Director External Supply Organization (Mainz, RP, DE, 55131)
About this opportunity
Mainz, Germany | full time | Job ID: 11731
About the role:
BioNTech is a leading global biotechnology company developing innovative therapeutic approaches to combat severe diseases. Our vision is to revolutionize the way diseases are treated, providing patients worldwide with a better future. As Director External Supply Organization, you will act as the central interface between assigned CDMOs and BioNTech, ensuring smooth operations, effective communication, and strategic development of our external manufacturing network. This role is critical for driving BioNTech’s supply strategy and enhancing our protein and mRNA production capabilities.
Your Responsibilities:
Serve as the central interface between assigned CDMOs and BioNTech to ensure smooth operations and supply, as well as effective communication and collaboration
Lead interdisciplinary teams, including SMEs from AS&T, QC, MS&T, Procurement, CMC, Supply Chain, QA, Regulatory Affairs, Finance, and other areas to manage CDMO performance effectively (incl. KPI target setting, review processes, and CAPA implementation)
Lead contract negotiations and act as the first escalation point for challenges within the external production network
Execute, manage, and/or support projects at CDMOs such as continuous improvement initiatives or technology transfers
Support the supply strategy process with a focus on BioNTech's protein pipeline and mRNA pipeline; knowledge in protein and mRNA manufacturing is preferred
Drive strategic account development of CDMOs within BioNTech's external production network (incl. resource planning and budgeting)
A good match:
Completed degree in a relevant field such as supply chain management, international business management, engineering or life sciences
5–7 years of experience in the pharmaceutical or biotech industry with a focus on external supply/CDMO/supplier relationship management
Strong leadership qualities with proven project management skills and stakeholder management experience to lead interdisciplinary teams effectively
Excellent communication skills with a strong track record in contract negotiations
Strategic mindset combined with operational expertise; ability to make flexible yet thorough decisions in a dynamic environment
Profound knowledge of EMA/FDA regulatory standards as well as Good Manufacturing Practices (GMP)
Business-fluent English; German is a plus
Your Benefits:
Company Pension Scheme
Childcare
Jobticket
Company Bike
Special Vacation
... and much more.
Apply now - We look forward to receiving your application!
Apply to our Mainz, Germany location by sending us your documents via our online form. For any questions, contact our talent acquisition team on + 49 (0) 6781 9855 220.
Job ID 11731 (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.
Note for applications within Europe: Please note that if you wish to claim travel expenses incurred in connection with an in-person interview, we are obliged to carry out a sanctions list check*. This is carried out by our partner, HireRight. Travel expenses will only be reimbursed if this sanctions list check does not yield any matches. Reimbursement can be made provided that the check is successfully completed.
* Your first name, surname and date of birth will be processed for the sanctions list check. The legal basis for carrying out the sanctions list check for positions at BioNTech in Europe is BioNTech’s legitimate interest. Please note that BioNTech will not carry out the sanctions list check if no travel expenses are to be reimbursed. If you do not give BioNTech your consent to the sanctions list check, your travel expenses cannot be reimbursed. This will not affect your application.
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Job details
How this role compares
Computed from every other active Manufacturing & CMC role in our database, not just this employer's listings.
We currently track 309 comparable Director Manufacturing & CMC roles across 47 biopharma companies.
Salary context
166 of 309 peers report a salary range (USD, annualized)
Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.
Where these roles are based
Top locations among the 309 comparable roles
+ 13 more countries
Seniority mix
309 of 309 peers have a known seniority level
Therapeutic area mix
5 of 309 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden
Similar opportunities
The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.
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How we calculate "similar"
No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.
Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.
0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.