Director* Clinical Trial Supply Management IMP Logistics

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Become a member of the BioNTech Family!

As a part of our team of more than 2.500 pioneers, you will play a key role in developing solutions for some of the most crucial scientific challenges of our age. Within less than a year, we were able to develop our COVID-19 mRNA vaccine following the highest scientific and ethical standards – writing medical history.
 
We aim to reduce the suffering of people with life-changing therapies by harnessing the potential of the immune system to develop novel therapies against cancer and infectious diseases. While doing so, we are guided by our three company values: united, innovative, passionate. Get in touch with us if you are looking to be a part of creating hope for a healthy future in many people's lives.

Director* Clinical Trial Supply Management IMP Logistics

At BioNTech, you will set up complex structures to ensure efficient and timely end-to-end supply of our clinical trials with investigational medicinal products in an innovative international environment in compliance with regulatory requirements. Your main responsibilities are:
  • Lead and develop the CTSM Logistics team within Clinical Trial Supply Management Department to support the achievement of company goals of the R&D program portfolio including risk-based decision-making and prioritization
  • Responsible for identifying gaps and driving improvements in CTSM logistics processes with increasing complexity and documentation across all associated functions, all applicable BioNTech entities and across all clinical programs. This includes responsibility for critical decision making processes in coordination with internal and external stakeholders
  • Take leading role in audits and inspections of Clinical trial Supply Management and the management of respective findings and communication of changes to the respective internal and external stakeholders
  • Responsible to integrate continuously new regulatory guidelines and regulations into organization´s clinical trial supply and logistics processes and standards to ensure state-of the-art operations and compliance to legal requirements in close collaboration with internal and external functions
  • Ensure that Quality-related processes are kept

What you have to offer.

  • Degree in supply chain management, pharmacy, chemistry, biotechnology, or related discipline or engineer with profound understanding of clinical supply logistics
  •  Many years of experience in Clinical Trial Supply Logistics Management in pharmaceutical or biotech industry setting
  • Very sound knowledge and documented experience in relevant legislation and international GDP guidelines and also in customs regulations and impact of supply chain activities on product quality
  • Demonstrated quality management experience and proven track record of warehousing and distribution of study drugs
  • Profound knowledge and experience in cold chain logistics including impact of product properties and stability on supply chain activities
  • Proven track record of effective capture and integration of latest clinical supply logistics trends and profound understanding of electronic systems supporting logistics processes
  • Business-professional English language skills

Benefits for you.

  • Company Pension Scheme
  • Childcare
  • Jobticket
  • Company Bike
  • Leave Account
  • Fitness Courses
  • Mobile Office
  • Special Vacation
... and much more.

Have we kindled your pioneering spirit?

Then apply now for our location Cambridge, Massachusetts, Mainz and simply send us your application documents using our online form.

If you have any further questions, our Talent Acquisition Team will be happy to answer them on + 49 (0) 6131-9084-1291 (monday-friday, from 12 noon to 4 pm).

Job-ID 6653 (please indicate for inquiries)

We look forward to your application!

*BioNTech does not differentiate on the basis of gender, race or ethnicity, religion, color, sexual orientation or identity, disability, age and other protected statuses as given by applicable law. We are committed to creating a diverse environment and are proud to be an equal opportunity employer. Most important – it’s a match!

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