Associate Director/Director, CMC Antibody-Drug-Conjugates (ADCs)
Associate Director/Director, CMC Antibody-Drug-Conjugates (ADCs)
Your role
- Managing (parts of) external CMC-related early and late stage development and manufacturing activities of Merus’ product candidates;
- Monitoring and updating project plans and timelines in relation to the outcome of process development work; managing critical path activities to prevent program delays;
- Ensuring that process development and manufacturing activities are conducted in line with good scientific principles and design, in compliance with regulatory guidelines and according to GMP, GLP and/or GDP, where applicable;
- Preparing/reviewing technical documents including development/manufacturing/validation/ transfer plans, reports and other critical documents of (outsourced) CMC activities;
- Leading/participating in cross-functional subteam(s);
- Selection and performance monitoring support of Contractors for CMC activities;
- Preparation and reviewing support for regulatory submissions;
- Evaluating change controls and deviations related to CMC activities;
- Reporting on status and planning of CMC activities on a pro-active basis;
- Ensure that conflicts between Merus and Contractors are timely detected and properly escalated where needed.
Your profile
- You hold at least a Master’s degree in a relevant biomedical field, and have at least 5 years of experience in CMC of ADCs in the biotech or pharma industry;
- Experience in antibody/ADC development as well as antibody/ADC drug substances and/or drug product manufacturing;
- You have good understanding of various quality systems such as GMP, GLP and GDP;
- You are a team player focused on results and on the quality of your work;
- You are known for your organizational skills, accuracy and drive to continuously improve your work;
- You communicate well in English, both verbal and in writing.
Our offer
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