Senior Quality Engineer

Senior Quality EngineerAre you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?At Cytiva, one of Danaher's 15+ operating companies, our work saves lives—and we're all united by a shared commitment to innovate for tangible impact.You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's 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.The Senior Quality Engineer is responsible for supporting manufacturing quality processes by monitoring production performance, analyzing quality data, assisting with root cause investigations, and implementing corrective actions to ensure products meet customer specifications and regulatory requirements while driving continuous improvement.This role partners closely with Operations, Manufacturing Engineering, Regulatory, Supply Chain, and site leadership to drive quality excellence, ensure compliance with internal and external requirements, and sustainably reduce quality risk.The position is a part of the quality engineering group, and provides support for deviations, investigations, CAPA, change management, and process improvement initiatives across the site.This position reports to the Quality Engineering Manager and is part of the Quality Assurance Department located in Pensacola, FL and will be an on-site role.What you will do:Analyzed quality and production data to identify trends, monitor key performance indicators (KPIs), and implement data-driven improvements that reduced defects and increased operational efficiency using lean principles.Conduct root cause investigations using structured problem-solving methodologies (CAPA, 8D, Fishbone, and 5 Whys) to resolve quality issues and prevent recurrence.Monitor shop floor processes to ensure compliance with specifications, control plans, and standard work instructionsParticipate in internal audits, layered process audits (LPA), and support external/customer audits while maintaining accurate quality documentation (e.g., SOPs, inspection records)Serve as the primary quality liaison between Manufacturing, Engineering, Supply Chain, and Customers, ensuring effective resolution of quality concerns and successful product deliveryWho you are:Bachelor's degree in engineering, science, or related technical discipline (preferred).5+ years of experience in Quality Engineering or Quality Systems within a regulated manufacturing environment.A detail-oriented and analytical problem solver with a strong interest in manufacturing quality and continuous improvementExperience with contamination control, sterility assurance, and quality systems utilizing SPC and Lean methodologies (Green Belt and/or CQE certification a plus); and/or experience in material science within regulated life sciences environments, including knowledge of applicable regulatory requirements.Comfortable working in a fast-paced production environment and collaborating with cross-functional teamsTravel, Motor Vehicle Record & Physical/Environment Requirements:Ability to lift, move or carry equipment up to 50lbIt would be a plus if you also possess previous experience in:Experience in life sciences, biotech, pharmaceutical, or medical device manufacturing.Familiarity with global regulatory expectations (e.g., FDA, ISO, GMP).Lean, Six Sigma, or similar continuous improvement certification.