Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That`s why we are always looking for curious minds that see themselves imagining the unimageable with us.
Your Role
Own end-to-end quality management for the Associate Manager, Quality role within the Life Science division, ensuring compliance with ISO, GMP, and applicable regulatory standards.
Lead cross-functional teams to embed quality practices throughout the product lifecycle and drive continuous improvement.
Establish KPI-driven dashboards to monitor quality performance and progress toward strategic objectives.
Maintain accountability for audit readiness, third-party certifications, and robust documentation practices.
Collaborate with manufacturing and supply chain to conduct risk assessments and perform root cause analysis on customer complaints and non-conformances.
Implement robust CAPA processes to prevent recurrence and drive corrective actions across functions.
Coordinate Factory Acceptance Tests (FAT) with customers and ensure complete documentation packages for final product delivery.
Promote a culture of safety, sustainability, and operational excellence while mentoring the team and aligning goals with the broader organizational mission.
Lead end-to-end product quality releases and ensure products meet the organization’s quality standards
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You bring 8 or more years of experience in quality assurance or quality systems within regulated manufacturing environments, supported by a degree in Mechanical Engineering, Instrumentation Engineering, or related discipline.
You have solid working knowledge of GMP and ISO standards, with hands-on experience managing quality management systems, document control workflows, and regulated deliverables across the product lifecycle.
You hold a Lean Six Sigma Green Belt certification (Black Belt preferred) and have applied structured methodologies to drive measurable process improvements in manufacturing or packaging operations.
You demonstrate proven capability in CAPA management, root cause analysis, non-conformance handling, and validation activities including IQ, OQ, and PQ with an understanding of CSV concepts.
You have experience preparing for and managing external audits, inspections, and third-party certifications, as well as coordinating with customers during Factory Acceptance Tests.
You are an effective communicator and cross-functional collaborator, with the ability to mentor and develop team members while aligning quality goals with broader organizational objectives.
You bring a proactive approach to EHS compliance and sustainability, promoting a culture of safety, accountability, and continuous improvement within your team.
What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging those impacts millions and empowers everyone to work their magic and champion human progress!
Apply now and become a part of our diverse team!
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