Beschreibung
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