Lead Manufacturing Engineer (Global Technical Operations, Single Use Systems - Fluid Management)

Reposted 13 Days Ago
Be an Early Applicant
2 Locations
In-Office
Mid level
Biotech
The Role
The Lead Manufacturing Engineer drives global manufacturing initiatives, improves processes, supports new product introductions and project planning, ensuring compliance and quality.
Summary Generated by Built In

Bring more to life.

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

Within Danaher the work our life science businesses do 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. 

We have over 21,000 associates across more than 10 life sciences businesses. These businesses empower our customers to develop diverse and impactful innovations — from investigating the causes of disease, creating therapies and vaccines, protecting fluid filtration on airplanes, testing food and water, to advancing pharmaceuticals and biopharmaceuticals.

Learn about the Danaher Business System which makes everything possible.

The Lead Manufacturing Engineer is responsible for supporting global manufacturing initiatives consisting of process innovation projects, introduction of new products, supporting global multi-site process standardization, and digitization of manufacturing processes, and transfers of production into various Cytiva operations business units globally.

This position reports to the Sr. Manager of Global Technical Operations and Engineering and will be an on-site role in Duncan. SC.

What you will do:

  • Partner with global strategic, technical, and operational manufacturing teams to improve existing processes and implement innovative manufacturing solutions.
  • Collaborate closely with RD&E and cross‑functional stakeholders to define, document, and deliver manufacturing and operations project requirements.
  • Define equipment and machine requirements and work with internal and external machine builders to support manufacturing needs.
  • Represent manufacturing on global cross‑functional project and process development teams while driving supply chain rigor, product lifecycle management, and risk mitigation.
  • Ensure regulatory and quality compliance by leading validation and verification activities and driving improvements in product quality and manufacturing productivity.

Who you are:

  • Bachelor’s degree in Mechanical Engineering, Electrical Engineering, Industrial Engineering, or a related technical field.
  • Prefer minimum of 3+ years of progressive, post‑bachelor experience in a related engineering or technical role.
  • Prefer at least 3+ years of experience in production or engineering within a regulated, medical device, or similar industry.
  • Prefer 3+ years of experience in project planning and project management, successfully managing multiple projects concurrently.
  • Prefer 3+ years of hands‑on experience with innovation, development, testing, and qualification activities.

Travel, Motor Vehicle Record & Physical/Environment Requirements:

  • Ability to travel – 15% travel globally
  • Must have a valid driver’s license with an acceptable driving record
  • Ability to lift, move or carry equipment up to 35lb, any other physical requirements

Within Danaher Life Sciences, we offer 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.

This job is also eligible for bonus/incentive pay.

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

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company’s sole discretion, consistent with the law.

#LI-ND19

#thisisbelonging

#thebestteamisdiverse

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.

The U.S. EEO posters are available here.

We comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact:1-202-419-7762 or [email protected].

Skills Required

  • Bachelor's degree in Mechanical Engineering, Electrical Engineering, Industrial Engineering, or related field
  • Minimum of 3+ years experience in related engineering or technical role
  • 3+ years experience in production or engineering within a regulated medical device industry
  • 3+ years experience in project planning and management
  • 3+ years hands-on experience with innovation, development, testing, and qualification activities

Cepheid Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Cepheid and has not been reviewed or approved by Cepheid.

  • Leave & Time Off Breadth PTO and paid holidays are portrayed as robust, with formal programs and mentions of generous time off and rollover in some cases. This breadth supports a positive view of time-off availability.
  • Healthcare Strength Core medical, dental, and vision coverage is highlighted repeatedly and is viewed as comprehensive for regular full‑time employees. Descriptions such as “good” or “great” benefits reinforce the strength of the health coverage.
  • Retirement Support A 401(k) plan with company matching is consistently included as part of the package. The presence of matching contributions strengthens perceived retirement readiness.

Cepheid Insights

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The Company
HQ: Sunnyvale, CA
4,883 Employees
Year Founded: 1996

What We Do

Cepheid is dedicated to improving healthcare by pioneering molecular diagnostics that combine speed, accuracy, and flexibility. The company's GeneXpert® systems and Xpert® tests automate highly complex and time-consuming manual procedures, providing A Better Way for institutions of any size to perform world-class PCR testing. Cepheid’s broad test portfolio spans respiratory infections, blood virology, women’s and sexual health, TB and emerging infectious diseases, healthcare-associated infectious diseases, oncology and human genetics. The company’s solutions deliver actionable results where they are needed most – from central laboratories and hospitals to near-patient settings. For more information, visit http://www.cepheid.com.

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