Director QA Protein Modality

Mainz, Germany \| full time \| Job ID: 11718

About the role:

The Director of Product Quality is accountable for end\-to\-end quality oversight of small molecule and antibody program(s) throughout clinical development, commercialization, filing, approval, launch and post\-approval lifecycle management activities. This oversight includes setting and maintaining overall Quality strategies in support of commercialization efforts including: establishing relevant product quality standards for current or novel technologies, ensuring internal and cross\-functional alignment with industry and regulatory expectations, identifying product quality risks and mitigations throughout development of the assigned program(s).

This role is also responsible for setting up critical systems and standards related to Product Quality across the Global BioNTech network. The candidate will have an excellent understanding of worldwide quality regulations, especially related to drug development and commercialization.

Your Contribution:

• Provide clearly defined Quality expectations and a Quality strategy for the assigned program(s) within the BioNTech product portfolio


• Critically evaluate new products and processes with respect to Quality and compliance requirements. Work with development and product supply functions to improve manufacturing processes, new product introduction standards, and overall program strategy and keep current with global regulatory expectations


• Identify risks and proactively work with project teams and stakeholders to mitigate risks during clinical development, validation, submission, and launch.


• Creating structured approaches to communication and governance to support the product quality network


• Leading and influencing cross\-functional teams to define and effectively implement product lifecycle processes and standards


• Provide a network for product intelligence and ensuring product information is available and approved


• Provide quality support for preparation of CMC clinical and commercial regulatory submissions and associated Health authority questions for the program(s) assigned


• Provide Supplier Quality Oversight for key CDMOs

• Minimum Bachelor’s degree (or University equivalent), Life Sciences or similar technical/scientific degree


• Minimum of fifteen (15\) years industry experience or 12 years' experience with an advanced degree in Quality Assurance


• Previous experience in an FDA or EMA (and/or other Health Authority) regulated environment and familiar with Health Authority regulations and guidance


• Demonstrates expertise of compliance requirements, and an understanding of current global and regional trends in compliance


• Experience in pragmatic implementation of cGMP and regulatory guidelines


• Knowledge of compliance requirements for manufacturing and testing mRNA or biologics preferred


• International and Domestic Travel required up to 20%


• Refined colloquial and correspondence skills in English; presentation skills adaptable to all levels of internal and external stakeholders

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 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\) 6131\-9084\-1291 (Monday\-Friday from 1 PM to 3 PM CET).

Job ID 11718 (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.

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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

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