Life Sciences Consultancy & Project Management in Netherlands

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…

The Company A leading organization in the life sciences and pharmaceutical manufacturing sector focused on producing high quality products in a highly regulated environment. The company operates under strict quality and compliance standards, ensuring patient safety and regulatory excellence through robust GMP practices. Role description As a Quality Operations Documentation Specialist I, you will play a key role in ensuring the accuracy, control, and compliance of GMP documentation used throughout manufacturing operations. The position focuses on the issuance, verification, and management of controlled documents, labels, and logbooks while supporting continuous improvement initiatives and maintaining regulatory compliance. Responsibilities – Verify controlled issued batch documents and label packages, including final product labels, in accordance with cGMP requirements – Verify controlled issued logbooks for accuracy and completeness – Ensure timely consumption of GMP materials and consumables or communicate inventory requirements to responsible personnel – Maintain accuracy and completeness of QA issued documents – Identify and escalate compliance gaps within the controlled issuance process – Support process improvement initiatives related to document control and issuance – Investigate and support deviations related to controlled issuance…

The Company Our client is a well-known global dairy cooperative with over 150 years of experience in delivering high-quality dairy products and nutritional solutions worldwide. Role Description As a Customer QA Manager, you’ll act as the key quality partner for customers, managing complex quality topics and translating customer requirements into practical internal solutions. You’ll work closely with QA, R&D, Regulatory, Operations and Sales while driving customer satisfaction and continuous improvement. Responsibilities – Serve as the main point of contact for customer quality inquiries and issues – Lead and coordinate complex customer cases and quality requests – Translate customer quality requirements into internal standards and ensure alignment across Operations, R&D, Regulatory, and Sales teams – Build and maintain strong relationships with key customer stakeholders to foster long-term partnerships based on trust – Ensure products and processes meet internal standards, regulatory requirements, and customer expectations – Analyse customer feedback and quality data to identify trends and implement continuous improvements – Drive initiatives for quality assurance and innovation based on customer insights Requirements – Master’s degree in Food Technology, Life Sciences, or a…

Company Our client is a global organisation operating in a highly regulated pharmaceutical manufacturing environment. The site combines production and quality expertise to ensure products are made safely, consistently, and in full compliance with GMP and internal quality standards. The culture values ownership, clear documentation, and practical collaboration between Quality and Production. Job Description We are looking for a Deviation Investigator to support a production organisation by managing deviations and leading quality investigations to timely closure. The focus of this role is on quality-system investigations rather than routine production work. The successful candidate will be analytical, structured, and confident working independently while partnering closely with Production stakeholders. Responsibilities – Write, manage, and coordinate deviations from start to closure. – Lead quality investigations, including defining scope, gathering evidence, and documenting findings. – Perform root cause analysis and support the definition and follow-up of corrective and preventive actions (CAPAs). – Work closely with Production teams to clarify facts, challenge assumptions when needed, and keep investigations moving. – Ensure investigation files are complete, traceable, and compliant with GMP and internal quality standards. – Review…