Material Planner Clinical Trials (m|f|d)

at  Miltenyi Biotec

Company Description
Miltenyi Biomedicine is a biopharmaceutical company committed to advancing personalized cell and gene therapies. We are pioneering groundbreaking therapies for serious life-threatening diseases, and reshaping their accessibility for clinical professionals and patients worldwide with the aim to improve and extend patients’ lives. We are currently focusing on difficult-to-treat hematological cancers using CAR-T and other technologies, while also exploring treatments for other diseases. Our lead candidate, a tandem CAR T-cell product, is currently undergoing pivotal clinical trials on a global scale.
Join our highly professional Clinical Research & Development team in bringing new medicines to market and ensuring the safety of our pharmacological developments at all stages.
Job Description

In this multifaceted role, you will oversee the availability of materials essential for the production of investigational medicinal products, their use in our contract laboratories and for the further development of workflows that streamline standard operating procedures. You will devise comprehensive plans for existing and new processes, implement them in collaboration with the relevant departments and serve as a liaison between all departments along the supply chain.

• You ensure the availability of materials in clinical studies by forecasting and analyzing requirements.
• You assume the interface function between purchasing and production planning as well as escalation in the event of material bottlenecks.
• Another crucial responsibility is the development and implementation of comprehensive concepts for existing and new processes in collaboration with the relevant specialist departments.
• You are also involved in the further development of work processes and the creation of corresponding standard operating procedures.
• Furthermore, you actively participate in internal and cross-departmental project meetings.

QUALIFICATIONS

• You have successfully completed a degree in engineering or business administration, vocational training with a focus on logistics or supply chain management, or a comparable qualification. A degree in the natural sciences is also a solid foundation.
• Work experience in a commercial, GMP-regulated production environment, in a central laboratory or in the pharmaceutical sector is an advantage.
• You possess the organizational talent to communicate effectively, maintain reliability, pay close attention to detail, and oversee projects.
• You are highly proficient in MS Office, particularly Excel, and have experience with SAP.
• Your proficiency in German (C1) and English (B2) equips you with the confidence to thrive in an international environment.
  Additional Information

• You ensure the availability of materials in clinical studies by forecasting and analyzing requirements.
• You assume the interface function between purchasing and production planning as well as escalation in the event of material bottlenecks.
• Another crucial responsibility is the development and implementation of comprehensive concepts for existing and new processes in collaboration with the relevant specialist departments.
• You are also involved in the further development of work processes and the creation of corresponding standard operating procedures.
• Furthermore, you actively participate in internal and cross-departmental project meetings