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 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.

What you will do:

• Lead Quality Investigations: Lead and support investigations related to manufacturing deviations nonconformances out-of-specification events and customer complaints ensuring timely resolution thorough root cause analysis and high-quality documentation in compliance with QMS and regulatory requirements.

• Analyze Quality Data and Drive Improvements: Monitor and analyze quality metrics trends and process performance data; identify recurring issues support risk assessments and drive corrective and preventive actions (CAPAs) to improve product quality and operational effectiveness.

• Cross-Functional Collaboration: Partner with Manufacturing Operations R&D Supply Chain and Quality teams to support investigations process validations change controls and continuous improvement initiatives; author and review technical reports investigation records and quality documentation.

• Support Compliance and Continuous Improvement: Serve as a quality engineering resource during internal and external audits regulatory inspections and customer visits; contribute to QMS enhancements and lead projects that strengthen compliance reduce risk and improve manufacturing performance.

Who you are:

• Education & Experience: Bachelors degree in Engineering Life Sciences or a related technical discipline or equivalent industry experience (minimum 5 years) in a GMP-regulated environment such as biopharmaceutical biotechnology medical device or pharmaceutical manufacturing; at least 3 years of experience supporting investigations CAPA and quality systems activities.

• Technical & Regulatory Expertise:Strong knowledge of cGMP ISO 9001/13485 and core QMS principles; experienced in audit readiness documentation practices and driving QMS improvements across cross-functional teams.

• Communication & Problem Solving: Demonstrated ability to manage multiple priorities in a fast-paced manufacturing environment; skilled in technical writing data analysis root cause investigation methodologies and cross-functional collaboration with a strong attention to detail and commitment to quality.

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.

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.

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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 .