680 English-speaking jobs in Antwerp Province

Manager, EU Medical Device & IVD Regulation, serves as SME for EU regulations, integrating them into the Clinical QMS. This role leads impact assessments and partners across global functions to support clinical research programs.

Trainee Industrial Pharmacist role applying theoretical knowledge in pharmaceutical manufacturing, testing, and release. Support continuous improvement projects across product lifecycle stages. Requires a Master after Master in Industrial Pharmacy.

Principal Engineer in R&D Process Engineering manages clinical manufacturing for synthetic-molecule drug products across oral solids, liquids, and parenteral applications. This role involves pilot plant operations and CMO network oversight.

Quality Assurance Associate to join the Clinical Supply Quality Post-Certification team. This role ensures quality and compliance of investigational medicines by investigating complaints and logistics issues across global teams.

Lead and support the implementation of innovative statistical approaches across the development portfolio. This Senior Principal Scientist, Biostatistics role involves developing methods, running simulations, and collaborating with partners.

Manager, Capacity Management shapes resource and capacity strategies across divisions, providing forward-looking insights for portfolio and investment decisions. This role owns end-to-end resource forecasting models and translates complex analyses for senior leadership.

Senior Scientist in Discovery Process Research develops novel synthetic chemistry solutions to accelerate therapeutic discovery. This role requires a PhD in Synthetic, Organic, or Medicinal Chemistry and involves solving chemistry problems across discovery projects.

Senior Scientist, Product Lead CMC Regulatory Affairs drives scientific strategy and develops global CMC regulatory strategies. This hybrid role supports global regulatory filings and prepares dossiers for Health Authorities.

Technology Deployment Leader for the IM Transcend program. This role modernizes transactional processes by harmonizing the ERP ecosystem, standardizing core business processes, and enabling an integrated data strategy using SAP S/4 HANA. Requires 15+ years of experience.

Senior Manager / Associate Director, Clinical Data Transparency, EHDS Data Cataloguing leads the operational and technical aspects of identifying, classifying, and maintaining J&J's in-scope health data under the European Health Data Space.

QC Analyst, CAR-T is responsible for quality control testing for drug product release, stability, and lentiviral batch identification, ensuring GMP compliance. The role involves analytical testing, SOP maintenance, and supporting laboratory investigations.

Lead research to develop therapeutic agents as Principal Scientist in Chemical Process R&D. Requires Ph.D. with 5+ years in process chemistry or Master's with 7+ years. Focus on experimental design and process development.

Lead a global team as Director, Regulatory Data Office Leader, overseeing the Regulatory Data Hub. Ensure trusted, high-quality regulatory data enables business intelligence and drives transformation across R&D.

Senior Scientist role focusing on LNP and t-LNP formulation and process development for parenteral and liquid drug products. Responsibilities include leading development from early stages through commercialization.

Postdoctoral Scientist - AI/ML to advance AI/ML and generative AI for drug discovery. Develop foundation models and representation learning for biological sequences, integrating AI design with lab validation. Requires strong AI/ML expertise and publication record.

Sr. Manager - IM CSV Quality Lead assesses and improves the IM strategy for computer system validation and embedded AI supporting GxP activities. This role ensures system validation and compliance with global regulatory requirements.

Manager, Process & Personnel Qualification Management drives compliance and quality excellence in the pharmaceutical industry. This role leads process improvement projects and supports digital transformation toward data-centric systems.

Senior Manager, IM R&D Procurement Category, Analytical Development & Testing. Develop and execute global procurement strategies for external analytical development and laboratory testing services. Partner with scientific and technical leaders to build supplier strategies.

MSAT Synthetics DP External Site Principal Scientist provides technical oversight to external manufacturing sites. Responsibilities include NPI, tech transfers, and lifecycle management, requiring 8+ years of relevant experience.

Associate Director, PSTS Integration & Transition Management leads preclinical and translational science integration for business development outcomes. This role coordinates diligence findings into integration plans, managing risks and dependencies across functions.