources are available. Discuss the importance of communication and transparency during the audit process, and how you work to foster good relationships with suppliers.

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Describe a challenging supplier quality issue you've faced and how you resolved it?

Use the STAR method (Situation, Task, Action, Result) to outline a specific challenge. Detail how you identified the issue, the steps you took to facilitate resolution, and any long-term improvements you implemented as a result.

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How do you keep up with changes in quality management regulations?

Talk about the resources you utilize, such as industry publications, forums, and professional groups. Highlight any training or certifications you maintain to stay informed about updates in regulations, ISO standards, and best practices in quality management.

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What role does data analysis play in your decision-making process?

Emphasize your analytical skills and how you leverage data to support quality decisions. Give examples of how you have used data to identify trends, monitor supplier performance, or evaluate the effectiveness of quality initiatives.

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Can you give an example of how you improved a quality process?

Highlight a specific process you’ve improved, detailing the measures you implemented, the timeframe for changes, and the impact of those changes on overall quality metrics. Show your ability to drive continuous improvement.

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How do you handle conflicts with suppliers?

Describe your approach to resolving conflicts diplomatically and effectively, ensuring that you maintain professional relationships while still advocating for compliant quality measures. Share a relevant experience to illustrate your method.

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What systems or tools do you use for quality management?

Discuss your familiarity with specific quality management systems (QMS) tools that you've used, like ISO 9001 software, and how you've applied these to improve quality processes. Mention any particular software that you're proficient with.

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Why do you want to work as a Senior Supplier Quality Engineer at Cytiva?

Express your interest in Cytiva’s mission and values, and how they align with your career objectives. Discuss your enthusiasm for working in the life sciences industry and your commitment to improving quality processes that positively impact patient health.

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Cytiva is a global biotechnology leader dedicated to helping customers discover and commercialize the next generation of therapeutics. We bring dedicated technical expertise and a broad portfolio of tools, technologies, and services that enable th...

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April 13, 2025

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