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Director CTSM, Supply & Data Integration

BioNTech AG -
Mainz

Jetzt bewerben

Details zur Stelle

Vollzeit
vor 10 Tagen

Leistungen

Jobticket
Flexible Arbeitszeiten
Kostenfreies oder vergünstigtes Deutschland-Ticket

Qualifikationen

Doktorat
Informationssysteme
Führungserfahrung

Vollständige Stellenbeschreibung

London, United Kingdom; Mainz, Germany; Munich, Germany | full time | Job ID: 11624

About the Role:

As Director CTSM Supply & Data Integration, you will lead the deployment, configuration, and optimization of BioNTech’s Intelligent Clinical Supply Management (ICSM) SAP module within our global Clinical Trial Supply Management (CTSM) division. Acting as a strategic counterpart to IT, you will ensure seamless data flow, accuracy of information, and optimized processes across clinical trials and external partners.
In this pivotal leadership role, you will collaborate with cross-functional stakeholders to drive innovation in clinical supply chain management. Your expertise will directly contribute to advancing BioNTech’s mission of delivering transformative therapies while setting new standards in clinical trial supply management.

Your Contribution:

Act as Business Process Owner for the CTSM digital ecosystem, including ICSM integration with systems such as S/4HANA, IRT, and vendor platforms; oversee rollout, change management, and training initiatives
Serve as CTSM Global Template Process Owner for SAP value streams (e.g., I2R, S2S, MDM), ensuring alignment with business needs through collaboration with template process owners and system stakeholders
Lead the identification and alignment of ICSM/SAP workflow requirements while managing expectations for harmonized execution of business requirements and system capabilities
Represent CTSM as Business Owner for SAP/ICSM system URS validation processes
Direct projects related to CTSM master data and integration; resolve issues, implement data governance practices, optimize processes during transformations, and enhance data reliability

A good Match:

Completed university degree in Engineering, Clinical Supply Chain Management, Quality Management, Computer Science, Information Systems, or a related field (Doctorate preferred)
Minimum 5 years of experience in Clinical Trial Supply Management within pharmaceutical/biotech or regulated industries; experience with system providers is an advantage
Proven track record in ERP/IT implementation projects such as SAP S/4HANA; expertise in ICSM modules and third-party data integration concepts
Demonstrated skills as a super user overseeing SAP-supported clinical supply processes like material management, demand/supply planning, and logistics using tools such as Kinaxis, ICSM, IRT or Veeva
Advanced experience integrating diverse data flows while managing administrative functions for data flow control and access across systems supporting clinical trial supply activities
Exceptional project management skills paired with strategic thinking and negotiation abilities; adept at making decisions that prioritize team success
Fluency in English (business-professional level); German proficiency is highly desirable
Strong leadership abilities to guide individuals with diverse professional backgrounds toward shared goals

Your Benefits:

It's our priority to support you:

Your flexibility: flexible hours | vacation account
Your growth: Digital Learning | Performance & talent development | leadership development | Apprenticeships | LinkedIn Learning
Your value: Your voice at the table | Culture on an equal footing | Opportunities to shape & impact | Support for your full potential
Your health and lifestyle: Company bike
Your mobility: Job ticket | Deutschlandticket
Your life phases: Employer-funded pension | Childcare

Apply now - We look forward to your application!

Apply to our London, United Kingdom; Mainz, Germany; Munich, Germany location by sending us your documents via our online form. For any questions, contact our talent acquisition team on: + 49 (0) 6131-9084-1291 (Monday-Friday from 1 PM to 3 PM CET).

Job ID 11624 (please always specify if you have any questions)

By submitting your application, you acknowledge that a background check will be conducted as part of the recruitment process in accordance with applicable laws and regulations. If you are considered for the position, BioNTech will conduct the background check through our service provider ‘HireRight’. You will be informed accordingly by your BioNTech-Recruiter.

Inspired? Become part of #TeamBioNTech.

BioNTech, the story

At BioNTech, we are more than just a biotechnology company – we are a community of innovators, scientists, and leaders dedicated to revolutionizing medicine by translating cutting-edge science into survival. Your contributions here have the potential to improve the health of people worldwide, especially by addressing diseases with high medical needs like cancer and various infectious diseases.

Experience a dynamic workplace that embraces diversity in all its forms. We foster innovation, encourage creativity, and develop business strategies driven by our shared passion for advancing medicine.

Working at BioNTech means striving to achieve medical breakthroughs while growing your career in a meaningful way. Apply today and become part of a mission that has the potential to change lives around the world.

BioNTech does not tolerate discrimination, favoritism or harassment based on gender, political views, religion or belief, nationality, ethnic or social origin, age, sexual orientation, marital status, disability, physical appearance, health status or any other physical or personal characteristics. BioNTech is committed to creating a diverse and inclusive work environment. We are proud to be an equal opportunity employer. The main thing is that you suit us, and we suit you!

BioNTech - As unique as you

www.biontech.com

Jetzt bewerben

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