[29/09/2025] QA Specialist
3 weeks ago
Job Description
Bring more to life.
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology
At Beckman Coulter Diagnostics, one of 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.
As a global leader in clinical diagnostics, Beckman Coulter Diagnostics has challenged convention to elevate the diagnostic laboratory's role in improving patient health for more than 90 years. Our diagnostic solutions are used in routine and complex clinical testing, and are used in hospitals, reference and research laboratories, and physician offices around the world. Every hour around the world, more than one million tests are run on Beckman Coulter Diagnostics systems, impacting 1.2 billion patients and more than three million clinicians per year. From uncovering the next clinical breakthrough, to rapid and reliable sample analysis, to more rigorous decision making-we are enabling clinicians to deliver the best possible care to their patients with improved efficiency, clinical confidence, adaptive collaboration, and accelerated intelligence.
Learn about the which makes everything possible.
The Senior Manufacturing Quality Engineer for Beckman Coulter Diagnostics is responsible for:
- Provide Quality and Compliance expertise for system compliance, authoring, and reviewing end to end Design deliverables.
- Prepare documentation adhering to product development, Software Development Life Cycle processes, and regulatory requirements.
- Collaborate with teams guidance to project teams on implementing and adhering to quality standards.
- Maintain and develop IDC quality systems and infrastructure, and to monitor QMS performance and drive its fulfillment.
- Ensure compliance with organizational policies and regulatory requirements, including FDA, ISO 13485, and ISO 14971, with knowledge of IVDR.
- Send daily status reports to management, highlighting any risks.
- Support audits by liaising with management and qualify software for validation labs in conjunction with FSCs.
This position is part of the located at and will be on-site. At Beckman Coulter, our mission is to Relentlessly Reimagine Healthcare, One Diagnosis at a Time.
You will be a part of the Quality, Regulatory and Clinical Affairs and report to the Senior Manager Quality and Regulatory Affairs. If you thrive in a multifunctional role and want to work to build a world-class Quality organization-read on.
In this role, you will have the opportunity to:
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The essential requirements of the job include:
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It would be a plus if you also possess previous experience in:
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Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's 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.
For more information, visit .
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