553 English-speaking jobs in Antwerp Province

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.

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.

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/Principal Scientist needed for mass spectrometry of advanced synthetic modalities, focusing on ADCs and tLNPs. Develop high-resolution MS methods for structure elucidation and lead root cause investigations.

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.

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.

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.

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.

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.

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.

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.

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.

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, safety, and compliance of investigational medicines by investigating complaints and logistics issues across global teams.

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 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 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.

This early career Project Manager PMO & Data Governance role coordinates site-wide initiatives, strengthens project governance, and standardizes PM practices. Responsibilities include S&OP management, driving change, and designing data solutions.

Principal in Health Economics and Health Technology Assessment, delivering client service and building trusted relationships. Focus on developing business opportunities and delivering high-impact consulting engagements for life sciences clients.

Drive international growth by selling MES-systems to B2B customers in global textile and plastics markets. Requires technical background and 10 years of sales experience, with fluency in English.