Auf einen Blick
- 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 assurance, mastery of ISO standards, and strong problem-solving skills required.
- Andere Informationen: Must be autonomous and possess good English communication skills.
Das voraussichtliche Gehalt liegt zwischen 48000 - 72000 € pro Jahr.
You can find all our offers on our Career site by clicking here : Supplier Quality Engineer 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
Make sure to 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 with supplier management processes 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 experience needed for the role.
✨Tip Number 3
Brush up on your knowledge of quality tools like 5P, 5M, and 8D. Being able to reference these tools and explain how you've used them in previous roles can set you apart from other candidates.
✨Tip Number 4
Prepare to discuss your approach to continuous improvement and problem-solving. Think of specific projects where you've led initiatives or contributed to quality improvements, as this aligns well with the responsibilities of the position.
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, as this will help you tailor your application.
Highlight Relevant Experience: In your CV and cover letter, emphasize your experience in quality management within the pharmaceutical or medical device industry. Be specific about your roles in supplier management, audits, and quality improvement projects.
Showcase Your Skills: Make sure to mention your mastery of ISO 9001 & 13485 standards, as well as your knowledge of quality tools and risk analysis methods. Provide examples of how you've applied these skills in previous roles.
Craft a Strong Cover Letter: Write a compelling cover letter that connects your background to the job requirements. Discuss your autonomous work style, team spirit, and how you can contribute to continuous quality improvement at the company.
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 addressed quality issues in the past. Use the 8D methodology or similar tools to illustrate your approach.
✨Understand Supplier Management
Familiarize yourself with supplier management processes and be ready to discuss how you would maintain effective relationships with suppliers. Mention any experience you have with audits and evaluations.
✨Communicate Effectively
As internal communication is key in this role, practice articulating your thoughts clearly. Be ready to explain how you would feed back information from various departments within the Quality Department.