115 English-speaking jobs in Breda

Manual Operator in a pharmaceutical production environment performing manual production and packaging tasks. Responsibilities include monitoring quality, completing GMP documentation, and adhering to strict procedures. Requires accuracy, reliability, and English proficiency.

Production Operator to operate and monitor semi-automated production lines in a GMP environment. Responsibilities include machine setup, troubleshooting, and data recording via SAP/MES. Requires technical education and experience with automated production lines.

Join Flink as a Bike Courier for fast grocery deliveries. This flexible role offers part-time or full-time contracts. Must have valid Dutch work eligibility and speak English or Dutch.

Trade Compliance Mgr responsible for integrating import/export policy and execution. Manages operational activities, export controls, and sanctions compliance. Requires relevant experience and knowledge of customs regulations.

Lead the Utilities Maintenance team to ensure safe and reliable operation of critical utility systems like HVAC and refrigeration. Drive operational excellence and asset lifecycle planning in a manufacturing environment.

Shape the vision and roadmap for SD Worx's integration platform and API ecosystem. Drive API development, lead strategic integrations like Workday, and manage the transition from legacy capabilities.

Operator ensures industrial machines run smoothly in day shifts. Responsibilities include monitoring production lines, resolving minor technical issues, and tracking admin tasks. Requires practical knowledge of sensors and pneumatic systems.

EHS Specialist coordinates Health, Safety, and Environmental activities across Belgium, Netherlands, and Luxembourg. This role manages ISO 14001 and ISO 45001 compliance, conducts audits, and ensures adherence to legal requirements.

Packaging Operator in a pharmaceutical environment. Tasks include manual production, quality checking, and GMP documentation. Requires accuracy, reliability, and willingness to work in shifts. Good English is required.

Result-oriented Talent Acquisition Specialist managing end-to-end recruitment across the Netherlands. This role involves strategic workforce planning, stakeholder management, and international collaboration to attract technical talent.

Work as a flexible hospitality staff member in service, bar, or catering across the Breda, Tilburg, and Den Bosch region. Choose your shifts and hours between 4 and 40 per week. No prior experience is required.

This role manages test code configuration and maintains the CTMS Laboratory Services Catalog. Responsibilities include translating project needs into catalogue services and interfacing new tests between analyzers, middleware, and LIMS. Requires 2+ years in a diagnostic or clinical laboratory.

Ensure medical nutrition products are packed, labeled, and checked with precision. This role involves packaging, printing labels, and moving products up to 13 kg while collaborating with the team. Requires full-time availability and comfort with shift work.

Associate Supply Chain supports international pharmaceutical distribution by coordinating end-to-end shipments and managing import/export compliance. Requires a relevant degree and 2+ years of Supply Chain experience.

Sr QA Associate provides quality oversight for equipment, automation, and information system validation in a GMP environment. Requires a Master's degree and 5-8 years in pharmaceutical settings, with expertise in validation and risk management.

Senior Quality Validation Specialist provides QA oversight for equipment, automation, and information systems validation, and Quality Risk Management. Requires a Master's degree and 4-8 years in a GMP environment with validation and risk management experience.

Experienced QA Specialist needed to support quality oversight for equipment, automation, and information systems validation in a GMP environment. Responsibilities include protocol review, risk management, and change control assessment. Requires a Master's degree and 5-8 years in GMP.

Installation Engineer responsible for implementing, installing, and commissioning mechatronic systems and robotic solutions in laboratory automation. Requires a hands-on attitude and willingness to travel nationally and internationally.

QA Specialist provides oversight for equipment, automation, and information system validation, ensuring compliance with corporate and regulatory requirements. Responsibilities include reviewing validation documentation and supporting Quality Risk Management. Requires a Master's degree and 5-8 years of GMP experience.

Specialist QA role supporting validation of equipment, automation, and information systems in a pharmaceutical/biotechnology setting. Requires a Master's degree and 5-8 years of GMP experience.