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Quality Engineer

Be part of something altogether life-changing!

Working at Cytiva in the Life Sciences industry 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. With associates across 40 countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term.

Cytiva is one of 10 Life Sciences companies of Danaher. Together, we accelerate the discovery, development and delivery of solutions that safeguard and improve human health.

What you’ll do:

  • Support transfer from NPI to high volume manufacturing and develop quality control plans.
  • Implement and maintain, as a team member, Standard Operating Procedures, Process flow charts, Process Control Plans, Process FMEA, and Validations.
  • Manage Non-conformance, CAPA and Complaint (internal and external) processes; ensure root cause analysis and effectively implement robust action plans. Follow-up and verification of CAPAs to ensure no recurrence. Facilitate the closures of these in a timely manner.
  • Provide Manufacturing Quality Trend Charts/Analysis and suggest/implement continuous improvement practices, including appropriate kaizen events on relevant processes based on trends. Support shin Kaizen events and use Lean manufacturing principles, as and when required. Roll out CDT&R, VOP, DRS, PSP, FMEA- utilize DBS to drive continuous improvements.
  • Support Supplier Quality Engineer for driving improvements for Supplier related issues (SCARs), work closely with Purchasing/Sourcing departments to select/maintain/drop suppliers list based on their performance.

Who you are:

  • Bachelor’s degree in an engineering field (e.g. Biomedical, Chemical, Pharma, Industrial, Mechanical, Systems, Quality, Reliability) or equivalent work experience.
  • At least 3 years of experience on a manufacturing or relevant environment
  • Understands and applies Lean Six Sigma tools for problem solving, risk assessment, and process control.
  • Ability to travel 5-15% (domestic and international)
  • Proficient with Microsoft Office Tools (including Outlook, Teams, Excel, and Word).

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

  • Knowledge of the following software/systems: Veeva, SAP, Magic (Enovia)
  • Product line transfers and new product introduction
  • Customer facing technical writing and conflict resolution.

We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees.

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

$80000 / YEARLY (est.)
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$70000K
$90000K

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What You Should Know About Quality Engineer, Cytiva

Are you ready to make a real difference in the Life Sciences industry? As a Quality Engineer at Cytiva, based in beautiful Spartanburg County, SC, you will be at the forefront of developing solutions that transform human health. Imagine working alongside passionate individuals dedicated to real-life impact—from biological research to groundbreaking therapies. In this role, you’ll support the transfer of New Product Innovations to high-volume manufacturing while managing essential quality control plans. You'll implement and maintain Standard Operating Procedures and work on vital processes like Process Control Plans and Validations. Your expertise will shine as you tackle Non-conformance, CAPA, and Complaint processes, ensuring that thorough root cause analysis and robust action plans lead to effective resolutions. We’re looking for someone who’s not only skilled but eager to embrace continuous improvement practices and Lean manufacturing principles. Collaborating closely with the Supplier Quality Engineer, you'll drive enhancements for supplier-related issues and ensure that we're selecting the best partners for our valued customers. If you have a Bachelor’s degree in an engineering field and at least three years of experience in a manufacturing environment, we’d love to hear from you! Here at Cytiva, you'll grow not just professionally but personally, as we empower our team to take on meaningful challenges every day. Join us, and let’s push the boundaries of science together for a healthier tomorrow!

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

As a Quality Engineer at Cytiva, you're responsible for supporting the transfer from New Product Innovations to high-volume manufacturing. You will develop quality control plans, implement Standard Operating Procedures, manage Non-conformance, CAPA, and Complaint processes, and facilitate continuous improvement initiatives utilizing Lean principles. Your technical expertise will be crucial in ensuring product quality and customer satisfaction.

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What qualifications are needed for the Quality Engineer position at Cytiva?

To become a Quality Engineer at Cytiva, you need a Bachelor’s degree in an engineering field such as Biomedical, Chemical, or Mechanical Engineering, or equivalent work experience. You should also have at least 3 years of experience in a manufacturing environment and demonstrable knowledge of Lean Six Sigma tools for problem-solving and risk assessment.

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How does Cytiva support continuous improvement for a Quality Engineer?

At Cytiva, continuous improvement is at the heart of what we do. As a Quality Engineer, you'll have the opportunity to suggest and implement practices based on manufacturing quality trend analysis, support Kaizen events, and utilize Danaher Business System tools to drive enhancements. This collaborative environment encourages you to contribute to the evolution of our processes actively.

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What is the work environment like for Quality Engineers at Cytiva?

The work environment at Cytiva is dynamic and inclusive, filled with diverse professionals who are passionate about making a difference in human health. As a Quality Engineer, you can expect a supportive culture that encourages collaboration and continuous learning, enabling you to grow your skills while working on challenges that matter in a fun and engaging atmosphere.

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Does the Quality Engineer position at Cytiva offer benefits?

Yes, the Quality Engineer position at Cytiva comes with a comprehensive benefits package that includes paid time off, medical/dental/vision insurance, and a 401(k) plan for eligible employees, ensuring work-life balance and wellness for all team members.

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Common Interview Questions for Quality Engineer
What experience do you have with quality control processes?

In answering this question, highlight relevant experiences in managing quality control processes. Discuss specific tools you've used, such as statistical methods or Lean Six Sigma principles, and how they benefitted past projects. Providing quantitative results will showcase your impact.

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Describe a time you identified a quality issue and how you resolved it.

When answering this question, use the STAR method (Situation, Task, Action, Result). Describe the context, the actions you took to investigate and resolve the issue, and the positive outcome. This will demonstrate your problem-solving and analytical skills as a Quality Engineer.

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How do you prioritize tasks in a fast-paced environment?

Explain your approach to prioritization, such as using performance metrics or Lean methodologies. Illustrate with examples where you balanced multiple tasks effectively while ensuring quality standards were met, showing your ability to manage time and resources wisely.

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Can you give an example of a continuous improvement initiative you've led?

Share a specific initiative you've led, describing the process you followed, the stakeholders involved, and the improvements achieved. Focus on how your role as a Quality Engineer added value to the initiative and the techniques you employed, like root cause analysis, to drive results.

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What tools and systems do you have experience with in quality assurance?

Be prepared to discuss the specific software and tools you’ve used, such as Veeva, SAP, or other quality management systems. Highlight how these tools enhanced your work in ensuring product quality and compliance within manufacturing processes.

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How do you ensure compliance with regulatory requirements?

Emphasize your understanding of relevant regulations and how you stay updated. Discuss any experience executing audits, documentation maintenance, and employee training to foster a culture of compliance within a team, showcasing your commitment to quality assurance.

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What role does teamwork play in quality engineering?

Articulate your belief in the importance of teamwork in quality engineering. Provide examples from past experiences where collaboration with other departments, such as production or supply chain, led to improved quality outcomes. This shows your interpersonal skills and ability to work effectively within diverse teams.

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How do you document and report quality findings?

Discuss your preferred documentation methods, such as using software platforms for reporting issues and trends. Mention how clear and concise documentation aids in communication and ensures that stakeholders are informed, ultimately enhancing product quality and compliance.

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What strategies do you use to manage supplier quality issues?

Provide insight into your experience managing supplier quality, discussing approaches like regular supplier audits, performance reviews, and communication techniques that have ensured quality. Explain how you would apply this at Cytiva to drive improvements in supplier-related issues.

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Why do you want to work for Cytiva as a Quality Engineer?

Express your passion for the Life Sciences industry and how Cytiva's mission aligns with your values. Talk about your enthusiasm for contributing to meaningful projects that improve human health, highlighting your eagerness to grow and learn within such a supportive and innovative environment.

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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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