At a Glance
- Tasks: Lead quality assurance across multiple sites and strengthen the Quality Management System.
- Company: Established medical-device manufacturer with a focus on innovation and quality.
- Benefits: Competitive salary, career growth opportunities, and a chance to make a real impact.
- Other info: Be part of a strategic team during exciting regulatory changes and audits.
- Why this job: Join a pivotal growth phase and drive quality culture in a dynamic environment.
- Qualifications: Experience in QA management, ISO 13485 knowledge, and CAPA expertise.
Meet Life Sciences is partnering with an established medical-device manufacturer to recruit an experienced QA Manager. You will lead quality across multi-site operations, strengthen the QMS, and support regulatory submissions.
The role requires hands-on leadership, robust ISO 13485 knowledge, CAPA mastery, and the ability to drive a practical quality culture across teams.
This is a strategic hire during a pivotal growth phase with MDR readiness and ongoing audits on the horizon.
#J-18808-LjbffrQuality Assurance Manager - ISO 13485 & MDR Readiness employer: Meet Life Sciences
As a Market Access Consultant with our client, you will be part of a dynamic team that values innovation and collaboration in the evolving healthcare landscape. The company offers a supportive work culture with opportunities for professional growth, including mentoring junior team members and leading impactful projects. With competitive compensation, hybrid working options, and comprehensive benefits, this role provides a meaningful opportunity to contribute to the expansion of European Value & Access capabilities while enjoying a fulfilling work-life balance.
