Our client is a professional Biotechnology organisation, based in Zuid-Holland Netherlands. Our client is a subsidiary of a global pharmaceutical company.
In this role you will be responsible for all subteams regarding up to 3 projects in the drug development department.The department consists of 6 teams that develop the bulk of clinical and commercial manufacturing of drug substances.
You will lead project teams and make sure that project are timely delivered. You represent the department in the CMC team and contribute to development strategies in alignment with timelines of the DSD team, clinical supply chain, regulatory and quality assurance teams.
Also responsible for risk assessment, budget preparations and keeping track of regulatory submissions done by appropriate experts.