Supervisor Quality Release

Join a Dedicated Team in Life-Saving Technology

At our organization in Zurich, part of a leading medical device division, we design and manufacture life-saving heart pump systems that support patients with advanced heart failure globally. Our products, like CentriMag and HeartMate 3, are crafted with both technical excellence and a strong commitment to patient care.

We foster a collaborative environment with a focus on professional growth, and we are excited to welcome an individual who is passionate about leadership and continuous learning.

Role Overview

In this position, you will have the opportunity to lead a dedicated Quality Release team, ensuring that our products meet the highest standards of safety and compliance. Working across cross-functional teams including Manufacturing, Engineering, and Regulatory, you will utilize your technical knowledge and leadership abilities to drive improvements and enhance quality assurance processes.

Key Responsibilities

• People & Team Leadership:
  • Lead and support a diverse team of 5–10 colleagues, promoting an inclusive and collaborative culture.
  • Set clear, achievable goals aligned with departmental objectives.
  • Provide guidance, feedback, and career development opportunities for team members.
  • Oversee task allocation to ensure quality and compliance in deliverables.
• Product Release & Compliance:
  • Manage product release activities, ensuring products are safe and effective prior to market introduction.
  • Collaborate with stakeholders to review production and quality records.
  • Enhance adherence to GDP/GMP standards in documentation and release processes.
  • Serve as the final authority on product release decisions within your scope.
• Continuous Improvement & Projects:
  • Lead quality improvement initiatives aimed at enhancing efficiency and compliance.
  • Manage quality projects by developing plans and aligning with cross-functional objectives.
  • Support quality audits and inspections, taking responsibility for quality release outcomes.
• Collaboration & Communication:
  • Work closely with Operations, Engineering, and Supply Chain to address quality challenges effectively.
  • Represent the team in meetings and cross-functional forums.
  • Train and mentor Quality Release operators in processes and quality principles.

Qualifications & Experience

• Bachelor’s degree (or equivalent) in a relevant field.
• 4–6 years of experience in Quality or Quality Control within regulated environments.
• Demonstrated experience in people leadership, ideally with at least two years in a team-lead capacity.
• Familiarity with ISO 13485 and global medical device regulations is required.
• Experience with Class II or Class III medical devices is an advantage.
• Excellent communication and presentation skills, fluent in English; proficiency in German at B1 level or higher.

Why Join Us?

Joining our team means being part of a mission-driven organization that values collaboration, diversity, and personal growth. You can expect:

• Meaningful work that directly contributes to improving and saving lives.
• Opportunities for long-term career development in a global healthcare environment.
• A stable and resilient industry with a collaborative and skilled workforce.
• A modern workplace located in the vibrant heart of Zurich.
• A culture where diverse perspectives are appreciated and valued.

Your Next Step

If you are passionate about leading with purpose and contributing to impactful work, we encourage you to explore this exciting opportunity. We look forward to hearing from individuals who are eager to grow and make a difference.