613 English-speaking jobs in Antwerp Province

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.

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.

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.

Senior/Principal Scientist needed for mass spectrometry of advanced synthetic modalities like ADCs and tLNPs. Lead method development and root cause investigations for complex pharmaceutical ingredients.

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.

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.

Manager, Capacity Management shapes resource and capacity strategies across divisions by providing forward-looking insights for portfolio and workforce decisions. This role owns resource forecasting models and translates complex analyses into executive recommendations.

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.

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.

QC CAR-T Investigation Coordinator role supporting daily QC operations and leading investigations for CAR-T treatments. Requires a Master's/Bachelor's degree, cGMP knowledge, and weekend availability.

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.

Director, Clinical Data Transparency, EHDS Programme Management provides strategic and operational leadership for J&J Innovative Medicine's EHDS programme, defining strategy, governance, and implementation roadmaps.

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.

Serve as the subject matter expert for EU Medical Device and IVD Regulations within R&D Global Development. Lead regulatory impact assessments and drive compliance within the Clinical QMS. Requires 5+ years in relevant regulated environments.

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.

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.

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

Lead PSTS integration and transition management for acquisitions and transactions. Coordinate diligence findings into integration plans, manage risks, and ensure Day 1 readiness across functions. Requires 8+ years in life sciences.

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 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.