About – This position will be involved in the expansion of in vitro binding assay capabilities to screen, characterise and evaluate the companies drug candidates. Duties Use ELISA and SPR to characterise new drug candidates. Follow established assay protocols. Maintain accurate and detailed records of samples, experiments and results. Work with international scientists to review, […]
Read moreThis position is open to applicants at Director or Senior Director level. Location: Paris, France (on-site once a week) The Company A clinical-stage biotechnology company driven by innovative R&D and first-in-class therapies is looking for a Director / Senior Director Business Development with experience in out-licensing, co-development partnerships, market analysis and competitive intellig...
Read moreMy client is a listed clinical phase biotechnology looking for a strong & established Head of Regulatory to join their growing organisation. As a Head of Regulatory you will have the following responsibilities: Provide leadership and hands on management of Regulatory Affairs their clinical and preclinical development portfolio, including CMC. You will work as the […]
Read moreAssociate Director HEOR – EU & RoW About the Company Developing products for rare diseases and unmet medical needs, this company is driven by patient-centricity. They have seen 40% growth over the last year, with two approved products already commercialised and multiple more in the pipeline. They prioritise the growth and development of their team […]
Read moreCompany – This clinical-stage biopharmaceutical company is developing the first in-class, investigational, dual-action (immune-modulating) cancer vaccine. This company’s aim is to become the essential backbone for cancer combination therapy. Location – Copenhagen, Denmark About the company This company is developing a dual-action investigational immune-modulating cancer vaccin...
Read moreAssociate Director – Safety Operations (12 month contract) Location – Zurich Switzerland Company – A small-medium sized bio-pharmaceutical company focused within unmet medical needs in the rare disease space is looking to expand. They have grown 20% in the last year alone, across both the US and in Europe! They have one product with both […]
Read morePosition Responsibilities Participate on project development teams and represent regulatory affairs by supporting project and product teams. Prepare regulatory submissions as required for global approvals for in vitro diagnostic (IVD) products, including preparation of reports and interaction with regulatory officials as required. Prepare and submit to notified body Technical Documentation need...
Read moreHead of Regulatory Affairs Want to join a growing biotech? This is a great opportunity for a Senior Regulatory expert to lead regulatory at Clinical Stage Immunology focused company. This client is seeking a hands-on head of Regulatory Affairs who will bring broad experience in regulatory affairs and operations along with a roll up the […]
Read moreCompany – A global commercial stage biotechnology company, focusing on Oncology cell therapy, developing and manufacturing novel therapies. Location – Belgium (Ghent) About the company This company develops and manufactures novel therapies with a current focus on haematology, solid tumors and infectious diseases. Due to their ongoing success, this company is now looking for a [&hell...
Read moreCompany – A global commercial stage biotechnology company, focusing on Oncology cell therapy, developing and manufacturing novel therapies. Location – Belgium (Ghent) About the company This company develops and manufactures novel therapies with a current focus on haematology, solid tumors and infectious diseases. Due to their ongoing success, this company is now looking for a [&hell...
Read moreSenior / Principal Scientist Toxicology About – This position requires extensive expertise in toxicology to help the Translational Research Team with their goal to create novel non-viral gene therapies. Duties Provide strategic and scientific leadership to the translational research team to guide the toxicology strategy for the drug candidates in the pipeline. Responsible for the […]
Read moreAbout – Here at Scienta we are teaming up with a global biotechnology company dedicated to treating, and one day curing, life-threatening diseases. They are developing advanced cell therapies across a diverse array of technology platforms – with a main focus on Oncology + Immunology. The QC Analyst, is an exempt level position with responsibilities […]
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