384 English-speaking jobs in Antwerp Province

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 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.

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 in Parenteral and Liquids Development designs formulations and processes for small molecules and peptides from discovery through commercialization. This role advances drug delivery and manages programs to regulatory submission.

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.

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.

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.

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.

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.

Senior ML Engineer for Biologics Discovery. Own deployment, lifecycle management, and governance of ML/AI solutions to enable reliable, production-grade AI workflows for scientific discovery. Requires 4+ years operationalizing AI/ML.

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.

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.

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.

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.

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 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.

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.

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.

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.