Senior Consultant SAP Quality Management (f/m/d)

Senior Consultant SAP Quality Management (f/m/d)

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We are looking for a Senior Consultant SAP Quality Management (f/m/d) to join our Risk & Regulatory division starting from December 2025 .

Your responsibilities

• Quality Management Transformation – Actively shape digital transformation in quality management. Advise companies on selecting and implementing innovative technologies to make their quality processes future‑ready and compliant with regulatory requirements.
• SAP S/4HANA QM Expert – Dive into complex transformation projects and learn the most important trends in ERP quality management. Analyze and optimize our clients' quality processes – from initial conception through implementation, ensuring GxP compliance and regulatory adherence.
• Development – Contribute your ideas and actively drive the advancement of our consulting and audit services in Pharma quality management. Learn from experienced colleagues and grow with exciting challenges in client environments ranging from mid‑market companies to DAX corporations.
• Technologies – Engage with innovative solutions such as AI, Cloud Computing, and RPA, developing new approaches to master our clients' challenges in quality management, validation, and regulatory compliance.

Your profile

• You hold a completed degree in Life Sciences, Engineering, (Business) Computer Science, Quality Management, or a comparable field of study.
• Strong knowledge in quality management, GxP regulations, and business processes distinguishes you. You also have initial practical experience with SAP S/4HANA QM module and/or comparable quality management systems in regulated industries.
• You enjoy working in teams where you convince through analytical thinking and strong communication abilities. Your natural curiosity drives you to constantly acquire new knowledge and familiarize yourself with new systems and areas of responsibility, particularly in validation and compliance contexts.
• Understanding of pharmaceutical regulations (GxP, FDA, EMA), medical device standards (ISO 13485), and quality standards (ISO 9001) is highly valued.
• Excellent German and English skills, both written and spoken, complete your profile.

Your benefits

• Flexibility – We encourage you to choose your working hours and your working place the way that suits you and your lifestyle. We do not have core working hours and we also offer you the possibility of home office or temporary work from abroad. Always in accordance with operational requirements and labor law regulations.
• Master Program – We are passionate about your personal and professional development, therefore we offer your regular training with our internal Academy, international experiences by doing a secondment and continuous mentoring on the job. We also offer the possibility of Master's funding for examination Masters and specialization Masters.
• Lifestyle – You can accumulate overtime on your annual working time account (JAZ) and compensate for it with time off after busy periods. Any remaining overtime is paid out once a year. You also have 30 days of vacation per calendar year.
• Health and Wellbeing – Your health is important to us: in addition to our own company health insurance scheme, we also offer preventive medical check‑ups and diverse sport offerings. Take part in our free company sports programme or benefit from reduced rates at various gyms or an Urban Sports Club membership.
• And there is even more – It is our purpose to create a positive working environment: An environment where flexible and creative working is possible, where work is recognised and performance is rewarded and of which we are all very proud. You can find more detailed information on all of our benefits on our career website.

Contact

If you have any questions about this position or your application, please reach out to Nadine Beth at .

Seniority level

Mid‑Senior level

Employment type

Full‑time

Job function

Consulting

Industries

Accounting and Legal Services

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