674 English-speaking jobs in Antwerp Province

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 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.

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.

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.

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.

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.

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.

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 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.

MSAT Synthetics Drug Product External Site Principal Scientist provides technical oversight to external manufacturing sites. Responsibilities include NPI, tech transfers, and lifecycle management. Requires 8+ years experience with dosage forms and EM networks.

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.

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 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.

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 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.

Postdoctoral Scientist - AI/ML to advance AI/ML and generative AI for drug discovery. Responsibilities include developing foundation models for biological sequences and establishing lab-in-the-loop workflows. Requires expertise in modern AI/ML methods.

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.

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.

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.

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.