Quality Manager (M-Th 4pm-3am 410's)

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 the Quality Manager (Night Shift) provides site-level quality leadership during off-shift manufacturing operations. This role ensures compliance to QMS regulatory and customer requirements while supporting uninterrupted operations real-time issue resolution and strong quality culture across night shift teams.

This position reports to the Sr Manager Site Quality that leads Quality on nights 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:

• Serve as the primary quality authority for night shift providing real-time decision making and escalation as required
• Ensure consistent application of QMS DBS/lean principles and site procedures during night shift activities
• Oversee nightshift investigations ensure evidencebased RCA and escalate systemic issues to site quality leadership
• Lead containment risk assessment and disposition decisions for deviations nonconformances batch documentation and material holds during offshift operations.
• Coach nightshift teams on quality ownership standard work and DBS problem solving; identify trends and drive improvements that prevent recurrence

Who you are:

• Hold a Bachelors degree preferably in Science Business or Engineering.
• Have at least 5 years of experience in Quality Assurance Quality Engineering or Manufacturing Operations within Life Sciences Biotechnology Medical Device Biopharma or other FDA/EPA-regulated manufacturing environments.
• Possess an additional 2 years of leadership experience in Operations Quality Engineering within a regulated industry.
• Leadership and Communication: Proven ability to lead coach and mentor teams; manage performance; plan succession; and effectively communicate at all organizational levels both written and verbal.
• Willing to go to Gemba

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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