Qualified Person for Pharmacovigilance Permanent, Hybrid Location: Netherlands Driven by their mission to transform the lives of patients with rare, life-threatening diseases, this biopharma develop and commercialise innovative protein replacement therapies and precision medicines. Reporting to the VP of Global Pharmacovigilance, as QPPV, you will play a critical role in ensuring patient safety...
Read moreScienta are partnered with a Global player in the Life Sciences field. This global life sciences company specializes in providing technologies and services that support the development and manufacturing of biopharmaceuticals. Their offerings include products for cell culture, chromatography, filtration, and analytics, all designed to advance research and production in the biotechnology and phar...
Read moreLocation: Utrecht, Netherlands Role Overview: In this role as a key member of the Netherlands data science team, you’ll work closely with laboratory staff and international experts, influencing experimental design and delivering valuable insights. Key Responsibilities: Develop and implement advanced multimodal data algorithms to address challenges in oncology assay development. Support ex...
Read moreLocation: Netherlands (preferable), Denmark, UK or Austria. This role is only open to candidates that already have the right to work in the EU. No sponsorship available. The Company We are partnered with a rapidly growing, emerging clinical stage Biotech headquartered in the Netherlands. They are poised to make a significant impact within the field […]
Read moreStrategic Account Manager We are working with a large innovative Diagnostics/Biotech company which specialises in the field of In vitro diagnostics and offers a broad range of innovative instrument systems and tests for hospitals, reference labs, blood banks and clinics. The Strategic Account Manager role is responsible for selling solutions to hospitals/laboratory accounts/ strategic prospect...
Read moreAbout The Company We have teamed up with a truly exciting, innovative start-up that stands as a burgeoning and inventive player within the field of medical technology. The company’s central mission revolves around ensuring convenient and successful vascular access, an objective they steadfastly pursue at all times and across all settings. The team brings together […]
Read moreMy client is a global biopharmaceutical company dedicated to transforming the lives of patients with rare, debilitating, and life-threatening diseases. As a Regulatory CMC Manager/Senior Manager you will have the following responsibilities: Assisting in the development of global CMC regulatory strategies for products. Acts as CMC regulatory affairs representative on cross-functional teams to pr...
Read moreAbout the company We are working with a medium-sized Medical Device company who are digitizing the interface between the surgeon and patient to pioneer a new era of Performance-Guided Surgery. They are a well-established player in the field and they are continuing to grow quickly and further establish their presence across Europe. The client is […]
Read moreCompany Regulatory Consultancy About Scienta are proud to be working with a distinguished regulatory consultancy in Breda (Netherlands) with a focus on product development in Europe and the US. Role The role requires at least 10-15 years of drug development experience with 5 years in Regulatory Affairs for Biotech. The role is a mix of […]
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