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Engineer II Custom Consumable

Danaher

Engineer II Custom Consumable

full-timePosted: Jan 13, 2026

Job Description

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 Final Fill 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 final fill bioprocessing. Experience with single use assemblies for monoclonal antibody manufacturing.

#LI-SL21

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.

Locations

  • Medemblik, Netherlands

Salary

Estimated Salary Rangemedium confidence

85,000 - 150,000 EUR / yearly

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • CAD solid modeling (SolidWorks, CREO)intermediate
  • Technical documentationintermediate
  • GMP and regulatory complianceintermediate

Required Qualifications

  • Bachelor’s degree in Mechanical, Plastics, Bio, or Biomedical Engineering (experience)
  • 2+ years in mechanical engineering, biotech, or related fields (experience)

Responsibilities

  • 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

Benefits

  • general: Culture of belonging
  • general: Danaher Business System continuous improvement

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Danaher logo

Engineer II Custom Consumable

Danaher

Engineer II Custom Consumable

full-timePosted: Jan 13, 2026

Job Description

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 Final Fill 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 final fill bioprocessing. Experience with single use assemblies for monoclonal antibody manufacturing.

#LI-SL21

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.

Locations

  • Medemblik, Netherlands

Salary

Estimated Salary Rangemedium confidence

85,000 - 150,000 EUR / yearly

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • CAD solid modeling (SolidWorks, CREO)intermediate
  • Technical documentationintermediate
  • GMP and regulatory complianceintermediate

Required Qualifications

  • Bachelor’s degree in Mechanical, Plastics, Bio, or Biomedical Engineering (experience)
  • 2+ years in mechanical engineering, biotech, or related fields (experience)

Responsibilities

  • 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

Benefits

  • general: Culture of belonging
  • general: Danaher Business System continuous improvement

Target Your Resume for "Engineer II Custom Consumable" , Danaher

Get personalized recommendations to optimize your resume specifically for Engineer II Custom Consumable. Takes only 15 seconds!

AI-powered keyword optimization
Skills matching & gap analysis
Experience alignment suggestions

Check Your ATS Score for "Engineer II Custom Consumable" , Danaher

Find out how well your resume matches this job's requirements. Get comprehensive analysis including ATS compatibility, keyword matching, skill gaps, and personalized recommendations.

ATS compatibility check
Keyword optimization analysis
Skill matching & gap identification
Format & readability score
Quiz Challenge

Answer 10 quick questions to check your fit for Engineer II Custom Consumable @ Danaher.

10 Questions
~2 Minutes
Instant Score

Related Books and Jobs

No related jobs found at the moment.