Quality Engineer

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 Quality Engineer is responsible for ensuring the quality of membrane products through facilitating cross-functional execution of the QMS (Quality Management System), setting inspection processes, implementing quality control measures and identifying statistical trends. Additionally, the Quality Engineer addresses customer complaints, resolves production quality issues, collaborates with cross-functional teams to identify root causes, and drives continuous improvements to deliver high-quality products. Additionally, they support new product introduction projects.

This position reports to the Sr. Quality Engineer Team Leader and is part of the Quality Engineering Team located in Pensacola, FL and will be an on-site role.

What you will do:

• Investigate and correct root causes of product failures occurring in the field.
• Ensure design control process compliance throughout whole product lifecycle and deliver training on quality process guiding colleagues and team members as required.
• Guide and overall support product risk management process.
• Establish, maintain, monitor QMS process performance with data analysis and lead quality improvement project from system level.
• Responsible for issuing or reviewing and approving deviations, document changes, validation activities and change controls.
   

Who you are:

• Bachelor’s degree in science, engineering, or technical field required
• 1+ years of relevant experience in biomedical or medical device manufacturing preferred
• Uses analytical mind and data analysis (Excel) to creatively and pragmatically solve problems, comes up with solutions
• Knowledge of quality standards ISO 9001 and ISO 13485
• Curious and coachable
   

Travel, Motor Vehicle Record & Physical/Environment Requirements:

• Ability to travel 15 % travel, overnight, within USA and internationally
• Must have a valid driver’s license with an acceptable driving record
• Ability to lift, move or carry equipment up to 50lb
   

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

• Root Cause analysis and Risk mitigation Experience
• Minitab, and Microsoft Applications
• Identifying, analyzing and mitigating risk
• SAP or other related ERP experience
   

Cytiva, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it’s a hea