Life Sciences Consultancy & Project Management in Netherlands

Company A global, highly regulated manufacturing environment where quality, safety, and compliance are central to daily operations. The site works under strict GMP standards and follows detailed procedures to ensure reliable, audit-ready performance across production and support functions. Job Description For our client, we are looking for a Validation & Calibration Engineer to support validation and calibration activities on site. The role combines hands-on technical work with strong documentation responsibilities, ensuring equipment and processes remain compliant, accurate, and ready for inspection. Responsibilities – Execute validation and calibration activities in a GMP environment, following SOPs and work instructions. – Work with temperature measurements and process equipment, ensuring accurate results and traceable records. – Prepare and maintain clear technical documentation, including reports and supporting evidence. – Support compliant operation of site equipment and utilities by identifying issues, documenting findings, and following up on required actions. – Work independently on site while coordinating effectively with relevant stakeholders to keep work aligned and compliant. – Contribute to structured, accurate documentation in both Dutch and English, including Dutch-language procedures and reports. – Apply knowledge of…

Company Our client is a large, highly regulated organization within the pharmaceutical sector, operating a modern production site where quality, compliance, and safety are critical. The site works under GMP standards and relies on robust processes, clear documentation, and well-maintained equipment to ensure reliable operations. Job Description For an on-site role in Boxmeer (Netherlands), we are looking for a GMP Validation & Calibration Specialist who can independently support validation and calibration activities in a GMP environment. The GMP Validation & Calibration Specialist combines hands-on technical work with strong documentation skills, ensuring all work is executed in line with SOPs and work instructions and recorded accurately in both Dutch and English. Responsibilities Perform validation and calibration activities on-site within a GMP pharmaceutical environment. Work strictly according to SOPs and work instructions, ensuring consistent compliance. Prepare, maintain, and deliver clear technical documentation, reports, and records with a high level of accuracy. Support reliable and compliant operations by recording results precisely and following good documentation practices. Support activities involving temperature measurements and process equipment; autoclave-related knowledge is relevant to the work. Communicate effectively…

About the Company A global leader in pharmaceutical manufacturing, committed to delivering high-quality healthcare products that improve patients’ lives worldwide. The company operates within a highly regulated environment and is dedicated to maintaining the highest standards of quality, compliance, safety, and operational excellence. Role Description We are seeking a motivated and detail-oriented Pharmaceutical Manufacturing Associate to join a dynamic production team. In this role, you will be responsible for supporting manufacturing operations in a GMP-regulated environment, ensuring all production activities are carried out in accordance with approved procedures, quality standards, and safety requirements. Responsibilities – Execute manufacturing activities in accordance with Standard Operating Procedures (SOPs) and GMP regulations. – Perform manual production and operational tasks to support manufacturing processes. – Conduct in-process quality checks to ensure product quality and compliance. – Accurately complete batch records, logbooks, and production documentation. – Identify, report, and support the investigation of deviations and quality issues. – Assist with equipment preparation, setup, cleaning, and maintenance activities. – Support production changeovers and operational readiness activities. – Ensure the manufacturing area remains clean, organized, and audit-ready. – Follow…

The Company A large international organization operating across multiple markets with a strong focus on people development, digital transformation, and building future ready workforce capabilities. The organization is investing in digital learning, skills based development, leadership effectiveness, and modern talent solutions across its international workforce. About the Role We are looking for an Interim Digital Learning Manager within Learning and Development to lead several high-priority transformation initiatives. The primary focus is the Digital Learning Ecosystem, alongside a major enterprise Skills Programme. The role also leads the implementation of SHL development assessments and coordinates selected High Performing Team interventions across EMEA. This is a senior specialist position requiring strong L&D expertise combined with hands on experience in digital learning platforms and organizational development. Responsibilities Digital Learning Ecosystem -Lead the Learning and Development roadmap for the Digital Learning Ecosystem -Develop and drive the overall project plan together with Digital HR and internal L&D resources -Provide strategic direction and subject matter expertise from an L&D perspective -Lead implementation and continuous improvement of learning technologies and digital learning experiences -Improve learner experience, accessibility, engagement,…

The Company An international organization operating in the food and manufacturing sector, with a strong focus on safe production, operational excellence and continuous improvement. The Borculo site offers a hands on industrial environment where safety management and effective collaboration across operational teams are key priorities. About the Role We are looking for an experienced SHE Specialist for a temporary assignment in Borculo. The key objective is to further develop and implement the site Safety Management System, with particular focus on Permit to Work, TRA, LOTOTO and LMRA. You will work closely with different departments to develop procedures and work instructions and translate safety requirements into practical implementation. You will also support training development and practical guidance around the digital Unite X work permit system. Responsibilities –  Further develop and implement the Safety Management System VBS –  Improve Permit to Work processes –  Improve and implement TRA, LOTOTO and LMRA practices –  Develop safety procedures and work instructions together with relevant departments –  Support implementation of ARIE related safety requirements –  Work with the external training provider to create training materials…

Company A fast-growing organisation in the life sciences sector, operating in a highly regulated environment. The company is focused on scientific innovation and relies on robust laboratory IT systems to support critical research and development activities. Teams work closely together on-site, with a strong emphasis on compliance, security, and continuous improvement. Job Description We are looking for a Laboratory IT Operations & Migration Specialist to support day-to-day laboratory IT operations and help deliver integration and migration activities as systems transition to new corporate standards. This role combines hands-on technical support with system lifecycle work, documentation, and security-focused activities in an on-site lab environment. Responsibilities – Support daily laboratory IT operations, including maintenance, user support, inventory, and lifecycle activities. – Execute defined procedures to support integration and migration activities during a transition to new standards. – Contribute to laboratory IT security activities and support the implementation of improvements within the IT engineering domain. – Collaborate with internal stakeholders and external vendors to troubleshoot issues and address operational needs. – Support delivery of IT solutions, including upgrades, migrations, and implementations in a…