The Company A global technology and innovation driven organization focused on advancing healthcare, digital solutions, and consumer products. The company operates across multiple international markets and brings together expertise in engineering, artificial intelligence, product development, and regulatory excellence to deliver impactful solutions. Role description The Senior Innovation Project Manager leads strategic and highly complex innovation programs from concept through market launch. This role drives the development of advanced medical devices, digital health platforms, AI enabled solutions, and consumer technologies while coordinating cross functional teams across multiple locations. The position combines strategic leadership with hands on program execution in a highly regulated environment. Responsibilities – Lead large scale innovation programs across multiple business units and functions – Drive end to end product realization from concept development through launch and lifecycle management – Define program scope, architecture, value creation strategies, timelines, budgets, and risk management plans – Coordinate teams across engineering, software, artificial intelligence, design, regulatory affairs, manufacturing, and supply chain – Ensure compliance with quality systems, product safety requirements, and global regulatory standards – Oversee program governance activities, executive reporting, and…

The Company Our client is a leading biotechnology company dedicated to serving patients worldwide. With a strong focus on innovation and quality, they operate a global network that ensures medicines are reliably produced, tested, and distributed. Their culture is built on values, continuous development, and empowering their teams to make a meaningful impact. Job Description We are recruiting for a Quality Assurance Specialist – Qualified Person to join their site in Breda. The role involves ensuring that medicinal products meet all regulatory standards before they are released, supporting the company’s commitment to high-quality medicines, and contributing to continuous improvement initiatives within the QA team. Responsibilities – Certify batches of medicinal products and investigational medicinal products in compliance with EU and international regulations. – Collaborate with production, warehouse, distribution, and supply chain teams to ensure adherence to quality policies and procedures. – Act as the primary QA contact for deviations and CAPAs, ensuring investigations and resolutions meet regulatory standards. – Write, review, and approve quality procedures and job aids, ensuring they align with corporate and regulatory requirements. – Support and lead…

The Company A leading biopharmaceutical manufacturing organization focused on the development and production of high-quality biologic medicines. The company operates in a highly regulated environment and is committed to innovation, quality, compliance, and continuous improvement across its manufacturing processes. About the Role We are seeking an Engineer MSAT Validation to support process validation activities within biologics drug substance manufacturing. This role focuses on ensuring manufacturing processes are validated, compliant with regulatory requirements, and optimized for commercial production. You will work closely with technical, quality, and manufacturing teams to execute validation projects and drive operational excellence. Responsibilities -Plan, coordinate, and execute supporting process validation activities -Conduct mixing validation, buffer hold time validation, microbial hold time validation, and moist heat sterilization qualification -Prepare, review, and maintain validation protocols, reports, and support documentation -Support validation and qualification activities for both new and existing manufacturing processes -Execute performance qualification activities related to change controls and improvement projects -Collaborate with cross functional teams to deliver validation activities according to project timelines -Ensure compliance with GMP requirements and ALCOA plus data integrity principles -Identify opportunities for…

Company A leading organization dedicated to maintaining high standards in food safety, quality, and sustainability. The company continuously strives to ensure that its products adhere to strict regulations while fostering a culture of ongoing improvement and excellence in food production. Job Description We are seeking a knowledgeable and proactive Food Safety and Quality Improvement Specialist to join our client’s team. The successful candidate will oversee the adherence to food safety and quality standards, drive process improvements, and support certification compliance across production operations. Responsibilities -Ensure compliance with all relevant food safety, quality, and environmental regulations, as well as internal standards. -Maintain, monitor, and continuously enhance the Quality Management System (QMS) and related processes. -Lead and participate in internal and external audits, managing preparation, execution, and follow-up actions. -Oversee certification requirements such as IFS, HACCP, RSPO, and Beter Leven, ensuring timely renewal and compliance. -Serve as the primary point of contact and consultative partner for the QE Manager and production leadership on quality and process issues. -Initiate, coordinate, and support improvement projects aimed at elevating product quality and operational efficiency. -Perform…

Job Description We are seeking a motivated Cell Therapy Technician to support the production of clinical and commercial cell therapy products in a GMP-regulated aseptic manufacturing environment. In this role, you will collaborate with cross-functional teams to ensure safe, compliant, and efficient manufacturing while maintaining the highest quality standards. Key Responsibilities -Perform manufacturing activities, including aseptic processing, batch documentation, and sample handling. -Prepare growth media in cleanroom environments and carry out material decontamination procedures. -Complete and review batch records to ensure GMP compliance and accurate documentation. -Transfer samples for quality control analysis and perform cryopreservation of excess cells and finished products. -Assist with troubleshooting manufacturing equipment and recommend process improvements. -Participate in continuous improvement and change control initiatives. -Maintain cleanroom standards and ensure manufacturing workstations remain organized and compliant. -Work a rotating shift schedule, including mornings, evenings, and weekends, based on production Requirements -MLO, MBO, or HBO qualification (MBO Level+ or higher) in Life Sciences or a related discipline. -Experience working in a cGMP-regulated pharmaceutical, biotechnology, or similar manufacturing environment. -Understanding of biopharmaceutical manufacturing processes. -Practical experience with aseptic techniques…

The Company A manufacturing company that produces high quality products using advanced automated production systems. The company works in a GMP regulated environment where safety, quality, and compliance are very important. About the Role As an Automated Production Operator, you will run and monitor automated production machines to ensure products are made safely, efficiently, and according to quality standards. You will help solve machine issues, record production information, and support improvements to production processes. Responsibilities -Manage and monitor automated production equipment -Troubleshoot machine issues and make necessary adjustments -Record and verify production data in SAP and MES systems -Complete GMP documentation and maintain accurate production records -Work with Quality, Engineering, and Production teams to resolve issues -Perform equipment cleaning, basic maintenance, and production line setup -Support process improvements and continuous improvement initiatives -Ensure safe working practices and effective shift handovers Requirements -Minimum 3 years of experience in a similar production or manufacturing role -Experience working with automated production equipment -Experience in assembly and packaging processes is preferred -Good English communication skills -Comfortable following strict procedures and GMP requirements -Willing to…