Senior Quality Engineer- Projects

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 Danahers 15 operating companies our work saves livesand were all united by a shared commitment to innovate for tangible impact.

Youll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danahers 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 Senior Quality Engineer- Projects plays a critical role in supporting high-impact customer-facing initiatives. This role partners closely with cross-functional teams to ensure projects are executed compliantly risks are proactively mitigated and sustainable solutions are implemented using data-driven quality engineering practices. The position is hands-on highly collaborative and essential to driving consistent execution and a strong quality culture across the site.

This position reports to the Sr. Manager Quality Engineering Projects and is part of the Membrane- Filtration Team located in Pensacola FL and will be an on-site role.

What you will do:

• Support execution of highimpact crossfunctional priority quality engineering projects ensuring compliant delivery aligned with QMS regulatory and customer requirements.
• Apply structured problem solving (RCA CAPA risk assessments statistical analysis) to identify root causes and implement sustainable solutions.
• Partner with Manufacturing Engineering Supply Chain R&D and Regulatory teams to drive quality delivery and risk mitigation outcomes.
• Analyze quality and process data to identify trends support decisionmaking and demonstrate project effectiveness through defined KPIs.
• Support audit readiness and execution (internal external regulatory and customer) related to quality engineering initiatives.

Who you are:

• Bachelors degree in Engineering or science; or 5 years engineering experience.
• Additional 35 years of experience in Quality Engineering or Manufacturing Engineering within an ISO 13485 or highly regulated environment.
• Able to apply knowledge of QMS ISO 9001 ISO 13485 FDA/cGMP requirements into riskbased thinking writing controlled documents change control and performing quality event investigations.
• Are proficient in Lean Six Sigma SPC MSA and Gage R&R methodologies.
• Collaborative analytical innovative and executionfocused with the ability to influence across functions and communicate clearly at all levels. Disciplined accountable willing & eager to make a difference!

Travel Motor Vehicle Record & Physical/Environment Requirements: if applicable for role

• Ability to travel 15 % travel overnight within USA and internationally
• Must have a valid drivers 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:

• Have experience in filtration membranes or bioprocessing manufacturing environments.
• Bring exposure to analytical chemistry microbiology contamination control sterilization or ISO 17025 environments.
• Have used systems such as SAP Veeva Magic or Oracle.

Cytiva a Danaher operating company offers a broad array of comprehensive competitive benefit programs that add value to our lives. Whether its a health care program or paid time off our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info.

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 Companys sole discretion unless and until paid and may be modified at the Companys sole discretion consistent with the law.

Join our winning team today. Together well accelerate the real-life impact of tomorrows 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.

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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- or .