775 English-speaking jobs in Antwerp Province

Dynamics 365 Finance Consultant will deliver a greenfield implementation of Dynamics 365 for Finance & Supply Chain Management. The role involves working closely with stakeholders, shaping, configuring, and testing business processes. Experience with General Ledger, Accounts Receivable, Accounts Payable, Cash and Bank Management, and Fixed Assets is required.

The Executive Director, Clinical Leader – Neuropsychiatry is responsible for the development and execution of clinical development plans for late-phase compounds. This role leads a cross-functional team to develop products in a timely and cost-effective manner, overseeing clinical study design, protocol development, and execution. The Executive Director will manage direct reports and collaborate with various departments, including regulatory affairs, finance, and clinical operations.

Senior Product Manager to lead a new category of active hearables. Define product vision, build business cases, and drive execution across hardware, firmware, and app development. 8+ years of product management experience in consumer tech required.

Leads late-phase clinical development (P2b/3) of neuropsychiatry compounds. Develops and executes clinical development plans, designs trials, and prepares regulatory filings. Manages a matrix-based clinical team and oversees safety and medical activities. Requires an MD with post-doctoral training and 7+ years of clinical research experience, including 3+ years in phase II/III development.

MSAT Synthetics Drug Product External Site Principal Scientist provides technical oversight to external manufacturing sites. Handles technology transfer, product life cycle activities, and material qualification. Acts as technical coordinator for CMO process technology proficiency and implementation of MSAT Technology Roadmaps. Supports site lifecycle processes and technical assessment of change controls. Requires a bachelor's degree and 8+ years of relevant experience.

Lead statistical strategy and execution for projects including solubility modeling, stability estimation, and reaction trend analysis. Develop design of experiments and Bayesian Optimization workflows.

Data Scientist to support biopharmaceutical manufacturing process optimization and innovation. Provides statistical and data science expertise across cell culture, purification, and analytical activities. Requires experience in cGMP environments and biologics manufacturing.

Leads end-to-end execution of collaboration projects from concept to market launch. Identifies and recommends collaboration opportunities. Partners with cross-functional teams to develop product briefs, manage project timelines, and ensure successful launch. Leads culture-driven product initiatives and translates cultural insights into product opportunities.

Senior Software Engineer to design, build, and evolve technology platforms for power trading operations. Responsibilities include leading development of backend services, APIs, and desktop applications, driving technical architecture, and mentoring fellow developers. Requires significant experience with .NET C#, cloud technologies, and modern software engineering practices.

Lead the direction of AI across products and organization. Shape AI features, mature data foundations, experiment with AI applications, and make strategic AI decisions.

Lead the direction of AI across products and organization. Shape AI features, mature data foundations, experiment with AI applications, and make strategic AI decisions.

Expert Consultant to support a pharmaceutical company's strategic project. Focus on documentation activities for automated systems and manufacturing equipment, including IQ, OQ, and PQ protocols. Requires DeltaV or VSI expertise, GMP/GxP knowledge, and strong documentation skills.

Agfa offers a 6-12 month internship in Applications Research for Master's students in chemical, mechanical, software, or commercial engineering.

Expert Consultant to support a pharmaceutical company's strategic project. Focus on documentation activities for automated systems and manufacturing equipment, including IQ, OQ, and PQ protocols. Requires DeltaV or VSI expertise, GMP/GxP knowledge, and strong documentation skills.

Experienced VAT Manager needed for global VAT setup in SAP (ECC and S/4HANA). Lead VAT design, configuration, and compliance processes, ensuring accurate determination, coding, and reporting. Translate complex VAT requirements into functional specifications and drive SAP VAT configurations. Collaborate with Finance, IT, Supply Chain, and Business units to embed VAT in end-to-end processes.

Leads end-to-end execution of collaboration projects from concept to market launch. Identifies and recommends collaboration opportunities that drive business growth and brand relevance. Partners with cross-functional teams to develop product briefs, manage project timelines, and ensure seamless execution. Leads culture-driven product initiatives and translates cultural insights into product opportunities.

Associate Director will accelerate complex clinical development programs through integrated planning, risk management, and cross-functional collaboration. Responsibilities include creating study schedules, identifying acceleration opportunities, and managing budgets, timelines, and resources. Requires a Bachelor's degree, 8+ years of experience in clinical development, and expertise in project management methodologies and tools.

Senior Business/Functional Analyst to support automation of social security processes for self-employed individuals. Analyzes business requirements, translates them into functional specifications, and collaborates with development teams. Requires 5+ years experience as a business/functional analyst, 3+ years in Agile/Scrum environments, and proficiency in BPMN, UML, SQL, Sparx Enterprise Architect, XML, web services, and End-to-End testing.

Leads inspection management and readiness activities for a global Pharmacovigilance organization. Supports regulatory inspections and collaborates with cross-functional teams to ensure compliance with GVP, GCP, and GLP. Requires 5-8 years of experience in Pharmacovigilance, GVP Quality, Quality Assurance, or Auditing with proven experience in inspection management.

Leads inspection management and readiness activities for a global Pharmacovigilance organization. Supports regulatory inspections and collaborates with cross-functional teams to ensure compliance with GVP, GCP, and GLP. Requires 5-8 years of experience in Pharmacovigilance, GVP Quality, Quality Assurance, or Auditing with proven experience in inspection management.