121 English-speaking jobs in Breda

Lead CQV Engineer for Benelux projects. Lead technicians in qualification/calibration/automation I/O checks. Review CQV documentation and supervise field execution. Requires degree in Electrical/Instrumentation Engineering and 8+ years in Life Sciences.

This role leads supplier onboarding for the SmartEquip platform and provides ongoing support to fleets and suppliers. Responsibilities include coordinating implementation requirements and troubleshooting technical issues.

As a packaging operator, you will set up and monitor production lines for candy brands, ensuring quality standards are met. This role involves resolving minor technical issues and contributing to process optimization in a three-shift system.

Operate and monitor production and packaging equipment in a pharmaceutical manufacturing environment. Follow work instructions, SOPs, and safety procedures. Report deviations and technical issues. Experience in a manufacturing environment is preferred. Good communication skills in English are required. Willingness to work a 3-shift rotation.

Delivery Couriers pick up food from local restaurants and deliver it safely and on time using a bike or scooter. Must be at least 16 years old and available for at least two evenings per week.

Drive business development for fluid handling and heat exchanger products in the pharmaceutical industry. Focus on understanding customer needs, providing optimized solutions, and building strong relationships with key industry players.

As a Stock associate at Albert Heijn, you will assist with unloading trucks and stocking shelves. You will work with a team to ensure store orderliness and customer satisfaction.

Deliver groceries for Flink using electric bikes or scooters. Responsibilities include safe, timely deliveries and being active in the city hub. Must be at least 16, have valid work eligibility in the Netherlands, and speak English or Dutch.

Lead the strategic development and maintenance of Pharmanovia's global compliance, ethics, risk, and governance framework. Provide expert advice on complex regulatory matters across multiple jurisdictions.

Business Developer for Plugged Live Shows. Strategically respond to opportunities using industry knowledge and network. Set sales strategy for corporate, brand, and public events while building long-term client relationships.

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.

Lead the strategy and development of Facilities, Utilities, and Engineering for a GMP manufacturing site. Ensure critical infrastructure is safe, reliable, and compliant while driving operational excellence and growth.

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.

Coordinates Health, Safety, and Environmental activities across Belgium, Netherlands, and Luxembourg. Manages ISO 14001 and ISO 45001 compliance, conducts audits, and ensures adherence to legal and corporate EHS requirements.

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.

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.

QA Specialist provides quality oversight for equipment, automation, and information system validation and lifecycle management. Responsibilities include reviewing technical documentation and ensuring GMP compliance. Requires a Master's degree and 5-8 years of GMP 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.

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.