Manager Quality Compliance & Release

Reposted 9 Days Ago
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Hoegaarden, BEL
In-Office
Senior level
Biotech
The Role
The Manager of Quality Compliance & Release leads the compliance and release group, overseeing quality systems, product release, and managing audits and compliance metrics.
Summary Generated by Built In

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 Manager Quality, Compliance & Release (QCR) is responsible for leading the compliance and release group, providing coaching and direction to the local Compliance Officers and Quality Specialists.

This position reports to the Sr Manager, Site Quality and is part of the Quality Department  located in Hoegaarden, Belgium and will be an on-site role. 

What you will do:

  • You will be managing the Customer Audits, heading Quality Systems related activities and be responsible for the local Quality System in our global document management system.
  • You will be responsible for final product release to market.
  • Your main areas of responsibility are divided in approximately 10% customer audits and 50% Quality Systems activities and 40% product Release activities.
  • The Manager QCR is keeping oversight of quality compliance activities (internal and external) and managing the metrics and KPI related to this.
  • The Manager QCR is maintaining the overview of the certified state of products
  • The Manager QCR is the Quality Lead responsible in plant-wide continuous improvement projects related to QA Compliance and Release.

#LI-KS1

Who you are:

  • Able to teach, coach & guide associates; you master situational leadership. Can deal with change and is able to guide others through change (ADKAR)
  • good communicator, able to choose suitable communication means & moments
  • likes to interact with shopfloor (GEMBA) and facilitates conversation and decision making based on data and risk-based approach
  • 5 plus years of quality experience, experience (in a manufacturing environment) as a people leader. strong working knowledge of quality assurance principles and practices, industry and international regulations and standards
  • Fluency in English and Dutch is required (written & spoken)

Travel, Motor Vehicle Record & Physical/Environment Requirements:

  • Ability to travel (international) – 5-10% max
  • Must have a valid driver’s license

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 www.danaher.com.

Skills Required

  • 5 plus years of quality experience
  • Experience in a manufacturing environment as a people leader
  • Strong working knowledge of quality assurance principles and practices
  • Fluency in English and Dutch

Cepheid Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Cepheid and has not been reviewed or approved by Cepheid.

  • Leave & Time Off Breadth PTO and paid holidays are portrayed as robust, with formal programs and mentions of generous time off and rollover in some cases. This breadth supports a positive view of time-off availability.
  • Healthcare Strength Core medical, dental, and vision coverage is highlighted repeatedly and is viewed as comprehensive for regular full‑time employees. Descriptions such as “good” or “great” benefits reinforce the strength of the health coverage.
  • Retirement Support A 401(k) plan with company matching is consistently included as part of the package. The presence of matching contributions strengthens perceived retirement readiness.

Cepheid Insights

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The Company
HQ: Sunnyvale, CA
4,883 Employees
Year Founded: 1996

What We Do

Cepheid is dedicated to improving healthcare by pioneering molecular diagnostics that combine speed, accuracy, and flexibility. The company's GeneXpert® systems and Xpert® tests automate highly complex and time-consuming manual procedures, providing A Better Way for institutions of any size to perform world-class PCR testing. Cepheid’s broad test portfolio spans respiratory infections, blood virology, women’s and sexual health, TB and emerging infectious diseases, healthcare-associated infectious diseases, oncology and human genetics. The company’s solutions deliver actionable results where they are needed most – from central laboratories and hospitals to near-patient settings. For more information, visit http://www.cepheid.com.

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