Site HSE Advisor, Rotterdam, Zuid-Holland

Company Our client is a well-established organisation in the life sciences sector, working on research and development projects that support the creation, testing, and improvement of biological products. The environment is hands-on and collaborative, with strong focus on quality, accurate record-keeping, and working safely and consistently in the laboratory. Job Description We are looking for a Microbiology Technician to support a busy research laboratory in Boxmeer. The Laboratory Research Technician will work across different projects and activities, helping the team deliver reliable laboratory results and maintain accurate documentation. The work is fully on-site and requires flexibility, as the daily tasks can vary based on project needs. Responsibilities - Support laboratory research activities across multiple projects and teams - Perform sample processing and general laboratory tasks as required - Carry out testing activities such as immunoassays (e.g., ELISA/AlphaLISA) and other laboratory experiments - Support bacteriological and virological testing activities, depending on project requirements - Contribute to stability and potency testing activities for biological products - Assist with laboratory work connected to animal studies when needed - Record work accurately and maintain complete laboratory documentation and records - Work in a structured way, follow agreed procedures, and communicate clearly with colleagues and stakeholders Requirements - 2–4 years of relevant laboratory experience - Strong written and spoken Dutch (needed for laboratory documentation and records) - Available for 40 hours per week - Willing and able to work 100% on-site in Boxmeer (5 days per week) - Hands-on experience with one or more relevant techniques/activities such as: ELISA, AlphaLISA, virus titration, bacteriological/virological testing, sample processing, stability testing, or potency testing - Flexible mindset and comfortable working on changing priorities across different projects -Temporary Full-Time 12 Months Contract Other Information This role requires full-time, on-site availability in Boxmeer and offers the chance to contribute to varied laboratory activities in a dynamic research setting. If you are interested and want to apply, please submit your application via the apply button below and contact me.

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 autoclaves where relevant to validation/calibration activities. Requirements - Higher vocational level education (HBO) or equivalent. - Proven experience in a GMP/pharmaceutical manufacturing environment. - Hands-on experience with validation, calibration, and technical documentation. - Fluent Dutch (required) and good English skills. - Ability to work accurately, independently, and in a structured way. - Experience with autoclaves and/or process equipment and temperature measurements is a strong advantage. Other Information The work is performed fully on site in Boxmeer, and the interview process typically consists of 2 to 3 conversations, with a preference for face-to-face meetings.  

Company Our client is a leading organisation within a highly regulated manufacturing environment. The site operates complex production and utility systems and places strong emphasis on safety, quality, and reliable operations. The teams work closely together across production, engineering, and technical services to keep equipment available and maintenance activities well controlled Job Description For our client, we are looking for a Maintenance Work Preparation Coordinator who will prepare and plan preventive and corrective maintenance activities for technicians on site. The role focuses on creating safe, efficient, and well-documented maintenance plans, coordinating permits, and aligning work with production to minimise disruption. Responsibilities - Prepare, prioritise, and plan preventive and corrective maintenance work. - Create and coordinate work permits and required safety documentation, including lock-out/tag-out procedures. - Ensure equipment can be safely shut down and made ready before maintenance activities begin. - Prepare clear work packages, job descriptions, instructions, and supporting documentation for technicians. - Coordinate schedules and align maintenance activities with production planning and site stakeholders. - Arrange required materials, spare parts, tools, and internal/external resources to execute planned work. - Maintain clear communication between technical teams, production, and external parties when needed. - Follow up on progress and support proper documentation and closure of completed maintenance activities. - Support shutdowns, modifications, and improvement initiatives by coordinating preparation and planning. Requirements - Fluent in Dutch (spoken and written). - Experience in maintenance planning and/or work preparation in an industrial production environment. - Strong understanding of work permit processes and safe isolation procedures (lock-out/tag-out). - Technical education at MBO+/HBO level, preferably in Mechanical, Electrical, Automation, or similar. - Strong organisational skills and the ability to coordinate multiple stakeholders. - Clear communication style and a practical, hands-on mindset. - Experience in a regulated environment (e.g., GMP) is a strong advantage. -Temporary Full-Time Contract - 12 Months Other Information The position is fully on-site and involves close collaboration with production and technical teams. The hiring process may include up to two interviews, with on-site meetings preferred. If you are interested and want to apply, please submit your application via the apply button below and contact me.

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 in both Dutch and English, including working with Dutch-language procedures and documentation. Requirements Completed HBO-level education (or equivalent). Proven experience in a GMP/pharmaceutical environment. Hands-on experience with validation, calibration, and technical documentation/reporting. Fluent Dutch (required) and strong English skills (spoken and written). Able to work accurately and independently, with enough experience to be productive quickly in an autonomous role. Nice to have experience with autoclaves, temperature measurements, and process equipment. Other Information: If you are interested and want to apply, please submit your application via the apply button below and contact me.  

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 all safety, quality, and compliance requirements at all times. - Collaborate with Production, Quality Assurance, and other cross-functional teams to achieve operational goals. - Participate in continuous improvement initiatives and team meetings. - Maintain a proactive approach to problem-solving and operational efficiency. Requirements - Minimum 2 years of experience operating manual and/or semi-automated production lines within a manufacturing environment. - Experience working within a GMP-regulated environment is highly preferred. - Good understanding of manufacturing processes, SOPs, and quality standards. - Fluent in English, both written and verbal. - Strong attention to detail and commitment to quality. - Ability to work effectively in a structured and process-driven environment. - Comfortable performing repetitive tasks with accuracy and consistency. - Strong teamwork and communication skills. - Willingness to work in a shift operation.  Other Information If you are interested and want to apply, please submit your application via the apply button below and contact me.

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, and adoption -Manage collaboration with Digital HR, internal stakeholders, and technology vendors -Align the digital learning ecosystem with enterprise capability priorities -Provide direction on the effective use and development of learning experience platforms Skills Agenda -Act as the Learning and Development lead within the enterprise Skills Programme -Translate organizational skills requirements into practical learning, upskilling, and reskilling initiatives -Represent L&D requirements in decisions concerning skills governance, taxonomy, architecture, and operating models -Connect skills intelligence with workforce capability requirements and learning solutions -Support the organization's transition towards a skills based approach to workforce development High Performing Teams -Manage incoming requests relating to High Performing Team interventions across EMEA -Advise stakeholders on the most appropriate solutions and resources -Support facilitators throughout intake, scoping, delivery, and evaluation -Coordinate interventions across the EMEA region -Work with business leaders, HR Business Partners, facilitators, and external providers -Monitor implementation and follow through on agreed actions SHL Assessment Implementation -Lead implementation, rollout, and adoption of SHL development assessment solutions -Support the transition from the existing assessment solution -Update development assessment policies, governance, communications, and supporting materials -Manage 360 assessment design and competency mapping -Support stakeholder engagement and enablement -Integrate SHL assessment solutions into broader employee development processes -Use pilot outcomes to support implementation recommendations and future improvements Requirements -Significant professional experience within Learning and Development -Strong experience with digital learning platforms and learning technologies -Hands on LXP experience -Experience leading digital learning ecosystem initiatives -Strong Organizational Development expertise -Experience translating skills strategies into learning and capability solutions -Knowledge of skills taxonomy, skills architecture, or skills based workforce approaches -Experience managing complex stakeholders across HR, Digital HR, business teams, and external vendors -Experience with assessment solutions such as SHL is highly valuable -Experience with development assessments and 360 assessments is advantageous -Strong project leadership and implementation capabilities -Ability to provide strategic direction while remaining hands on with delivery -Experience working within a large international organization -Strong English communication skills -SAP knowledge is a strong advantage The ideal candidate is a senior L&D specialist with digital platform expertise rather than a traditional Training Manager or general Program Manager. Other Information If you are interested and want to apply, please submit your application via the apply button below and contact me.

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 and OPLs -  Provide practical guidance and support to employees using the Unite X digital work permit system -  Work closely with stakeholders from the shopfloor through to management -  Support the practical implementation of improved safety processes across the Borculo site Requirements -  Completed higher professional education in a technical discipline -  HVK qualification -  Minimum 4 years of experience in a comparable SHE or safety position -  Current knowledge of ARIE legislation and Safety Management Systems -  Strong knowledge of Permit to Work, TRA, LOTOTO and LMRA -  Hands on and proactive approach -  Strong problem solving skills -  Able to work independently and as part of a team -  Strong stakeholder and communication skills -  Able to engage effectively with both shopfloor employees and management -  Good written and spoken Dutch -  Good written and spoken English -  Knowledge of Unite X is preferred Other Information If you are interested and want to apply, please submit your application via the apply button below and contact me.  

Company For a leading international organisation in the food and nutrition sector, we are looking for an experienced supply chain professional to support planning and integration activities across multiple production sites. The environment is dynamic and matrix-driven, with close collaboration between local teams, global planning, commercial stakeholders, and strategy. Job Description The Supply Planning Integration Lead (S&OP / MRP) will support and lead the integration of a supply network into end-to-end planning processes, including supply planning, scheduling and MRP. The role combines hands-on operational planning over a 13-week horizon with tactical planning over an 18-month horizon and helps translate a new product strategy into practical supply chain ways of working. The working location will be a mix of office and factory environments, with collaboration across sites in the Netherlands and Belgium. Responsibilities Lead and support the integration of a new network into supply planning, scheduling, and MRP processes. Drive alignment of multiple sites and stakeholders within the S&OP cycle, ensuring clear planning decisions and follow-through. Translate strategic objectives into workable planning processes and routines that teams can adopt. Work closely with supply planners and local supply teams to manage operational planning across a 13-week horizon. Support tactical planning across an 18-month horizon, linking capacity, demand, and supply plans. Coordinate with global S&OP, commercial and strategy stakeholders in a matrix organisation. Support project execution by setting clear frameworks, engaging stakeholders, and driving actions to completion. Requirements Bachelor’s or master’s degree, preferably in Supply Chain Management (or similar). Strong understanding of S&OP and planning principles (e.g., Rough-Cut Capacity Planning, MPS, MRP). Proven experience in supply chain projects, network integrations, and/or transformation programmes. Comfortable working cross-functionally in a matrix environment, across different organisational levels. Strong analytical skills and structured decision-making. Excellent communication skills and ability to bring stakeholders along. Fluent in English; Dutch is a strong advantage. Willingness to travel occasionally to sites in the Netherlands and Belgium. Other Information If you are interested and want to apply, please submit your application via the apply button below and contact me.  

The Company A large international organization operating a complex production environment with a strong focus on operational safety, compliance, and continuous improvement. The site works with structured safety management processes and digital systems to maintain high standards across daily operations. About the Role We are looking for an experienced SHE Specialist for a temporary assignment in Borculo. The main objective is to further develop and implement the Safety Management System, with particular attention to Work Permits, TRA, LOTOTO, LMRA, and ARIE requirements. You will work closely with operational departments and an external training supplier to develop procedures, work instructions, training materials, and practical implementation guidance. Responsibilities - Further develop and implement the Safety Management System at the Borculo site - Improve Work Permit processes, TRA, LOTOTO, and LMRA practices - Support the use and improvement of the Unite X digital Work Permit system - Develop safety training materials and OPLs together with the training supplier - Provide practical guidance to employees during implementation - Draft and implement ARIE related procedures and work instructions - Work closely with departments to ensure safety procedures are practical and effective - Engage stakeholders ranging from shop floor employees to management - Support continuous improvement of SHE processes and safety standards Requirements - Completed HBO level technical education supplemented with HVK - Minimum 4 years of experience in a comparable SHE, HSE, or safety position - Current and practical knowledge of ARIE legislation and Safety Management Systems - Strong knowledge of relevant safety legislation and regulations - Experience with Work Permits and risk assessment processes - Knowledge of TRA, LOTOTO, and LMRA - Hands on and proactive working style - Able to work independently while collaborating effectively with a wider team - Strong communication and stakeholder management skills - Able to communicate effectively from shop floor to management level - Good command of Dutch and English, both written and spoken - Knowledge of Unite X is an advantage Other Information If you are interested and want to apply, please submit your application via the apply button below and contact me.

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 regulated environment. - Maintain and update documentation and records (e.g., configuration and asset information, operating procedures, and work instructions). - Gather operational data, identify risks and improvement opportunities, and support reporting on performance and progress. - Provide clear status updates and present results in team or project meetings. Requirements - Bachelor’s degree in Computer Science, Engineering, or a related technical field. - 3+ years of experience in an IT engineering/operations role, ideally in a laboratory or regulated environment. - Experience supporting IT processes and participating in IT projects (e.g., upgrades, migrations, implementations). - Working knowledge of regulated ways of working and documentation practices (e.g., GLP/GxP, GDPR). - Strong analytical and problem-solving skills, able to work independently on assigned activities. - Clear communication skills and confidence working with both internal teams and external vendors. Other Information This is an on-site role within a laboratory environment, working closely with project teams and stakeholders to support operational continuity and migration activities. If you are interested and want to apply, please submit your application via the apply button below and contact me.