Company A leading pharmaceutical manufacturing company dedicated to producing sterile medicines. The organization specializes in mixing antigens and oils in large vessels and is committed to maintaining the highest standards of quality and safety throughout its production processes. Job Description We are seeking a Senior Validation Specialist to support a key project focused on validating and improving sterilization processes. The successful candidate will play a crucial role in investigating filtration methods to ensure they meet stringent sterilization requirements, ultimately enhancing the safety and efficacy of the products. Responsibilities – Investigate existing filtration processes to identify issues with current filtration efficiency. – Modify and optimize the filtration procedures to meet sterilization standards. – Write detailed protocols, statements, and validation reports in compliance with GMP requirements. – Collaborate with multidisciplinary teams on-site to execute validation activities. – Ensure all documentation and processes align with industry and internal quality standards. – Contribute to the ongoing improvement of sterilization validation projects. Requirements – Minimum of 5–6 years’ experience in the pharmaceutical or biotech sector, particularly in validation or sterilization processes. – Proven ability to…

Technical Operator (Automated Lines) About the Role We are looking for experienced Technical Operators to operate, monitor, and optimize highly automated production lines in a GMP-regulated manufacturing environment. You will ensure efficient production, maintain equipment performance, troubleshoot technical issues, and contribute to continuous improvement initiatives. Key Responsibilities Operate automated production equipment following SOPs and GMP standards. Perform troubleshooting, root cause analysis, and optimize machine settings. Record production data using SAP/MES systems. Complete GMP documentation accurately. Participate in QA, Maintenance & Engineering, and Production triage meetings. Perform equipment setup, shutdown, and routine cleaning. Support Lean and Continuous Improvement initiatives. Ensure safe working practices and effective shift handovers. Requirements Minimum 3 years of experience in automated manufacturing. Experience in pharmaceutical, biotech, food, or FMCG manufacturing preferred. Knowledge of GMP, SOPs, SAP/MES, Lean, Six Sigma, RCA, 5 Why, TPM, SMED, Kaizen, and Poka-Yoke. Technical qualification (MBO, VAPRO B, or equivalent). Knowledge of mechatronics, pneumatics, and electronics. Fluent in English and willing to work shifts. Apply Now If you have a strong technical background and enjoy working with automated production systems, we encourage you…

Company Our client is a large, international manufacturing organisation operating in a regulated, fast-paced environment. The site is part of a wider network of production locations and is currently preparing for a major digital transformation programme impacting core operational and support processes. Job Description For our client, we are looking for a SAP Implementation Lead (Manufacturing) who will take ownership of site deployment readiness for a major ERP transformation. This person will act as the single point of coordination on the plant site, aligning multiple departments and ensuring the organisation is prepared for testing, training, and cutover activities leading up to go-live. Responsibilities – Own overall deployment readiness for the site and keep activities on track across all local workstreams. – Coordinate local execution across functions such as production, maintenance, quality, planning, logistics, and finance. – Drive and support testing activities, ensuring the right people are involved and actions are followed up. – Coordinate training readiness, including alignment with key users and ensuring work instructions are prepared and embedded. – Manage and monitor risks, issues, and dependencies, escalating when needed…

Company Overview: A leading pharmaceutical organization focused on the production of sterile medicines. They operate state-of-the-art facilities and are committed to maintaining the highest standards of quality and safety in their products. Job Description: We are seeking a skilled Validation Specialist to support the validation of sterilization processes. This is a project-based role based in Boxmeer, designed to ensure that filtration and sterilization methods meet strict industry standards. The successful candidate will play a vital part in investigating and optimizing filtration techniques to address current challenges with filter performance. Responsibilities: -investigate existing filtration processes used during sterilization. -Modify and improve filtration methods to ensure they meet sterilization  requirements. -Write validation protocols, reports, and statements to document findings and procedures. -Collaborate with cross-functional teams on-site to implement process modifications. -Ensure all activities comply with GMP guidelines and quality standards. -Support validation activities from initial assessment through to final implementation. Requirements: -Minimum of 5–6 years of experience in the pharmaceutical sector. -Proven experience in writing protocols, validation reports, and technical documentation. -Strong knowledge of GMP regulations, sterilization, and filtration processes. -Solid understanding…

Company Overview Our client is a leading manufacturing organization focused on creating sustainable solutions that improve lives around the world. They prioritize safety and innovation, fostering a work environment that values continuous improvement and teamwork. Job Description We are seeking a dedicated Warehouse Operations Supervisor to oversee the storage and logistics processes at their Dordrecht location. This role involves leading a team responsible for managing materials, ensuring safety standards, and enhancing operational efficiency within the warehouse and support facilities. Responsibilities -Lead and support the team responsible for managing Maintenance, Repair, and Operations (MRO) goods, including inspection, storage, and issuing of materials in accordance with safety and operational standards. -Oversee the processes of kitting and staging materials, preparing shipments according to work orders. -Supervise safety equipment management, including inspection, repair, cleaning of safety apparel, filling air cylinders, and maintaining emergency mask sets. -Manage facility services such as handling internal and external mail, photocopying, and external printing services. -Ensure all activities adhere to safety procedures and company standards, conducting regular checks and audits. -Drive continuous process improvements to optimize team effectiveness and…

The Company A global leader in life sciences manufacturing that focuses on innovative engineering solutions and high quality production environments. The organization operates large scale capital investment projects and emphasizes safety, compliance, and continuous improvement across its global facilities. Role Description This is a senior level Project Manager position within a global engineering team, responsible for delivering large capital investment projects in a regulated manufacturing environment. You will independently lead complex engineering initiatives from concept through completion, ensuring projects are executed safely, on time, and within budget. The role requires strong leadership, stakeholder management, and hands on experience managing multi million euro projects across the full lifecycle. Responsibilities – Lead medium to high value capital projects from initiation to financial close out – Deliver projects in line with safety, quality, timeline, and budget expectations – Build and manage high performing cross functional project teams – Coordinate with internal stakeholders, contractors, suppliers, and engineering partners – Define project scope, timelines, budgets, and execution strategies – Manage governance, stage gate processes, and engineering standards – Oversee cost control, risk management, and change…