Senior Quality Engineer

Danaher • Duncan, OK

5d • Onsite

About The Position

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 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. Learn about the Danaher Business System which makes everything possible. The Senior Quality Engineer is responsible for providing quality assurance services to ensure the integrity of products received and shipped out, services provided to clients, support business and customer needs, and comply with government regulations, industry and Cytiva standards. This position reports to the Sr Manager, Site Quality and is part of the quality team located in Duncan, SC and will be an on-site role.

Requirements

• Bachelor’s degree in engineering (e.g. Biomedical, Chemical, Pharma, Industrial, Mechanical, Systems, Quality, Reliability) or equivalent work experience.
• Experienced in managing quality workflows, including qualification, auditing, change management, CAPA resolution, deviations, and QMS development.
• Strong interpersonal and communication skills to implement and execute strategies that ensure compliance with regulatory and industry standards.

Nice To Haves

• Strong problem solving, and root-cause analysis skills with the ability to influence others to drive change (cross-functionally and globally).
• Experience with electronic QMS platforms (VEEVA, Magic) and SAP Inventory Management preferred.

Responsibilities

• Maintain and implement Standard Operating procedures, process flow charts, Process Control Plans, Process FMEA, change controls, and validations.
• Lead or support site level projects and initiatives ensuring Quality Assurance priorities are fully integrated in operational strategies, and regulatory compliance is maintained.
• Partner with cross-functional stakeholders to support expansion, risk mitigation and productivity while ensuring product quality.
• Manage Non-conformance, CAPA and Complaint processes; perform root cause analysis and implement robust corrective actions.
• Verify effectiveness to prevent recurrence and ensure timely closure.
• Provide manufacturing quality trend analysis and recommend improvements.
• Support Kaizen and Shin Kaizen events using Lean manufacturing principles, and Danaher Business System tools to drive continuous improvements.

Benefits

• Cytiva, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives.
• Whether it’s 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.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level