Quality Engineering Manager

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 who care for each other our customers and their patients. Take your next step to an altogether life-changing career.

Learn about theDanaher Business System which makes everything possible.

As theQuality Engineering Manageryou will collaborate closely with cross functional leadership and associates to ensure compliant execution monitoring and continuous improvement. You will also provide support for new product introduction process improvements and defect reductions.

This position reports to the Senior Manager Site Quality and leads the Quality Engineering team located in Pensacola Florida. This is an on-site role. At Cytiva our vision is to advance future therapeutics from discovery to delivery.

What you will do:

• Serves as the accountable owner for assigned quality events CAPAs and PSPs by owning decisionmaking risk assessment coordination escalation and closure while appropriately delegating execution tasks to responsible functions without relinquishing overall accountability.
• Lead and manage Complaint Defect Tracking and Resolution (CDT&R) for products. Tasks include analyzing trends tracking major issues and related corrective actions triaging coordinating and supporting investigations writing and reviewing technical reports for customer and interfacing with customers in various forms of communications.
• Provide guidance to other cross-functional departments on Containment Actions Root Cause Analysis Investigation Activities and Corrective Action Plans for internal non-conformances. Review and approve Investigations and CAPAs owned by other departments
• Apply DBS problemsolving methodologiesincluding root cause analysis standard work daily management Six Sigma and Lean principlesto resolve quality challenges and prevent recurrence.
• Leverage statistical analysis and data visualization in Microsoft Excel to guide quality engineering decisions support investigations and drive continuous improvement in a regulated manufacturing environment.
• Team Development & Performance: Build a high-performing quality Engineering department fostering a safe empowering environment that encourages skill development psychological safety and continuous improvement.
• Provide quality engineering leadership with expertise in ISO 13485 compliance statistical sampling strategies gage R&R validation (IQ/OQ/PQ) cleanroom environments and DOE to support riskbased datadriven decisionmaking.

Who you are:

• Bachelors degree in Engineering Science or a related technical discipline.
• 5 years of experience in Quality Engineering Quality Assurance or related quality roles within a regulated industry.
• 2 years of people leadership or demonstrated experience leading crossfunctional teams.
• Strong working knowledge of ISO 9001 and/or ISO 13485 GMP principles and QMS requirements.
• Ability to lead coach and mentor teams through collaboration & influence; strong written and verbal communication across all organizational levels.
• Demonstrated expertise in investigations CAPA risk management and change control.
• Analytical & Process Optimization: Skilled in statistical quality methods Lean principles Six Sigma and Root Cause Analysis for data-driven decision-making and embracing AI. Motivated eager and excited to make a difference.

Travel Motor Vehicle Record & Physical/Environment Requirements:

• Ability to travel 10% of the time to other Cytiva manufacturing locations in the US and Worldwide as required.
• Ability to access gauges and equipment 5-6 feet off the ground lift and move 20-35 lb. parcels.

It Would Be a Plus If You Also Possess Previous Experience In

• Contamination control sterilization sanitation or E-beam processes including ISO 14644 cleanroom operations.
• Enterprise systems such as SAP Oracle Veeva or Magic supporting laboratory or quality operations.

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 atDanaher Benefits Info.

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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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.

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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 .