609 English-speaking jobs in Antwerp Province

Senior ML Engineer to operationalize and scale AI/ML solutions for Biologics Discovery. Own deployment, lifecycle management, and governance of ML and generative AI models for scientific workflows. Requires 4+ years scaling AI/ML in production.

Specialist, PDM Program Expert joins QM&D to shape quality processes and learning solutions across global R&D. This role integrates regulatory and business requirements into compliant processes and training.

QC Micro Analyst supports CAR-T therapy production by performing and reviewing microbiological testing in a cGMP lab. This weekend role requires a scientific degree and 2+ years in a regulated QC environment.

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.

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.

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 scientific experimentation and process development.

Trainee Industrial Pharmacist role involves applying knowledge in pharmaceutical manufacturing, testing, and release. You will support continuous improvement projects across product lifecycle stages. Requires a Master's in Industrial Pharmacy.

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.

Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj. com . As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world.

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.

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.

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.

Sr Analyst, External Clinical Supply Quality manages quality and compliance for external suppliers handling Investigational Medicinal product packaging, labeling, and distribution. Responsibilities include supplier qualification, quality agreement review, and cGMP support.

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.

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

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

QC Analyst, CAR-T Biotech performs quality control testing for drug product release, stability, and lentiviral batch identification. Ensures GMP compliance while supporting lab operations and data integrity.

Senior Principal Scientist, Biostatistics, leads the implementation of innovative statistical approaches across the development portfolio. Responsibilities include developing designs, running simulations, and collaborating with partners. Requires Ph.D. or Master's with 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.

Senior Manager Parenteral and Liquids Development advances formulation and process development for small molecules and peptides. This role guides programs from discovery through commercialization, managing technology transfers and regulatory submissions.