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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 www.danaher.com.

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.

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What You Should Know About Senior Supplier Quality Engineer, Danaher

Cytiva is seeking a Senior Supplier Quality Engineer to join our dynamic team in Pensacola, Florida. Are you ready to accelerate your potential and make a genuine impact within the life sciences sector? At Cytiva, a proud member of Danaher’s diverse family of operating companies, we’re dedicated to innovating and providing solutions that save lives. In this role, you will manage supplier defects, ensure compliance, and maintain Quality Management System processes while driving improvements to our External PPM Defects core value driver. As part of our Bioprocess Filtration Supplier Quality Team, you’ll focus on supplier qualifications, manage corrective actions, and provide input during supplier audits. With an emphasis on collaboration, you’ll develop and execute corrective action plans to resolve non-conformance issues, ensuring that our suppliers adhere to the highest QMS and regulatory requirements. What makes this position unique is the genuine culture of belonging and commitment to continuous improvement at Cytiva. Here, you’ll tackle meaningful challenges with supportive colleagues who care about each other and our customers' patients. If you have a bachelor’s degree in a relevant field and at least five years of quality experience, including three years focused on supplier management, we'd love to see you thrive in this key role. Join us in advancing future therapeutics from discovery to delivery, and become part of a team that's shaping the future of health and science!

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

As a Senior Supplier Quality Engineer at Cytiva, your responsibilities will revolve around managing supplier defects and ensuring compliance with Quality Management System processes. You'll handle supplier qualifications, manage the corrective actions process, and conduct audits according to approved schedules. Collaboration with suppliers to develop corrective and preventive action plans is vital to ensure adherence to regulatory requirements.

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

To qualify for the Senior Supplier Quality Engineer position at Cytiva, candidates should hold a bachelor's degree in a relevant field such as mechanical or chemical engineering, or possess equivalent experience in a similar industry. Additionally, at least five years of quality experience and three years specifically in supplier onboarding and auditing are required.

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How does Cytiva support its Senior Supplier Quality Engineers in their development?

Cytiva is committed to the continuous improvement and professional development of its employees. As a Senior Supplier Quality Engineer, you’ll thrive in a culture that emphasizes collaboration and provides opportunities for growth in life sciences, diagnostics, and biotechnology sectors. Employees at Cytiva benefit from comprehensive training programs and a supportive environment that encourages innovative thinking.

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What kind of experience do you need for the Senior Supplier Quality Engineer position at Cytiva?

Candidates for the Senior Supplier Quality Engineer role at Cytiva should have a minimum of five years of experience in quality, focusing on supplier onboarding, communication, and audits. Experience with Quality Management Systems, cGMP, and continuous improvement methodologies is also essential, as is familiarity with the medical device and pharmaceutical sectors.

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Is travel required for the Senior Supplier Quality Engineer role at Cytiva?

Yes, for the Senior Supplier Quality Engineer position at Cytiva, some travel is required. You will need to travel approximately 10-15% of the time for supplier audits and assessments, which allows for up-close interactions with the suppliers to ensure quality and compliance.

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

Focus on discussing specific examples from your previous roles where you managed supplier quality issues, how you communicated with suppliers, and what strategies you implemented to improve overall performance.

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What steps do you take to resolve non-conformance issues with suppliers?

Explain your approach to developing Corrective and Preventive Action (CAPA) plans. Highlight your analytical skills, your ability to perform root cause investigations, and how you ensure compliance with both internal and external regulations.

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What do you understand by Quality Management Systems and how have you applied them?

Discuss your familiarity with Quality Management Systems like ISO 9001, including how you’ve previously implemented these standards within your team or organization to achieve regulatory compliance and enhance product quality.

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How do you prioritize your tasks when multiple suppliers have quality issues?

You might explain your methodology for assessing the impact of issues, referencing tools or frameworks you've used to prioritize urgent matters and ensure that critical quality issues get addressed promptly.

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Describe a challenging audit you conducted and how you handled it.

Share an example of an audit, focusing on the challenges you faced, such as resistance or limited documentation, and how you managed the situation to ensure thorough findings and compliance.

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How do you ensure effective communication with suppliers?

You can emphasize your proactive communication style, how you establish clear expectations, and the importance of maintaining a constructive relationship to foster transparency and quick issue resolution.

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What is your experience with cross-functional teams in quality assurance?

Reference any collaborative projects where you worked with different departments, focusing on how collective efforts led to quality improvements and shared responsibility for supplier outcomes.

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Can you explain the significance of CAPA in supplier quality?

Detail how Corrective and Preventive Action processes help to identify, address, and prevent quality issues within the supply chain, ensuring that suppliers meet the requisite standards and contribute positively to overall product quality.

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How do you stay updated with industry trends and regulatory changes?

Discuss your commitment to professional development through reading industry publications, attending seminars, or participating in relevant professional organizations to stay informed about best practices and regulatory standards.

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

Your answer should reflect your enthusiasm for the role, aligning your personal values and career goals with Cytiva's mission and commitment to advancing life sciences, showcasing your drive to contribute to meaningful work.

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Our globally diverse team of 80,000 associates is united by our Shared Purpose—Helping Realize Life’s Potential. This Shared Purpose is at the core of our deep commitment to developing innovations in science and technology that make a difference i...

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March 30, 2025

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