Quality Excellence 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 Excellence Leaderyou will collaborate closely with cross functional leadership and associates to ensure compliant execution monitoring and continuous improvement of the implemented QMS in line with certification requirements and customer expectations.

This position reports to the Quality Director Filtration Membrane Sites and leads the Quality team located in Hauppauge New York. This is an on-site role. At Cytiva our vision is to advance future therapeutics from discovery to delivery.

What you will do:

• Quality Leadership & Compliance: Serve as the sites Quality Management Representative leading QA/QC functions ensuring regulatory compliance and aligning with organizational quality goals.
• Quality Management System (QMS): Implement maintain and optimize the Cytiva QMS ensuring procedures work instructions and IT systems support site operations and drive continuous improvement.
• Strategic Partnership & Advocacy: Collaborate with site and global leadership to address process changes advocate for site-specific needs and drive customer-centric solutions during change management initiatives.
• Team Development & Performance: Build a high-performing quality department fostering a safe empowering environment that encourages skill development psychological safety and continuous improvement.
• Audits Reporting & Representation: Lead Quality Management Reviews define and monitor KPIs host audits and represent the site in executive discussions and global best practice initiatives.

Who you are:

• Hold a Bachelors degree in Science preference in Chemistry or Engineering (or equivalent professional experience).
• Have at least 5 years in Quality Assurance or Quality/Process Engineering within FDA/EPA-regulated environments (Life Sciences Biotechnology Medical Device Biopharma). Including 2 years in validation and FMEA methodologies. Experience with contamination control cleanroom operations environmental monitoring and microbiology preferred.
• Prior leadership experience preferred. Ability to lead coach and mentor teams through collaboration & influence; strong written and verbal communication across all organizational levels.
• Regulatory & Quality Expertise: Knowledge of ISO 9001/13485 standards FDA regulations cGMPs CFR requirements and quality systems (CAPA complaints change control audits risk management).
• Analytical & Process Optimization: Skilled in statistical quality methods Lean principles Six Sigma and Root Cause Analysis for data-driven decision-making.
• Strategic & Operational Acumen: Capacity to manage budgets evaluate opportunity costs and drive innovative problem-solving while maintaining exceptional organizational and time management skills.
• 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.

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.

The annual salary range for this role is $120000 - $140000. This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting. This range may be modified in the future.

This job is also eligible for bonus/incentive pay.

We offer comprehensive package of benefits including paid time off medical/dental/vision insurance and 401(k) to eligible employees.

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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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- or .