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Engineer Custom Consumable

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 Custom Consumable Engineer is responsible for designing and developing custom single use assemblies for bioprocessing applications.

This position reports to the Upstream Consumable Engineering Manager and is part of Hardware Solutions operating company located in Marlborough and will be an on-site role.

What You'll Do:

  • Design, test, and release single-use consumables (components, packaging, tooling, fixtures).
  • Develop and maintain project documentation (testing protocols, risk analyses, design docs) within the QMS.
  • Own project timelines and keep stakeholders updated.
  • Follow QMS and Change Control processes to ensure quality and compliance.
  • Use engineering judgment and creativity to continually improve processes and product outcomes.

Who You Are:

  • Education: Bachelor's degree in Mechanical, Plastics, Bio, or Biomedical Engineering.
  • Experience: 2+ years in mechanical engineering, biotech, or related fields.
  • Skilled in meeting customer requirements and collaborating across departments.
  • Proficient in CAD solid modeling (SolidWorks, CREO) and technical documentation.
  • Familiar with GMP and regulatory requirements, ensuring accurate documentation and compliance.

Travel, Motor Vehicle Record & Physical/Environment Requirements:

  • Ability to travel 15% within the US or internationally.
  • Must have a valid driver's license with an acceptable driving record
  • Ability to lift, move or carry equipment up to 25lb, any other physical requirements

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

  • Masters degree in plastic engineering, bio or mechanical. 4+ years experience in bioprocessing. Experience with single use assemblies for monoclonal antibody manufacturing.

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 to request accommodation.

Average salary estimate

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

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What You Should Know About Engineer Custom Consumable, Cytiva

Are you ready to make a profound impact on the world of life sciences and biotechnology? As an Engineer Custom Consumable at Cytiva in Marlborough, MA, you’ll be at the heart of innovation that saves lives. At Cytiva, one of the operating companies within Danaher, we take pride in our mission to transform human health through our cutting-edge solutions in bioprocessing. Here, you'll have the opportunity to design and develop custom single-use assemblies while engaging collaboratively with exceptional teams. You'll take on responsibilities that include creating detailed project documentation, managing timelines, and ensuring compliance with QMS and Change Control processes, which is crucial in our industry. Your expertise in mechanical or biomedical engineering will shine as you utilize CAD solid modeling software like SolidWorks or CREO. We emphasize continuous improvement and value the unique viewpoints of our team members. Join us, and you’ll work on challenges that matter, surrounded by people committed to transforming science into impactful results. Whether you have a strong background in mechanical engineering or relevant biotech experience, we welcome dedicated individuals ready to contribute to groundbreaking advancements. This on-site position offers a dynamic work environment where your engineering judgment and creativity can flourish. Take the first step toward a life-changing career—be part of a team that prioritizes innovation in life sciences at Cytiva!

Frequently Asked Questions (FAQs) for Engineer Custom Consumable Role at Cytiva
What are the core responsibilities of an Engineer Custom Consumable at Cytiva?

The Engineer Custom Consumable at Cytiva is primarily responsible for designing and developing custom single-use consumables for bioprocessing applications. This includes tasks such as creating and testing the assemblies, maintaining project documentation like testing protocols and risk analyses, and ensuring projects follow quality management standards.

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What qualifications are required for the Engineer Custom Consumable position at Cytiva?

To qualify for the Engineer Custom Consumable position at Cytiva, candidates typically need a Bachelor’s degree in Mechanical, Plastics, Bio, or Biomedical Engineering, along with at least two years of experience in mechanical engineering, biotech, or related fields. Familiarity with CAD solid modeling and regulatory compliance is essential.

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How does the Engineer Custom Consumable role contribute to the mission of Cytiva?

The Engineer Custom Consumable plays a crucial role in advancing Cytiva's mission by developing innovative solutions that enable bioprocessing applications. This contributes directly to the production of life-saving therapies and treatments, impacting human health positively.

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What tools and skills are important for the Engineer Custom Consumable at Cytiva?

For the Engineer Custom Consumable role at Cytiva, proficiency in CAD software (such as SolidWorks or CREO) is critical. Additionally, skills in technical documentation and familiarity with GMP and regulatory guidelines will help ensure product quality and compliance.

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What is the work culture like at Cytiva for an Engineer Custom Consumable?

At Cytiva, the work culture fosters a sense of belonging and encourages diverse viewpoints. Employees are motivated by a shared commitment to innovation and are supported in their professional growth, making it an inspiring environment for an Engineer Custom Consumable.

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Common Interview Questions for Engineer Custom Consumable
Can you describe your experience with CAD solid modeling in relation to engineering custom consumables?

In answering this question, you should highlight specific projects where you've used CAD software like SolidWorks or CREO to create designs. Discuss the challenges faced and how your designs contributed to project goals, emphasizing technical skills and innovative solutions.

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What approach do you take to ensure compliance with quality management systems?

Your response should outline your understanding of quality management principles and your experience in maintaining documentation and processes that adhere to these standards, particularly how you have ensured project compliance with QMS in past roles.

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How do you manage timelines and deliverables in engineering projects?

Discuss your project management skills, including any tools you use to track progress and how you communicate with stakeholders. Give examples of past projects where you successfully met deadlines while maintaining quality.

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What strategies do you use to foster collaboration across departments?

Share your experiences working in cross-functional teams, emphasizing techniques you've employed to facilitate communication, share goals, and resolve conflicts that may arise during project execution.

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Can you give an example of a time when your engineering judgment led to a significant improvement in a product or process?

Here, provide a specific example where your creativity and analytical skills helped to improve an existing process or product. Discuss the impact of your contribution and be prepared to explain the decision-making process that led to your solution.

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Describe your experience with regulatory requirements in the biotech industry.

Explain your familiarity with regulatory standards and any experience you have had in ensuring product designs meet these regulations, highlighting specific guidelines you've interacted with or compliance challenges you've navigated.

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How do you keep current with the latest trends and technologies in bioprocessing?

Discuss the professional development methods you employ, such as attending industry conferences, participating in relevant workshops, or following key thought leaders and publications in life sciences and biotech.

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What motivates you to work in the field of life sciences and biotechnology?

Reflect on your passion for science and your desire to contribute to meaningful advancements that impact human health. Consider connecting specific experiences or values that drive your motivation.

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How do you prioritize quality when developing custom consumables?

Focus on the importance of attention to detail and thorough testing in your design process. Provide examples of how you have implemented quality checks and balances to ensure that the final products meet or exceed expectations.

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What challenges do you foresee in the Engineer Custom Consumable role, and how would you approach them?

Identify potential challenges, such as keeping up with changing regulatory landscapes or managing tight project timelines. Describe your methods for strategizing solutions, emphasizing proactive planning and adaptability.

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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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Full-time, on-site
DATE POSTED
April 13, 2025

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