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- Aufgaben: Manage supplier relationships and ensure quality standards are met.
- Arbeitgeber: Join a leading company in the pharmaceutical and medical device industry.
- Mitarbeitervorteile: Enjoy a collaborative work environment with opportunities for continuous improvement.
- Warum dieser Job: Make a real impact on product quality and safety while working with diverse teams.
- Gewünschte Qualifikationen: 5+ years in quality, mastery of ISO standards, and strong problem-solving skills required.
- Andere Informationen: Must be autonomous and have a good command of English.
Das voraussichtliche Gehalt liegt zwischen 60000 - 84000 € pro Jahr.
You can find all our offers on our Career site by clicking here :
Main Activities
- Supplier Management: Maintain and implement supplier management processes to ensure strong and effective relationships.
- Selection and Evaluation: Participate in the selection, qualification and periodic evaluation of suppliers according to established procedures.
- Complaints and Notifications: Ensure the processing and follow-up of supplier complaints and change notifications within the required timeframes.
- Assessment Meetings: Organize and participate in change impact assessment meetings.
- Audits: Plan, organize and carry out supplier and distributor audits.
- Quality: Handle quality events (non-conformity, OOS, change control, CAPA) in collaboration with other departments.
- Continuous Improvement: Lead problem-solving groups and support continuous quality improvement projects.
- Internal Communication: Feed back information from the various departments within the Quality Department.
- Quality Referent: Intervene on projects as a quality referent, review new design specifications and provide your input on component quality and manufacturing feasibility.
- Investigations and Corrective Actions: Investigate supplier material failures and develop corrective action plans if necessary.
- Acceptance Criteria: Develop material acceptance criteria and activities.
Profile
- Mastery of Quality Standards ISO 9001 & 13485
- Knowledge of MDR
- Certified Lead Auditor 13485
- Knowledge of Quality tools (5P, 5M, 8D,…) and risk analysis methods
- English: Good comprehension and writing skills (minimum level B2)
- Basic training: CFC or equivalent
- Professional experience required: Minimum 5 years of experience in quality in the pharmaceutical and/or medical device industry
- Autonomous, rigorous, with a strong team spirit
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Senior Supplier Quality Engineer Arbeitgeber: Teoxane SA
Kontaktperson:
Teoxane SA HR Team
StudySmarter Bewerbungstipps 🤫
So bekommst du den Job: Senior Supplier Quality Engineer
✨Tip Number 1
Familiarize yourself with the specific quality standards mentioned in the job description, such as ISO 9001 and 13485. Being able to discuss these standards confidently during your interview will demonstrate your expertise and commitment to quality.
✨Tip Number 2
Highlight your experience in supplier management and audits. Prepare examples of how you've successfully managed supplier relationships or conducted audits in the past, as this will show that you have the practical skills needed for the role.
✨Tip Number 3
Brush up on your knowledge of quality tools like 5P, 5M, and 8D. Be ready to discuss how you've applied these tools in real-world scenarios to solve problems and improve quality processes.
✨Tip Number 4
Since the role requires good English comprehension and writing skills, practice articulating your thoughts clearly in English. This will help you communicate effectively during interviews and demonstrate your language proficiency.
Diese Fähigkeiten machen dich zur top Bewerber*in für die Stelle: Senior Supplier Quality Engineer
Tipps für deine Bewerbung 🫡
Understand the Role: Take the time to thoroughly read the job description for the Senior Supplier Quality Engineer position. Make sure you understand the key responsibilities and required qualifications, such as mastery of ISO 9001 & 13485 standards.
Tailor Your CV: Customize your CV to highlight relevant experience in supplier management, quality assurance, and any specific tools or methodologies mentioned in the job description, like 5P, 5M, or 8D.
Craft a Strong Cover Letter: Write a cover letter that connects your professional background with the requirements of the role. Emphasize your experience in the pharmaceutical or medical device industry and your ability to lead continuous improvement projects.
Highlight Language Skills: Since good comprehension and writing skills in English are required, make sure to mention any relevant language certifications or experiences that demonstrate your proficiency at a minimum B2 level.
Wie du dich auf ein Vorstellungsgespräch bei Teoxane SA vorbereitest
✨Showcase Your Experience
Be prepared to discuss your previous roles in quality management, especially in the pharmaceutical or medical device industry. Highlight specific projects where you implemented quality standards like ISO 9001 & 13485.
✨Demonstrate Problem-Solving Skills
Since the role involves leading problem-solving groups, come equipped with examples of how you've successfully tackled quality issues in the past. Use the STAR method (Situation, Task, Action, Result) to structure your responses.
✨Familiarize Yourself with Quality Tools
Brush up on quality tools and risk analysis methods such as 5P, 5M, and 8D. Be ready to discuss how you've applied these tools in your previous work to improve processes and outcomes.
✨Prepare for Technical Questions
Expect technical questions related to supplier management and audits. Review the key aspects of supplier evaluation and change impact assessments, and be ready to explain your approach to these processes.
