My client seeks an experienced Quality Manager to elevate quality standards in the medical device industry. As a leader in a dynamic, international environment, you’ll play a pivotal role in ensuring product excellence, regulatory compliance, and continuous improvement in quality systems.

Why You Should Apply:

• Join a global company with cutting-edge impact in medical devices.
• Drive quality assurance systems and maintain compliance with top industry standards.
• Lead a talented team focused on quality, innovation, and operational excellence.
• Opportunity to revitalize a department and make a lasting impact on the organization.
• Competitive compensation and comprehensive benefits package.

What You’ll Be Doing:

• Developing, implementing, and refining Operational Quality Systems to meet regulatory and internal standards.
• Leading and mentoring the Quality Engineering team, setting key metrics and goals.
• Acting as the technical expert for quality compliance, audits, and supplier controls.
• Conducting internal and external audits to ensure compliance with quality standards.
• Engaging in supplier and customer surveys for compliance and quality assurance.

About You:

• Be able to do the job as described.
• Mastery of ISO 13485 and FDA 21 CFR Part 820 regulations.
• Certified Quality Auditor or Manager preferred, with Six Sigma Green or Black Belt.
• Strong communicator, adaptable, and proactive team player.
• Ability to travel up to 30%.

How To Apply:

We’d love to see your resume, but we don’t need it to have a conversation. Send an email to ccupo@jacobsmgt.com and tell me why you’re interested. Or, if you do have a resume ready, apply here.