Location Munich, Bavaria, Germany
Job ID R-227454
Date posted 12/06/2025
Are you enthusiastic about quality and regulatory topics in the healthcare industry? Would you like to learn and apply artificial intelligence quality practices into software research and development? Then AstraZeneca might be the one for you! In this position, you will be working within a multi-disciplinary team to support the delivery of precision medicine solutions for our Oncology portfolio. This role is based at our Munich, Germany office.

SITE DESCRIPTION - MUNICH, GERMANY.

Welcome to Computational Pathology Munich, one of over 400 sites here at AstraZeneca, providing a collaborative environment where everyone feels comfortable and able to be themselves is at the core of AstraZeneca’s priorities, it’s important to us that you bring your full self to work every day. To help you maintain your best self, here’s a sneak peek into some of the things this site provides for you: After-work events, lunch & learns, spacious environment, sustainable office working environment, events, family and childcare support and of course the Alps around the corner for hiking, biking and skiing.

WHAT YOU’LL DO

• Support the implementation of a QM system that complies with EN ISO 13485:2016 for medical device software.
• Define and improve processes by creating/updating SOPs, forms and templates to ensure conformity with applicable internal and external requirements.
• Deliver trainings on SOPs and applicable standards.
• Quality Assurance of software development process to ensure compliance with IEC 62304, international AI standards and internal processes.
• Write and contribute to product technical documentation.
• Support preparation of internal and external quality audits.

ESSENTIAL FOR THE ROLE

• Degree in engineering, natural sciences, computer science or related discipline, or 5 years of equivalent working experience.
• At least 10 years of relevant work experience in pharma or medical device industry with focus on quality and regulatory topics, and 2 years in SaMD design and development.
• Good knowledge of relevant norms and regulations for SaMD (ISO 13485, IEC 62304, ISO 14971).
• Excellent written and verbal communication skills in English and an eye for detail.
• Ability to drive, influence, manage, execute, and deliver results for complex multi-functional, interdisciplinary projects.

DESIRABLE FOR THE ROLE

• Experience with In-vitro Diagnostics medical devices (IVD) and understanding of IVD performance evaluation.
• Understanding of drug development process and companion diagnostics.