Senior Quality Engineer (Sunday-Thursday)

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 is responsible for ensuring the quality of membrane products and medical devices by facilitating cross-functional execution of the Quality Management System (QMS) setting inspection processes implementing quality control measures and identifying statistical trends. This role ensures compliance with ISO 13485 and ISO 9001 standards addresses customer complaints resolves production quality issues and supports new product introduction projects. Additionally the Senior Quality Engineer drives continuous improvement and collaborates with R&D manufacturing and regulatory teams to maintain product safety and regulatory compliance.

This position reports to the Senior Manager Site Quality and is part of the Quality Engineering group located in Pensacola and will be an on-site role is for working days of Sunday to Thursday.

What you will do:

• Provided strategic quality oversight for manufacturing operations ensuring compliance with applicable regulatory standards while driving a culture of quality excellence across production teams.
• Led complex root cause investigations and remediation efforts using tools such as 8D DMAIC and fishbone analysis implementing robust corrective and preventive actions to eliminate recurring issues.
• Directed process validation and control strategies (IQ/OQ/PQ SPC) improving process capability reducing variability and maintaining consistent product quality in high-volume manufacturing environments.
• Applied risk-based approaches (PFMEA control plans ISO 14971 principles) to proactively identify and mitigate process risks ensuring product safety reliability and compliance.
• Collaborated cross-functionally with engineering operations and suppliers to drive continuous improvement initiatives optimize manufacturing processes and support successful product transfers and launches.

Who you are:

• Bachelors degree in Engineering or related Science field.
• 5 years experience in quality engineering in a regulated environment
• Preferred experience in high volume manufacturing environments using lean principals
• Preferred green belt and/or CQE
• Strong knowledge of either ISO 9001/13485/16949 FDA QSR and risk management tools.

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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