Finde einen Job 
Finde eine Ausbildung 
Top Arbeitgeber 
Top Universitäten 
Für Unternehmen 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: Full-time on-site role with opportunities for professional growth and development.
- Warum dieser Job: Make a real impact on product quality while collaborating with diverse teams in a dynamic environment.
- Gewünschte Qualifikationen: Bachelor's in Engineering or Life Sciences; experience in quality management and fluent in German and English.
- Andere Informationen: Must have the right to work in Tuttlingen; advanced degree preferred.
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.
#J-18808-Ljbffr
Quality Manager Arbeitgeber: Hobson Prior
Kontaktperson:
Hobson Prior 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 in your conversations. These are crucial for the role, and demonstrating your expertise can set you apart from other candidates.
✨Tip Number 2
Prepare to discuss specific examples of how you've improved quality management systems in previous roles. Use metrics and outcomes to showcase your impact on quality assurance.
✨Tip Number 3
Familiarize yourself with the latest trends and regulatory changes in the medical device industry. Being knowledgeable about current best practices will show your commitment to continuous improvement.
✨Tip Number 4
Emphasize your leadership skills and ability to collaborate with cross-functional teams. Quality management is a team effort, and showcasing your teamwork can make a strong impression.
Diese Fähigkeiten machen dich zur top Bewerber*in für die Stelle: Quality Manager
Tipps für deine Bewerbung 🫡
Understand the Role: Take the time to thoroughly read the job description for the Quality Manager position at Hobson Prior. Make sure you understand the key responsibilities and qualifications required, especially regarding ISO 13485 and regulatory compliance.
Tailor Your CV: Customize your CV to highlight your experience in quality management within the medical device industry. Emphasize your knowledge of ISO standards, FDA regulations, and any relevant achievements that demonstrate your leadership skills and commitment to quality.
Craft a Strong Cover Letter: Write a compelling cover letter that connects your background and skills to the specific requirements of the Quality Manager role. Mention your experience with developing Quality Management Systems and your ability to foster a culture of continuous improvement.
Proofread Your Application: Before submitting your application, carefully proofread your CV and cover letter for any errors or inconsistencies. Ensure that your documents are clear, professional, and free of typos, as attention to detail is crucial in quality management.
Wie du dich auf ein Vorstellungsgespräch bei Hobson Prior vorbereitest
✨Showcase Your Quality Management Expertise
Be prepared to discuss your experience with ISO 13485 and other relevant standards. Highlight specific examples of how you've developed and maintained Quality Management Systems in previous roles.
✨Demonstrate Leadership Skills
Since the role requires exceptional leadership, think of instances where you've led cross-functional teams or initiatives. Share how you fostered a culture of quality and continuous improvement in your past positions.
✨Prepare for Technical Questions
Expect questions related to regulatory compliance and quality assurance processes. Brush up on your knowledge of CE Mark requirements and FDA regulations to confidently answer any technical inquiries.
✨Communicate Effectively in Both Languages
As fluency in both German and English is required, practice discussing your qualifications and experiences in both languages. This will demonstrate your ability to communicate effectively in a bilingual environment.
