Proactive team player, striving to find best solutions in a collegial team environment
Self-organized, self-motivated, and able to work independently
Excellent communication and presentation skills, and ability to interact with internal and external partners
Strong leadership skills and ability to manage and motivate teams to achieve goals
Ability to navigate and adapt to a dynamic and fast-paced work environment
Lead the TUB-030 Program from the PM perspective and serve as back-up to other programs
Management
Verantwortlichkeiten
Lead outsourced packaging, labelling, and distribution of CTM to support global clinical trials
Ensure timely, compliant delivery of investigational products in partnership with CMC, Clinical Operations, QA, and Regulatory Affairs
Translate study requirements into supply plans, manage inventory across depots, and maintain IRT systems
Develop budgets, forecasts, and risk assessments, providing updates to SVP CMC
Procure comparator/commercial products as needed and oversee global logistics
Ensure vendor compliance and collaborate with CMC/QC on expiry management
Anforderung
Experience managing global clinical supply, including early- and late-phase trials and working with CMOs
Strong knowledge of clinical protocols, IRT systems, and regulatory requirements
Hands-on expertise in forecasting, supply-demand planning, and inventory management
Excellent project management, organizational, and communication skills
Ability to thrive in a matrix environment, handle shifting priorities, and collaborate with cross-functional teams
Willingness to travel and work flexible hours as needed
Strong leadership, organizational, and interpersonal skills with the ability to inspire and motivate cross-functional teams
Fluent English ; German is a plus
Development
Verantwortlichkeiten
Support Process Development and GMP manufacturing of ADCs
Participate in cross-functional project teams and provide regular progress updates during the CMC team meetings
Contribute to assess GMP supply chain and help define production planning
Conduct literature research and prepare conjugation, purification, and analysis plans
Maintaining clear and current documentation, writing SOPs, Risk Assessments and reports
Processing deviations and change controls in close cooperation with Quality Assurance
Participate in or lead continuous improvement projects
Review development reports, master batch records, executed batch records and campaign summary reports. Work closely with Quality Assurance in the review process
Anforderung
Working knowledge of the requirements of GMP manufacturing
Solid understanding of requirements of at-scale manufacturing of drug-substances
Experience of manufacturing drug products is a plus
You are highly motivated and independent with excellent communication and interpersonal skills. You feel comfortable effectively working in a dynamic and multidisciplinary team atmosphere
You have either a PhD in biotechnology, chemistry or biochemistry plus a minimum of 3 years of pharmaceutical experience or Masters’ degree plus 5 years of working experience in a pharmaceutical company
Manager
Anforderung
Strong knowledge in clinical development in Oncology development is required
Self-organized, self-motivated, and able to work independently
Excellent written communication, oral communication, and presentation skills are required
Grow & thrive: Develop your career in a supportive, fast-moving environment
Significant experience with data integrity, exploration, analysis and presentation
Proactive team player, results-oriented, and striving to find best solutions in a collegial team environment
At Tubulis, curiosity and innovation drive us to transform cancer treatment. We are a fast-growing biotech where science meets passion—and where you have the chance to grow with us