Baden-Württemberg, Freiburg Bötzinger Str 41, Germany
1 day ago
Senior Quality Engineer NPI (m/f/d)
Work Flexibility: Hybrid or Onsite

As a Senior Quality Engineer (m/f/d) New Product Introduction, you’ll help bring innovative medical technologies to market by driving quality across the full product lifecycle. Based in Freiburg, you’ll collaborate with global teams in Germany, India, Ireland (Cork), Poland (Skawina), and US to ensure new products — from line extensions to novel Trauma & Extremities solutions — meet the highest standards of safety and compliance.

What will you do:

Lead quality activities in New Product Introduction (NPI), with a focus on both line extensions and new-to-market devices

Support full product lifecycle from concept to commercial launch, including risk management, validation, and inspection planning

Represent Quality during design reviews, ensuring compliance with FDA, ISO 13485, and internal Stryker processes

Collaborate with cross-functional teams across regions to standardize NPI processes and deliverables

Support supplier qualification and PPAP activities, and support validation of external manufacturing processes

Ensure robustness of quality deliverables, including DHF, PFMEA, and CAPA input as needed

Utilize statistical tools to develop efficient, scalable inspection and production quality systems

Communicate clearly with internal teams, suppliers, and stakeholders to ensure timely and high-quality project outcomes

What will you need:

Required:

Bachelor’s degree in Engineering, Life Sciences, or related technical field

2+ years in Quality or Manufacturing within Medical Devices or Pharma (or other highly regulated industry). The seniority of the role may be adjusted based on your experience and qualifications

Strong knowledge of risk management, PFMEA, and statistics

Fluent in German and English

Strong communication, initiative, and time management skills

Comfortable working both independently and in a team environment

Preferred:

Experience with supplier quality, PPAP, validation, and supplier audits

Familiarity with FDA, ISO 13485, and NC/CAPA processes

Exposure to design control and DHF documentation

Experience in cross-functional collaboration across global teams

Diversity is important to us. We welcome applications from people regardless of their ethnic, national or social origin, gender, disability, age or sexual identity. 

 

Additional information

The position is initially limited to 12 months. Due to the large number of different positions and areas of responsibility, Stryker often offers the options of being taken on in a permanent position.

Travel Percentage: 20%

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