Sapreme Technologies is a privately-owned biotech company developing a disruptive technology platform (ENDOSCAPE®) enabling the development of superior targeted therapeutics, such as antibody-drug conjugates and oligonucleotide-based drugs. We are currently expanding and have several vacancies to fill. We welcome you to take a look, share with your network, or apply directly.
Applications closed | Project Manager (part time)
In the role of Project Manager, you will assist the Sapreme team in delivering various complex projects and programs by organizing and coordinating the project and program activities. The Project Manager is responsible for setting up project management systems and implementation plans as formulated by the content stakeholders and in line with the company goals. You will be creating and maintaining project overviews per time period, per project. You will contribute to keeping projects on track, help to define and monitor deliverables and milestones. You will contribute to defining and tracking project budgets, as well as generate resource projections and resource actuals per project. Your role also encompasses the processing and visualization of project plans (such as timelines, Gantt charts, tabular overviews) to aid internal and external communication on project status updates and planning. Your project status input will support preparation of budget and content proposals. You will also help to coordinate and administer meetings and events, such as reservations, invitations, agenda preparation, document project updates, and minute keeping as required. To accomplish these objectives, you will closely work with Sapreme’s scientists and leadership and follow-up with relevant stakeholders. In your role, you will directly report to the Chief Development Officer.
Read the full job description here for more details and information on how to apply.
Applications closed | (Senior) Scientist – Pharmacology/In Vivo Biology You will be responsible for a variety of different preclinical development activities including the translation of early discovery efforts into in vivo proof of concept studies according to industry-standard quality systems. You will contribute to the design of PK/PD studies, you will supervise such studies at specialist CROs, and you are responsible for data interpretation and reporting. The role also encompasses the bioanalysis of study samples, either by setting up and performing select analyses in house or outsourcing to specialty labs. Read the full job description here. We welcome any questions you might have, please feel free to reach out to the hiring manager Miriam Bujny, or submit your application directly to: email@example.com
Applications closed | Scientific writer (part time or full time) As Scientific Writer you will be responsible for providing scientific writing and communication for different research and preclinical activities. You will support the research and development teams by writing research and preclinical study reports, patent examples describing methods and experimental results, and scientific publications (manuscripts, abstracts, presentations, posters, etc.). You will build and manage the internal and external review process of documents and oversee version control and the archiving processes. Next to this, you will maintain an inventory of relevant literature and competitor overviews. You will also be responsible for proofing scientific documents for accurate content before submission to publishers or agencies. To accomplish these objectives, you will closely work with Sapreme’s scientists and leadership and follow-up with relevant stakeholders. Read the full job description here. We welcome any questions you might have, please feel free to reach out to the hiring manager Miriam Bujny, or submit your application directly to: firstname.lastname@example.org
Applications closed | (Senior) Bioconjugation Scientist/Chemist – Conjugate Production and Characterization You will be responsible for producing a variety of customized antibody-drug conjugates, including antibody-protein and antibody-oligonucleotide conjugates. You will optimize the conjugation and purification procedures for a variety of biologics and linkers, according to industry-standard quality processes and systems. You will perform bioanalytical analyses on the resulting conjugates. You will also closely collaborate with the biological validation department to assess the activity of the conjugates. You will accurately report your work and contribute to internal project meetings. Read the full job description here. We welcome any questions you might have, please feel free to reach out to the hiring manager Ruben Postel, or submit your application directly to: email@example.com