ich

Pauwels Consulting seeks an expert to lead regulatory dossier assessments and gap analyses for EU submissions, aligning with ICH and CMC requirements. You will identify risks, develop justifications, and shape remediation plans to support health authority responses.The role demands 8+ years in pharma or life sciences, strong technical writing and stakeholder...

Pauwels Consulting is seeking a professional to coordinate validation and planning activities within capital projects in Belgium. The role focuses on ensuring compliance with international quality standards while managing technical documentation and laboratory equipment qualification.You will collaborate with engineering and quality assurance, manage change...

Telix Pharmaceuticals is seeking a QC professional to lead and coordinate QC inspections and tests for raw materials, in-process samples and finished products in a cGMP environment in Seneffe, Belgium. Reporting to the Quality Control Manager, you will support analytical development, qualification, calibration, and deviation management while ensuring...

Normec Advipro zoekt een ervaren Freelancer in Life Sciences om sleutelprojecten te leiden en te coördineren binnen de farmaceutische en biotech sector.Je werkt aan projecten op gebieden zoals QA, Engineering, Validatie en Kwalificatie, en houdt je continu bezig met de naleving van internationale wetgeving en industriestandaarden (FDA, Eudralex, MDR, MHRA,...

RumeXperts, CRO vétérinaire indépendant, recherche un biostatisticien(ne) expérimenté(e) pour renforcer l’équipe et contribuer activement à la conception, l’analyse et à la valorisation scientifique de nos essais cliniques.Vous concevrez les plans d’analyse, réaliserez les analyses statistiques et rédigerez les rapports et publications, en...

Agencja Pośrednictwa Pracy NEXT s.c. w Belgii poszukuje Technika instalacji chłodniczych. Osoba zatrudniona na tym stanowisku będzie odpowiedzialna za montaż, utrzymanie oraz naprawy instalacji chłodniczych, zapewniając ich efektywne i bezpieczne działanie.Oferujemy bardzo atrakcyjne wynagrodzenie od 20 EUR/h brutto, dodatki do wynagrodzenia oraz...

FunctieomschrijvingJouw rol als Senior QA Cleaning Validation EngineerAls Senior QA Cleaning Validation Engineer speel je een centrale rol in de kwaliteitsborging binnen een farmaceutische productieomgeving. Je ziet erop toe dat alle vereisten rond cleaning validation en compliance correct worden toegepast en werkt daarbij nauw samen met QA, MSAT en...

Delta Healthcare Consulting zoekt in Willebroek een clinical trial assistant om als administratieve spil te fungeren voor lopende klinische studies. Je beheert administratieve taken en voorraden en fungeert als contactpunt voor de planning van deelnemers.Onze ideale kandidaat heeft minimaal 2 jaar ervaring in klinische studies, beschikt over een ICH-GCP...

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...

argenx SE is seeking a Quality Compliance Lead to drive the effectiveness and compliance of the QMS, owning deviations, change controls, continuous improvement, and quality intelligence. You will partner with Quality, Regulatory, Manufacturing, and other functions to strengthen oversight and ensure inspection readiness. The role requires 7–10 years in a...

Capgemini Engineering is seeking a Vendor Quality Specialist to support GCP vendor qualification, Quality Agreement lifecycle, and CAPA management within a regulated pharmaceutical environment. The role collaborates with Procurement, Legal and Quality Leads to ensure compliance with EMA, FDA and ICH guidelines, while driving process improvements and digital...

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...

Akkodis is seeking an experienced HVAC project engineer to lead end-to-end HVAC projects within a pharmaceutical environment in Belgium. You will coordinate equipment and piping installation, start-up and validation while ensuring safety, quality, and regulatory compliance such as GMP, ISO and ICH.The role requires a higher technical education (Industrial or...

Alimentiv independently performs, coordinates and oversees all aspects of the clinical site monitoring services, assessing protocol and regulatory compliance as per Alimentiv’s and sponsor’s standard processes, ICH/GCP guidelines and local regulation. Serves as the primary liaison between sponsor/Alimentiv and investigative sites by playing a critical...

IQVIA Belgium is seeking a Clinical Research Associate (Junior–Senior) to join our Sponsor dedicated team. You will gain experience across therapeutic areas and build a meaningful career within our organization.Based in Belgium, you will perform site visits, support recruitment planning, and ensure regulatory compliance with GCP/ICH guidelines. You will...

Job DescriptionLe spécialiste en validation et transfert de méthodes jouera un rôle crucial dans la validation, la vérification et le transfert des méthodes analytiques au sein de l'entreprise. Le candidat idéal aura une expérience significative dans la validation/vérification des méthodes analytiques dans l'industrie pharmaceutique et une solide...

AL Solutions is seeking a Senior Clinical Research Associate to lead set-up, monitoring, and oversight of Phase I–IV trials in Belgium, with occasional travel across the Benelux region. You will ensure compliance with ICH-GCP, EU regulations, and study protocols, while mentoring junior staff and coordinating with Sponsors and investigators.The role offers...

Alimentiv is seeking an experienced CRA leader to independently perform and oversee clinical site monitoring, ensuring protocol and regulatory compliance across ICH‑GCP standards. You will mentor CRA I/II and collaborate with cross‑functional teams, while coordinating audits and site initiation efforts.The role requires up to 40–60% travel, strong data...

Medpace is seeking an experienced Clinical Trial Manager to join our Belgium-based team in Leuven. You will oversee day-to-day project operations across Phases 1-4, act as primary Sponsor contact, and ensure compliance with ICH/GCP and contractual requirements.We welcome experts in Oncology/Cardiovascular/Endocrine/Metabolic who can either continue in their...

IQVIA Biotech in Belgium is seeking an experienced Clinical Research Associate to join the EU Clinical Monitoring team. You will participate in Phase I-IV trials, perform site evaluations, initiation visits, and ongoing monitoring in line with GCP/ICH.The role requires 1-2 years of on-site monitoring, strong communication skills in Dutch and English, and the...