Auf einen Blick
- Aufgaben: Manage supplier relationships, conduct audits, and lead quality improvement projects.
- Arbeitgeber: Join a leading company in the pharmaceutical and medical device industry.
- Mitarbeitervorteile: Enjoy a collaborative work environment with opportunities for professional growth.
- Warum dieser Job: Make a real impact on product quality and safety while working with diverse teams.
- Gewünschte Qualifikationen: 5+ years in quality assurance, knowledge of ISO standards, and strong English skills required.
- Andere Informationen: Ideal for autonomous individuals who thrive in a rigorous team setting.
Das voraussichtliche Gehalt liegt zwischen 48000 - 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 #J-18808-Ljbffr
Senior Supplier Quality Engineer Arbeitgeber: Whatjobs

Kontaktperson:
Whatjobs 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 can hit the ground running in this role.
✨Tip Number 3
Brush up on your knowledge of quality tools like 5P, 5M, and 8D. Being able to articulate how you've used these tools in previous roles will set you apart from other candidates and showcase your problem-solving skills.
✨Tip Number 4
Since internal communication is key in this role, think of ways you've effectively communicated across departments in your past experiences. Be ready to share specific instances where your communication skills led to successful outcomes.
Diese Fähigkeiten machen dich zur top Bewerber*in für die Stelle: Senior Supplier Quality Engineer
Tipps für deine Bewerbung 🫡
Understand the Role: Make sure to thoroughly read the job description for the Senior Supplier Quality Engineer position. Understand the key responsibilities and required qualifications, especially regarding quality standards like ISO 9001 & 13485.
Highlight Relevant Experience: In your CV and cover letter, emphasize your professional experience in quality within the pharmaceutical and/or medical device industry. Mention specific projects or roles where you demonstrated your mastery of quality tools and standards.
Showcase Problem-Solving Skills: Since the role involves leading problem-solving groups and supporting continuous quality improvement projects, provide examples of how you've successfully tackled quality issues in the past. Use metrics or outcomes to illustrate your impact.
Tailor Your Application: Customize your application materials to reflect the language and requirements mentioned in the job description. Use keywords related to supplier management, audits, and corrective actions to align with what the company is looking for.
Wie du dich auf ein Vorstellungsgespräch bei Whatjobs vorbereitest
✨Showcase Your Experience
Be prepared to discuss your minimum 5 years of experience in quality within the pharmaceutical or medical device industry. Highlight specific projects where you implemented quality standards like ISO 9001 & 13485.
✨Demonstrate Knowledge of Quality Tools
Familiarize yourself with quality tools such as 5P, 5M, and 8D. Be ready to provide examples of how you've used these tools in past roles to solve problems or improve processes.
✨Prepare for Technical Questions
Expect questions related to supplier management processes and audits. Brush up on your knowledge of supplier selection, evaluation, and handling complaints to demonstrate your expertise.
✨Communicate Effectively
Since good comprehension and writing skills in English are required, practice articulating your thoughts clearly. Use concise language and be ready to explain complex concepts simply.