Associate Director* E2E Supply Chain Individualized Products

Join our team of pioneers!

As a part of our team of more than 5.000 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.

Your main responsibilities are:

Develop and maintain the E2E Product Supply Strategy and a resilient production network of sites and CMOs and manage demand, supply and utilization (including inventory, logistics and business continuity)
Execute governance and overall S&OP to assure demand is accurate and to be build in supply plans and strategies, Develop and maintain the E2E Product Supply Strategy for your assigned product/product family
Lead a matrix team across the Supply Chain organization and serves as the primary point of contact for your assigned product/product family for Supply Chain to other areas of the business (clinical & commercial per product phase)
Monitor strategic scenarios to proactively identify risks and opportunities; endorse product scenario analysis from the planning teams and allign with cross-functional interfaces
Lead continuous improvement projects to drive expanded capabilities, improve the efficiency of existing processes and enable cost reduction

What you have to offer:

Successfully completed university degree in business administration, industrial engineering or applied science
More than 7y working experience in production planning, preferably in the (personalized) pharmaceutical industry (deep knowledge of available QC capacities/regulatory timelines and clinical study demands)
Experience in handling complex strategic projects
Excellent analytical, communication and problem-solving skills as well as hands-on mentality with broad range of working scope
Ability to work in dynamic working environment with dynamic targets and expanding processes
Fluent German & English skills (written and spoken) as well as affinity for IT, including profound Excel skills and preferably SAP experience

Benefits for you:

Flexible Working Time
Mobile Office
Work from EU Countries (up to 20 days per year)
Company Pension Scheme
Childcare
Jobticket
Company Bike
Leave Account
Fitness Courses

... and much more.

Have we kindled your pioneering spirit?

Then apply now for our location Mainz and simply send us your application documents using the "Apply Now" Button.

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 7651 (please indicate for inquiries)

We look forward to your application!

*BioNTech does not tolerate discrimination, favoritism, or harassment based on gender, political opinion, religion or belief, nationality, ethnic or social origin, age, romantic orientation, marital status, disability, physical appearance, health status or any other aspect of personal status. We are committed to creating a diverse and inclusive environment and are proud to be an equal opportunity employer. Most important - it’s a match!

BioNTech - As unique as you

www.biontech.com

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Full-Time , Permanent

Specialist

Updated at 08/29/2024

While applying for the job please refer to jobvector and use the following reference number: 7651