764 English-speaking jobs in Antwerp Province

Data Management Analyst (ERP) supports master data accuracy, setup, and integrity across business applications. Responsibilities include data quality monitoring, governance, and analyzing business requirements. Requires 2+ years in MDM or related data management.

Design Engineer needed for a deep tech firm specializing in high-end aluminum and steel curtain wall systems. Responsibilities include design detail preparation, BIM/3D drawing creation, and coordination. Requires a technical system planner apprenticeship and 2+ years in façade engineering with excellent CAD knowledge.

Experienced Data Platform Solution Architect & Engineer to advance an organization-wide Data Mesh. Responsibilities include advising on data technologies and building the core data stack using AWS, Airflow, Spark, Snowflake, and dbt.

Senior Product Manager to lead strategy and roadmap for a critical fitting platform. Own product direction, balancing customer needs, clinical insight, and business priorities to improve hearing outcomes.

(Senior) Scientist in API Particle Engineering Research will design and optimize crystalline particle attributes for robust, scalable Active Pharmaceutical Ingredients. This role requires expertise in crystallization, characterization, and process development.

Senior Scientist Material Sciences will provide expertise in selecting excipients for robust drug formulations. This role involves investigating physicochemical properties to enhance drug delivery and ensure supply chain robustness.

Junior QA Associate provides Quality Assurance oversight for Mobile Equipment Cleaning and acts as the primary Quality Point of Contact. The role ensures cGMP compliance while supporting operational departments and contributing to quality systems.

Principal Scientist (Manager), Global Regulatory Affairs, CMC develops global CMC regulatory strategies for large molecules in clinical and post-marketing stages. This role leads regulatory activities and prepares dossiers for Health Authorities.

(Senior) Scientist role in Precipitation & Particle Design Research focuses on engineering particle attributes of peptides for robust, scalable APIs. Responsibilities include designing precipitation and isolation processes using advanced analytical techniques.

Senior Principal Scientist/Principal Scientist in Scientific Integration drives analytical development strategies for Synthetic Modalities. This role acts as the CMC expert, ensuring scientific rigor and regulatory readiness across the product lifecycle.

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 Scientist in Analytical Development develops chromatographic test methods for APIs and impurities, focusing on LC-UV/MS. This laboratory role involves method development, validation, and managing projects in drug development.

Manager, Clinical Supply Chain Quality, acts as a Qualified Person delegate for certifying and releasing investigational medicinal products. This role ensures quality oversight across complex clinical supply chains, requiring a Pharmaceutical Sciences degree and EU-certified QP.

Manager, Trial Delivery Management executes study-level activities, manages vendors, and oversees regional operational delivery. This role involves creating trial documents, risk reviews, and supporting program training.

This role is a scientific authority ensuring a robust strategy on impurities in synthetic drug products, focusing on Nitrosamine Risk Assessment across the commercial portfolio. The Fellow provides technical continuity from development through commercial manufacturing.

QC Biotech Intern role offers hands-on lab experience supporting CAR-T cell therapy production. Responsibilities include analytical testing under GMP, data interpretation, and maintaining lab safety. Candidates should be enrolled in a scientific degree.

QA Release Responsible ensures quality oversight for incoming materials and supports EU Batch Release activities in a pharmaceutical manufacturing environment. This role requires maintaining GMP compliance and making risk-based quality decisions.

Manager, Serious Breach Office drives compliance for serious breach reporting in clinical trials. This role facilitates assessments, monitors process performance, and drives continual improvement within R&D Quality.

Director, IM R&D Procurement leads global category strategies for CMC Product Development and Clinical Manufacturing. This senior role drives value through strategic supplier relationships, risk management, and innovation across the Innovative Medicine portfolio.

Support daily QC operations and lead investigations for CAR-T treatments. Requires Master's/Bachelor's with relevant experience, knowledge of cGMP/FDA/EU guidance, and strong organizational skills.