Associate Director CMC Project Management (mAB/ADC)

Mainz, Germany | full time | Job ID:9729

As Associate Director in the CMC Project Management Team at BioNTech, you will play a pivotal role in co-leading cross-functional teams alongside the CMC Lead for late-phase development projects focused on our protein/antibody-drug conjugate (ADC) pipeline. This role combines strategic project management with hands-on coordination responsibilities, ensuring seamless execution across all CMC-related activities. You will be instrumental in establishing robust project structures and driving interdisciplinary collaboration to deliver on BioNTech’s mission and goals. The position also involves close collaboration with several BioNTech Entities worldwide as well as with major pharmaceutical partners, contributing to joint development efforts and shared objectives.

• Cross-functional planning, coordination and execution of BioNTech’s protein-based CMC oncology projects, ensuring delivery of project goals (scope, budget, time, quality) in tandem with the CMC Lead
• Monitoring and controlling project progress, including budget & timeline tracking and risk management
• Driving multiple interdisciplinary teams (internal and external, including CDMOs) to ensure project scope and goals are delivered on time and with high quality
• Establishing and maintaining efficient communication structures among internal and external stakeholders, ensuring consistent information flow and alignment across teams
• Regular reporting to executive management, including preparation of project reviews and status updates
• Hands-on support of Subject Matter Experts (SMEs) in individual work packages and specific technical areas
• Building, maintaining, and managing high-performing project teams, fostering collaboration, accountability, and continuous improvement
• Leading and supporting implementation of new processes and improvement initiatives to optimize operational efficiency across the department and companywide

• A successful university degree in Chemistry, Biotechnology, Biology, Engineering, Life Sciences, or a related field
• Several (5+) years of experience in project management and coordination, ideally in regulated environments (e.g., GCP/GCLP, GMP)
• Proven CMC expertise in late-stage development projects, with a solid understanding of the drug development lifecycle
• Experience in monoclonal antibody/ADC projects and oncology is highly desirable
• Strong interpersonal skills with the ability to influence without authority, motivate teams, and build productive relationships with stakeholders
• Demonstrated leadership experience and ability to manage complex cross-functional teams
• Quick grasp of new knowledge, efficient problem-solving skills, and high personal commitment
• Ability to thrive in a fast-paced, dynamic environment
• Excellent communication, presentation, and stakeholder management skills
• Fluent English skills (written and oral); German skills are desirable but not essential

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