Quality Manager

Quality Manager

Tuttlingen Vollzeit 43200 - 72000 € / Jahr (geschätzt) Kein Home Office möglich
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Auf einen Blick

  • Aufgaben: Lead quality management for medical devices, ensuring compliance and continuous improvement.
  • Arbeitgeber: Join Hobson Prior, a leader in the medical device industry focused on quality and safety.
  • Mitarbeitervorteile: Work full-time on-site with opportunities for professional growth and development.
  • Warum dieser Job: Be part of a culture that values quality and innovation while making a real impact.
  • Gewünschte Qualifikationen: Bachelor's degree in Engineering or Life Sciences; experience in quality management required.
  • Andere Informationen: Fluency in German and English is essential; must work on-site in Tuttlingen.

Das voraussichtliche Gehalt liegt zwischen 43200 - 72000 € pro Jahr.

Hobson Prior is seeking a highly skilled and experienced Quality Manager to join their team. The Quality Manager will be responsible for ensuring that all products meet the highest standards of quality, safety, and regulatory compliance. This role requires a deep understanding of quality management systems, regulatory requirements, and industry standards specific to medical devices. The ideal candidate will have a strong background in quality assurance, exceptional leadership skills, and a commitment to continuous improvement.

Please note that to be considered for this role you must have the right to work in this location.

Responsibilities:

  • Develop and maintain the Quality Management System (QMS) in accordance with ISO 13485 and MDSAP.
  • Ensure compliance with all applicable regulatory requirements, including CE Mark and other international regulations.
  • Conduct regular audits, inspections, and reviews of production processes to identify areas for improvement and ensure compliance with quality standards.
  • Collaborate with cross-functional teams, including R&D, manufacturing, and supply chain, to develop and implement quality improvement initiatives.
  • Oversee the investigation and resolution of product quality issues, including non-conformances, CAPAs, and customer complaints.
  • Develop and maintain quality documentation, including standard operating procedures (SOPs), work instructions, and quality records.
  • Monitor and analyze key quality metrics, generating reports and presenting findings to senior management.
  • Stay up-to-date with industry trends, best practices, and regulatory changes to ensure continuous improvement and compliance.
  • Foster a culture of quality and continuous improvement throughout the organization.

Qualifications and Requirements:

  • Bachelor’s degree in Engineering, Life Sciences, or a related field; advanced degree preferred.
  • Experience in quality management within the medical device industry.
  • In-depth knowledge of ISO 13485, FDA regulations, CE Mark requirements, and other relevant standards.
  • Proven experience in developing and implementing Quality Management Systems (QMS).
  • Fluent in German and English.
  • Required to work full-time on-site in Tuttlingen.

Apply now

If you are interested in learning more or applying to this exciting opportunity, please click ‚Apply‘ and upload a copy of your CV.

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Quality Manager Arbeitgeber: Hobson Prior International Ltd

At Hobson Prior, we pride ourselves on being an exceptional employer that values quality and innovation in the medical device industry. Our collaborative work culture fosters continuous improvement and professional growth, providing employees with opportunities to develop their skills while making a meaningful impact on patient safety. Located in Tuttlingen, a hub for medical technology, we offer a dynamic environment where your expertise as a Quality Manager will be recognized and rewarded.
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Kontaktperson:

Hobson Prior International Ltd HR Team

StudySmarter Bewerbungstipps 🤫

So bekommst du den Job: Quality Manager

✨Tip Number 1

Make sure to highlight your experience with ISO 13485 and MDSAP during the interview. Be prepared to discuss specific examples of how you've developed and maintained Quality Management Systems in previous roles.

✨Tip Number 2

Familiarize yourself with the latest regulatory requirements and industry standards related to medical devices. This knowledge will not only help you answer questions confidently but also demonstrate your commitment to continuous improvement.

✨Tip Number 3

Prepare to discuss your leadership style and how you've successfully collaborated with cross-functional teams in the past. Sharing specific instances where you've led quality improvement initiatives can set you apart from other candidates.

✨Tip Number 4

Stay updated on industry trends and best practices by following relevant publications and attending webinars. This will not only enhance your knowledge but also show your proactive approach to quality management during the interview.

Diese Fähigkeiten machen dich zur top Bewerber*in für die Stelle: Quality Manager

Quality Management Systems (QMS)
ISO 13485
MDSAP
Regulatory Compliance
CE Mark Requirements
FDA Regulations
Quality Assurance
Leadership Skills
Continuous Improvement
Auditing and Inspection
Cross-Functional Collaboration
Root Cause Analysis
Corrective and Preventive Actions (CAPA)
Standard Operating Procedures (SOPs)
Data Analysis and Reporting
Fluency in German and English

Tipps für deine Bewerbung 🫡

Understand the Role: Before applying, make sure you fully understand the responsibilities and qualifications required for the Quality Manager position. Familiarize yourself with ISO 13485, FDA regulations, and CE Mark requirements as these are crucial for the role.

Tailor Your CV: Customize your CV to highlight your experience in quality management within the medical device industry. Emphasize your knowledge of quality management systems and any relevant certifications or training you have completed.

Craft a Strong Cover Letter: Write a compelling cover letter that showcases your leadership skills and commitment to continuous improvement. Mention specific examples of how you've successfully implemented quality initiatives in previous roles.

Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any errors or inconsistencies. Ensure that your application is clear, professional, and free of typos to make a great first impression.

Wie du dich auf ein Vorstellungsgespräch bei Hobson Prior International Ltd vorbereitest

✨Showcase Your Quality Management Expertise

Be prepared to discuss your experience with quality management systems, particularly ISO 13485 and MDSAP. Highlight specific examples where you've successfully implemented these standards in previous roles.

✨Demonstrate Leadership Skills

As a Quality Manager, leadership is key. Share instances where you've led cross-functional teams or initiatives that improved quality outcomes. This will show your ability to foster collaboration and drive change.

✨Prepare for Regulatory Questions

Expect questions about regulatory compliance, including CE Mark and FDA regulations. Brush up on these topics and be ready to explain how you've ensured compliance in past projects.

✨Emphasize Continuous Improvement

Discuss your commitment to continuous improvement by providing examples of how you've identified areas for enhancement in quality processes. This will demonstrate your proactive approach to quality management.

Quality Manager
Hobson Prior International Ltd
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