Manufacturing Engineer

Reposted 18 Days Ago
Be an Early Applicant
Logan, UT, USA
In-Office
Expert/Leader
Biotech
The Role
Lead continuous improvement and problem-solving projects within the value stream. Design, install, validate, and qualify manufacturing equipment (IQ/OQ/PQ). Apply LEAN tools, DOE, statistical analysis, PFMEA, root cause analysis, and change control. Lead cross-functional teams to resolve technical issues while ensuring cGMP compliance and improving safety, quality, production, and cost efficiency.
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?

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 Manufacturing Engineer is responsible for problem solving and continuous improvement projects within the value stream.

The position reports to the Senior Manager, Manufacturing Engineering and is part of the Engineering Department located in Logan, Utah and will be an on-site role.

What you will do:

  • Actively engage and support engineering priorities in response to manufacturing and plant priorities related to safety, quality, production, and cost/efficiency
  • Develop, lead or participate in various process improvement projects. Drive continuous improvement (LEAN) initiatives through application of sound engineering/reliability program elements and a data driven approach
  • Design, install, validate, and qualify new equipment to address key gaps in manufacturing and ensure that engineering support is performed in compliance with cGMP Regulations and Company Policies/Procedures
  • Lead cross functional project teams with project management and change management. Lead qualification and validation project activities including the creation and execution of validation protocols (IQ/OQ/PQ) and reports
  • Lead cross functional teams in Problem Solving, Root Cause Analysis, Value Stream Mapping, PFMEA, Kaizen, Change Control and identifying, analyzing, and driving technical issues to resolution

Who you are

  • Bachelor's Degree in a related engineering field or equivalent experience and 9+ years of experience in manufacturing/engineering
  • Thrives well working within a cross-functional team environment with excellent oral and written communication
  • Proven ability to apply strong fundamental scientific and engineering skills to evaluate and develop processes and offer practical solutions to technical challenges
  • Proficient in statistical data analysis and DOE
  • Mechanical proficiency and hands-on experience with machine design a plus

#LI-MP6

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].

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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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