Quality Engineer (m/w/d) Complaint Handling/Post Market Surveillance - zunächst auf 24 Monate befristet

**(Senior) Quality Engineer, Post-Market Surveillance (m/f/d)**
As a
**(Senior) Quality Engineer (m/f/d) in Post-Market Surveillance** , you will be part of our Post-Market Surveillance team at our Freiburg site. Your primary responsibility will be to investigate complaints from the field, including complaints related to patient-specific products within the Craniomaxillofacial business.
**What We Offer**
Conduct structured investigations of reported field cases, including cases involving patient-specific products. You will investigate both technical and clinical aspects and collaborate with subject-matter experts from the relevant functions.
Discuss and evaluate individual cases based on the investigation results, risk assessments, and manufacturing data. In this role, you will work closely with partners from Quality, R&D, Manufacturing, Regulatory Affairs, and Clinical Affairs.
Independently analyze data, including identified failure modes and root causes, to detect critical developments and emerging trends.
Actively contribute to operational, cross-functional projects aimed at achieving sustainable product improvements. You will also serve as the key point of contact for the field performance of your assigned product portfolio.
**What You Bring**
**Required Qualifications**
A completed technical degree in mechanical engineering, medical engineering, materials science, or a comparable qualification.
Initial practical experience in a quality function or a quality-related role within a regulated industry, such as medical technology, pharmaceuticals, or automotive, is an advantage. This may include internships or working-student experience. Depending on the candidate’s level of experience, the position may be offered at a more senior level.
Strong analytical thinking and problem-solving skills, with experience in root cause analysis and trend identification.
A collaborative mindset and strong communication skills, with an interest in working across functions.
Very good written and spoken German and English skills.
**Preferred Qualifications**
Experience with ISO 13485 and Post-Market Surveillance requirements under Regulation (EU) 2017/745, also known as the EU Medical Device Regulation.
**Germany Pay Ranges:**
**Freiburg/Stetten 35Std** : €3.753 - €6.225 EUR Monthly
**Freiburg/Stetten 39Std** : €4.182 - €6.937 EUR Monthly
Bei Stryker sind wir davon überzeugt, dass Transparenz Bewerber:innen dabei hilft, fundierte Entscheidungen für ihren nächsten Karriereschritt zu treffen. Die Vergütung spielt dabei eine wichtige Rolle und deshalb möchten wir transparent aufzeigen, wie sich die Vergütung für diese Position zusammensetzt. Die Vergütungsinformationen werden je nach Position entweder als Gehaltsspanne oder als fester Betrag angegeben. Zusätzlich zum Grundgehalt können, sofern zutreffend, Bonuszahlungen und/oder Provisionen vorgesehen sein. Darüber hinaus profitieren Mitarbeitende von den umfassenden Benefits von Stryker.
Wenn Sie mehr über das Gehalt oder die Benefits dieser Position erfahren möchten, erläutert Ihnen Ihr:e Recruiter:in die Details gerne im weiteren Verlauf des Bewerbungsprozesses.
Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.
Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer – M/F/Veteran/Disability.