Life Sciences Consultancy & Project Management in Netherlands

The Company A global pharmaceutical organization focused on science driven innovation, technology excellence, and high quality manufacturing. The company operates across international markets and collaborates closely with manufacturing sites, technical operations teams, and external manufacturing partners to deliver compliant and efficient product supply. Role description The Technology Transfer Program Manager is responsible for leading Small Molecule drug product technology transfer projects across manufacturing sites. The role provides end to end oversight of transfer execution, ensuring projects are delivered on time, within quality standards, and in compliance with GMP and regulatory requirements. This position works closely with internal stakeholders, manufacturing facilities, contract manufacturing organizations, and global teams to drive successful technology transfer outcomes while continuously improving transfer methodologies and governance processes. Responsibilities – Lead and coordinate multiple Small Molecule technology transfer projects simultaneously – Manage site to site transfer execution activities across manufacturing networks – Monitor project timelines, milestones, risks, and project performance metrics – Ensure transfers are completed according to quality, compliance, and regulatory requirements – Coordinate activities between donor and receiving manufacturing sites – Collaborate with Manufacturing, Quality, Regulatory,…

Company  A leading organization in the pharmaceutical industry dedicated to ensuring the highest quality standards in manufacturing and product development. The company operates under strict regulatory guidelines and values excellence, compliance, and continuous improvement. Role Description We are looking for an experienced Quality Assurance Specialist Qualified Person (QP) to oversee and ensure the quality and regulatory compliance of pharmaceutical products. This role involves coordinating product release, managing quality investigations, and supporting inspections and audits to uphold the company’s high standards in production. Responsibilities – Review and approve master documents and specifications to ensure compliance – Initiate and evaluate quality investigations, making release or rejection decisions, and implementing improvement actions – Complete deviation and investigation reports promptly and accurately – Lead quality improvement initiatives to mitigate risks in production processes – Authorize ongoing stability studies and product quality reviews – Prepare for and manage inspections by government agencies and customers, including self-inspections and participation in overseas audits – Handle product complaints, investigate causes, and coordinate recalls when necessary – Maintain communication with external regulators, clients, and partners – Support technology transfer…

Company  Our client is a well-established, international food production and ingredients organisation with multiple manufacturing sites in Europe. They operate in a fast-paced supply chain environment where service, quality, and continuity of production are critical. The culture is professional, collaborative, and focused on continuous improvement. Job Description  For our client, we are looking for a Materials Planner to lead a small European materials planning team and ensure the timely availability of raw and packaging materials for production. The Materials Planning Team Lead (SAP) balances day-to-day operational priorities with a more tactical, forward-looking approach, working closely with internal stakeholders and suppliers to protect supply continuity. Responsibilities  – Lead and support a small materials planning team responsible for raw and packaging material availability across multiple production sites. – Manage the end-to-end ordering process for materials, ensuring orders are placed accurately and on time. – Monitor and optimise inventory levels while supporting working capital targets. – Translate production plans into material requirements and adjust plans when schedules change. – Coordinate and resolve supplier-related issues, including delivery problems and purchase complaints. – Ensure accurate…

Company A leading organization in the pharmaceutical industry dedicated to the development and manufacturing of Small Molecule drug products. They prioritize innovation, quality, and regulatory compliance to deliver high-quality medicines to patients worldwide. Job Description We are seeking an experienced Senior Project Manager to lead and oversee large-scale Small Molecule drug product technology transfers across manufacturing sites. The role involves managing key projects from start to finish, ensuring timely complaints, and high-quality transfer execution to support the company’s strategic growth. Responsibilities -Lead multiple Small Molecule technology transfer projects, ensuring smooth site-to-site transfers. -Oversee project timelines, risks, and milestones via dashboards and reporting tools. -Collaborate closely with Manufacturing, Quality, Regulatory, Supply Chain, Procurement, and other teams to align project goals and resolve issues. -Develop and maintain project governance, provide best practices, and coach project teams and sponsors. -Act as the primary contact for manufacturing sites and global functions, fostering strong relationships and clear communication. -Support regulatory submissions related to transfers and ensure compliance with GMP standards. -Contribute to continuous improvement of transfer processes and methodologies, driving best practices across regions. -Provide…

Company Our client is a leading global pharmaceutical organization focused on innovation, scientific excellence, and the reliable delivery of high-quality medicines. The organization operates across international manufacturing sites and maintains strong standards for GMP, regulatory compliance, and operational excellence. Role Description As an Associate Director, Technology Transfer Execution, you are responsible for leading Small Molecule technology transfer projects across global manufacturing sites, managing transfer execution from planning through completion while ensuring projects are delivered on time, in compliance with GMP and regulatory requirements, and to the required quality standards. You will work closely with Manufacturing, Quality, Regulatory Affairs, Supply Chain, Technical teams, CMOs, and global stakeholders to ensure successful project execution and alignment. Responsibilities – Lead and coordinate multiple Small Molecule technology transfer projects across manufacturing sites. – Manage project timelines, milestones, risks, deliverables, and governance. – Coordinate activities between donor and receiving sites and ensure effective stakeholder alignment. – Work cross-functionally with Manufacturing, Quality, Regulatory, Supply Chain, and Technical teams. – Support GMP compliance, process validation, qualification, change controls, deviations, and regulatory documentation. – Act as a key contact…

Company Our client is a leading organization committed to maintaining the highest standards in quality and compliance within their regulated operations. They focus on ensuring safe and effective products through meticulous documentation and adherence to GMP guidelines. Role Description As a QA Documentation Specialist, you are responsible for verifying the accuracy and completeness of controlled batch documents and labels, ensuring compliance with quality standards and regulatory requirements, and supporting continuous improvement of documentation processes. Responsibilities – Verify controlled batch documents and label packages, including final product labels, in accordance with cGMP standards. – Confirm the accuracy and completeness of QA-issued documents and logbooks. – Ensure timely use and proper management of GMP materials and consumables, informing the responsible personnel as needed. – Identify and escalate compliance issues within the controlled issuance process. – Support initiatives aimed at improving documentation procedures. – Investigate deviations related to controlled document issuance and develop effective corrective action plans. – Perform additional duties as assigned, delegating tasks to qualified team members when necessary. – Prioritize tasks to meet deadlines, demonstrating strong attention to detail and…