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argenx is seeking a Regulatory CMC expert to lead global regulatory strategy for large molecule programs, from pre-clinical through commercial stages, in a rapidly expanding biotech environment.You will author and review regulatory submissions, coordinate with internal teams and external partners, and ensure timely delivery while aligning with ICH, FDA, EMA...

Alsinova is seeking an experienced Clinical Statistician to lead studies from design through execution within a CRO framework. The role emphasizes statistical strategy, protocol input, and robust analysis planning in collaboration with project teams.Ideal candidates have 3–5 years Biostatistics experience, strong SAS skills, and familiarity with...

PwC Belgium seeks an Associate Regulatory Affairs Advisor with initial pharma or life sciences experience to support regulatory strategy and submissions. You will collaborate with multidisciplinary teams across the product lifecycle, navigating EMA and FDA guidelines to help our clients stay compliant and competitive.The role emphasizes regulatory...

Alsinova, part of the Astek Group, is actively seeking Regulatory Affairs Consultants to support clients in Belgium. You will work across projects from small biotech to large pharma, handling regulatory submissions and liaising with EMA/FDA guidelines.The role involves CMC considerations, cross-functional collaboration, and delivering high-quality regulatory...

📢 We’re Hiring: Inspection Management Lead Our client is looking for an experienced Inspection Management Lead to support global pharmacovigilance (PV) activities and inspections. This is an exciting opportunity for a senior professional with strong expertise in PV inspections, inspection readiness, and GVP compliance. Your responsibilities • Drive...

Functie Als Inside Sales Employee (M/V/X) kom je terecht in het team dat zich elke dag inzet voor het uitvoeren van audits en certificatie van managementsystemen conform de ISO-, EMAS- en VCA-normen.Hiermee helpen we onze klanten hun processen te verbeteren, hun managementsystemen nog beter af te stemmen op de behoeften en verwachtingen van hun...

Would you like to join an international company on a human scale in Brussels and gain valuable professional experience? We are looking for a versatile Travel & Customer Care Assistant to support the DiscoverEU team in delivering smooth travel coordination and high-quality participant support.Travel & Customer CareRespond promptly to participant enquiries via...

Work Location: EMA Cargo West, East Midlands Airport, Derby, DE74 2TRHours: Full time - Rotating day/night roster, with weekend shifts includedSalary: CompetitiveDHL Air (UK) Ltd is the largest all-cargo air carrier in the UK, operating a fleet of B757-200, B767-300 and B777-200 aircraft on worldwide operations. Part of the DHL Express team with our...

Join us as we transform immunology and deliver medicines that help autoimmune patients get their lives back. argenx is building a new kind of biotech company, focusing on science‑based innovation.The Toxicologist in the PharmTox group will lead product risk assessments for late‑stage and established assets, shaping our approach to safety for programs...

Your next challenge Ready to make a difference? Here's what awaits you. As a Laboratory Projects Specialist, you will be at the heart of analytical projects that support the development of new medicines. Acting as the link between internal laboratory teams and project requirements, you will coordinate analytical activities, ensure high-quality deliverables...

Your next challenge Ready to contribute to the quality and safety of life-changing therapies? Here's what awaits you. As part of the growth of our Bioassays activities and the expansion of our laboratories, we are looking for several scientists to contribute to the analytical data that supports the development of innovative therapies. Depending on your...

Responsibilities Management of local (BeNeLux) regulatory activities to obtain marketing authorizations for pharmaceutical products Management and/or support of activities as Responsible for Information and Publicity (RIP) Management of local (BeNeLux) pharmacovigilance activities including input to safety reports and management of ICSR as local...

ph3WHO WE ARE /h3 pWe are Kintiga, a pan-European specialist that partners with ambitious health technology developers through the complex journey to achieve successful patient access across Europe, with our tailored approach, global perspective and local expertise. Kintiga unites three companies: MAP Patient Access (UK), AxTalis (Benelux), and SKC...

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description The Global Regulatory Lead is a key member of the global regulatory team. This role serves as a close business partner and facilitator of regulatory activities and is expected to contribute to developing sound regulatory strategies globally. The role will play a critical role...

Anacura, a family-owned, growing center of excellence in healthcare with over 300 employees consists of 4 independent business units: Labo Nuytinck, active in medical analytics and Anabiotec, OHMX.bio and Discovery Studio, active in drug development. The labs have their main activities in a state-of-art building in a green surrounding near Ghent,...

Contribute to creating a better tomorrow The only way we can tackle the challenges of this fast-changing world is with passionate people. Led by our purpose of building trust and solving important problems, we come together at PwC to address the biggest issues facing the world in a way that drives positive impact. Are you eager to join a team fuelled by open...

As a quality and compliance expert, you will be responsible for ensuring that GxP systems and processes adhere to the applicable regulatory requirements throughout the entire system lifecycle. Therefore, you stay up to date about evolving regulations from authorities such as the EMA and FDA and industry standards like GAMP and ISO. Depending on your role and...

Join our HPLC / (U)HPLC teams As we continue to grow – and with the launch of MITOSE, our new state-of-the-art facility that doubles our analytical capacities – we’re building a talent pool of chromatography specialists like you to support our future ambitions in physico-chemistry. With your expertise in liquid chromatography, you’ll directly...

You will be the analytical engine behind our clients' most challenging impurity investigations. You will design and execute highly sensitive mass spectrometry methods to ensure the safety and compliance of pharmaceutical products.Design, develop and validate sensitive and robust analytical methods for trace-level analysis quantification (with a primary focus...

WHO WE ARE We are Kintiga, a pan-European specialist that partners with ambitious health technology developers through the complex journey to achieve successful patient access across Europe, with our tailored approach, global perspective and local expertise. Kintiga unites three companies: MAP Patient Access (UK), AxTalis (Benelux), and SKC Consulting...