Financial Analyst, Rotterdam, Zuid-Holland

The Company A leading organization in the pharmaceutical manufacturing industry, committed to maintaining the highest quality standards in its production processes. The company values precision, compliance, and continuous improvement to ensure the safety and efficacy of its products. Role Description We are seeking a proactive and detail-oriented Quality Assurance Officer to join the GMP manufacturing team. This role is vital in ensuring that the packaging, labeling, and production processes meet strict quality and regulatory standards. The successful candidate will play a key part in maintaining quality, supporting compliance, and resolving issues in a fast-paced production environment. Responsibilities -Conduct final quality verification for all packaging and labeling orders before release. -Review batch records and documentation to ensure data accuracy, compliance, and completeness. -Manage and resolve deviations or quality issues during production. Investigate, document, and follow up on deviations or non-compliance issues. -Collaborate closely with Production, Maintenance, QA colleagues, and other departments to ensure smooth operations. -Exercise escalation authority by stopping production if quality or compliance concerns arise. -Provide guidance and support to production staff on GMP standards and procedures. -Review and approve batch production records and deviation reports. Requirements -MBO or BSc degree in Pharmaceutical Sciences, Life Sciences, or a related field. At least 3 years of experience in Quality Assurance or manufacturing within the ---pharmaceutical or medical device sector, with a focus on batch record review and investigations. -Strong understanding of GMP, GDP, and GCP regulations, with the ability to interpret and apply them. -Proven attention to detail and a methodical approach to quality and compliance tasks. -Skilled team player with excellent communication skills and the confidence to challenge production when necessary. -Fluency in English. -Valid driver’s license is a plus. Other Information This role operates on a three-shift system, involving early, late, and night shifts, with no rotation. Shift hours are as follows:

About the Company Join a leading manufacturing organization where operational excellence, collaboration, and continuous improvement are key to delivering high-quality products. In this role, you will lead a production team, support employee development, and help drive a safe, efficient, and high-performing manufacturing environment. Role Description As an Operations Team Lead, you will be responsible for leading and developing a manufacturing operations team while ensuring daily production activities are executed safely, efficiently, and in line with quality standards. You will provide technical guidance, coach team members, and collaborate closely with cross-functional departments to optimize processes and build a culture of continuous improvement. Key Responsibilities Lead, coach, and develop production, maintenance, and support personnel Provide technical expertise and day-to-day operational leadership within the manufacturing environment Ensure safe, efficient, and compliant execution of production activities Support team development through coaching, training, and performance management Foster a culture of continuous improvement, collaboration, and open communication Maximize the potential of team members through ongoing development and constructive feedback Ensure employees have the appropriate tools, resources, and training to perform their roles successfully Collaborate with cross-functional teams to improve operational performance and resolve production challenges Support process improvements and contribute to operational excellence initiatives Monitor team performance and help achieve production, quality, and safety objectives Promote a positive working environment focused on accountability, engagement, and teamwork Requirements Bachelor's degree or equivalent working and thinking level is preferred Experience leading teams within a manufacturing or production environment Strong leadership and people development skills Experience coaching, mentoring, and training employees Excellent written and verbal communication skills Ability to work effectively with cross-functional teams and stakeholders Strong organizational and problem-solving skills Proactive mindset with a focus on continuous improvement Ability to motivate and develop high-performing teams Comfortable working in a dynamic manufacturing environment with changing priorities

Company: A leading global consumer goods company renowned for its diverse range of brands in Food, Home, and Personal Care. Operating in over 190 countries, the company reaches billions of consumers daily through trusted brands in households worldwide. Job Description: We are seeking a motivated Financial Planning & Analysis Specialist to join a dynamic team supporting the Food division. This role involves partnering with various departments, driving financial insights, and contributing to strategic decision-making in the Benelux region. Responsibilities: •    Co-own and support the Sales & Operations Forecasting, Planning, and Value Cash Up processes for the Benelux Food division. •    Assist in month-end closing activities, providing insights and commentary for reports. •    Lead or support agile projects focused on adding value across the finance function. •    Contribute to the performance review processes, supporting strategic initiatives and financial interventions. •    Collaborate with cross-functional teams to identify risks and opportunities in the Profit & Loss statement. •    Support business performance reviews, helping to drive continuous improvement in financial results. •    Present complex financial information clearly to senior stakeholders and non-finance partners. •    Ensure all financial data and reports are accurate, insightful, and aligned with company standards. Requirements: •    Degree in Finance, Accounting, or related field; proven experience in financial analysis or business partnering. •    Experience working with departments like Marketing and Sales. •    Strong commercial awareness, analytical capability, and decision-making skills. •    Excellent communication skills, fluent in English (reading and writing). •    Proven ability to manage stakeholders and communicate financial insights effectively. •    Experience in creating financial models and delivering presentations with attention to detail. •    Resilience, flexibility, and a proactive approach to work and problem-solving. Other Information: If you are interested and want to apply, please submit your application via the apply button below and contact me. This role is based in the Netherlands and requires approximately 40% attendance at the office.

About the Company Join a global pharmaceutical organization where supply chain excellence plays a critical role in ensuring patients worldwide have access to life-saving medicines. Within an international and highly regulated environment, you will collaborate with colleagues across supply chain, logistics, quality, manufacturing, affiliates, and external partners to ensure reliable and compliant product distribution. Role Description As an Associate Supply Chain Import/Export Specialist, you will be responsible for coordinating end-to-end Order-to-Invoice activities for global pharmaceutical supply operations. You will manage import and export processes, coordinate shipments, resolve logistics issues, and ensure products are delivered to internal and external customers according to quality, regulatory, and customer requirements. Working within a GMP/GDP environment, you will act as a key link between supply chain teams, logistics partners, affiliates, and distributors while contributing to continuous improvement initiatives. Key Responsibilities Coordinate end-to-end shipments of pharmaceutical products to internal and external customers worldwide Execute daily supply order processing activities and ensure timely order fulfillment Manage import and export documentation according to regulatory and customer requirements Book, monitor, and follow up on shipments while proactively identifying potential delays or risks Resolve transportation, logistics, and service-related issues in collaboration with internal and external stakeholders Coordinate product return processes and ensure correct execution Collaborate with third-party logistics providers and supply chain partners Maintain strong relationships with affiliates, distributors, manufacturing sites, and internal departments Participate in cross-functional projects and represent the supply chain team Identify opportunities for process improvements within Order-to-Cash and logistics processes Support KPI reporting and provide insights for operational performance improvements Ensure compliance with GMP/GDP requirements, procedures, and required training Requirements Bachelor’s or Master’s degree in Supply Chain, Logistics, Business Administration, or a related field Minimum 2 years of Supply Chain experience within a GMP and/or GDP regulated environment Experience with import/export processes, logistics coordination, or customer service within supply chain is preferred Experience working with ERP systems and supply chain tools Strong affinity with systems, data, and administrative processes Experience handling logistics issues and solving operational challenges Strong organizational skills with the ability to manage multiple priorities Detail-oriented mindset with a strong focus on quality and compliance Customer-focused approach with strong stakeholder management skills Ability to work effectively within international and multicultural teams Excellent communication skills in English, both written and verbal

About the Company Join a global leader in healthcare technology, where innovation, safety, and user experience come together to improve patient outcomes. Within a highly regulated medical device environment, you will contribute to the development of safe, intuitive, and user-centered products used by healthcare professionals and patients worldwide. Role Description As a Usability Engineer & Validation Lead, you will be responsible for integrating human factors engineering and usability principles throughout the medical device development lifecycle. You will lead usability activities from early user research and requirements definition through design validation and post-market evaluation, ensuring products meet regulatory expectations, customer needs, and safety standards. Working closely with multidisciplinary global teams, you will influence product design decisions and ensure usability, quality, and patient safety are embedded into every stage of development. Key Responsibilities Lead usability engineering activities throughout the complete product development lifecycle Perform workflow analysis, user research, task analysis, and context-of-use evaluations to define user needs and usability requirements Develop usability engineering plans and coordinate activities with project managers, clinical marketing, engineering, and other stakeholders Lead usability risk management activities, including Usability FMEA Plan, execute, and document usability evaluations and ensure critical findings are incorporated into product improvements Analyze post-market data to identify usability issues and improvement opportunities Provide usability guidance to design teams regarding UI/UX solutions and design changes Ensure compliance with usability engineering standards, including IEC 62366-1, FDA Human Factors Guidance, and applicable global regulations Define product validation strategies, create validation plans and protocols, and execute design validation activities Develop high-quality technical documentation to support regulatory submissions and product releases Collaborate with multidisciplinary international teams across engineering, quality, regulatory, and product development Requirements Master's degree or PhD in Human Factors Engineering, Human-Computer Interaction (HCI), Cognitive Science, Product Design, Interaction Design, or a related field Minimum 2–3 years of experience in usability engineering within medical devices Proven experience across the full usability lifecycle, from user needs gathering through usability validation and post-market follow-up Experience performing task analysis, usability evaluations, and usability validation studies Experience supporting Design Validation, including validation strategies, protocols, execution, and reporting Strong understanding of medical device regulations and standards, including: IEC 62366-1, FDA Human Factors Guidance, EU MDR, ISO 13485, ISO 14971, FDA 21 CFR 820.30,NMPA guidelines Strong knowledge of human factors engineering, interaction design, cognitive ergonomics, and usability methodologies Experience collaborating within multidisciplinary and international teams Strong project management, communication, and stakeholder management skills Ability to advocate for user needs and challenge design decisions when required Excellent written and verbal English communication skills

Company: A leading global organization dedicated to delivering high-quality pharmaceutical products worldwide. The company values innovation, collaboration, and a commitment to excellence in healthcare supply chain management. Job Description: We are seeking a proactive and detail-oriented Supply Chain Operations Coordinator to join our team. The role involves managing the end-to-end coordination of pharmaceutical shipments, ensuring smooth import and export processes, and supporting global distribution activities. Responsibilities: - Coordinate and process supply orders daily to ensure timely distribution of pharmaceutical products globally. - Handle import/export documentation and ensure compliance with international shipping regulations. - Book shipments, monitor logistics status, and proactively address any potential issues. - Resolve service and transportation-related problems efficiently. - Manage return processes and collaborate with third-party logistics providers and internal teams. - Develop strong relationships with internal and external customers, including affiliates and distributors. - Participate in cross-functional project teams to improve supply chain processes. - Continuously review and suggest improvements to Order-to-Cash policies and procedures. - Maintain updated knowledge of GMP/GDP standards and ensure training requirements are met. - Support disaster recovery planning alongside corporate teams. - Perform other duties as necessary to support supply chain operations. Requirements: - Bachelor’s or Master’s degree with at least 2 years of supply chain experience in a GMP/GDP-regulated environment. - Ability to handle multiple tasks and work effectively within an international team. - Strong computer skills, including experience with ERP systems. - Excellent communication skills in English, both spoken and written. - Customer-focused attitude and attention to detail. - Problem-solving skills and ability to prioritize effectively. Other Information: If you are interested and want to apply, please submit your application via the apply button below and contact me.  

Company A leading provider of pharmaceutical manufacturing services, dedicated to high-quality production within a regulated environment. The company values precision, compliance, and continuous improvement to ensure the best outcomes for patients globally. Job Description We are seeking a skilled Production Operator - Semi-Automated Lines to join our client's team in Breda. This role involves operating and maintaining semi-automated production lines to ensure efficient, compliant, and high-quality manufacturing. The ideal candidate will support ongoing production activities, troubleshoot issues, and contribute to process improvements in a GMP-regulated setting. Responsibilities - Operate and oversee semi-automated production lines in line with SOPs and GMP standards. - Perform machine set-ups, changeovers, and line preparations. - Troubleshoot and resolve process disturbances to ensure smooth production flow. - Conduct minor mechanical and parameter adjustments to optimize equipment performance. - Record, verify, and document production data accurately in SAP/MES systems. - Ensure all GMP documentation, including batch records and logs, is completed correctly and on time. - Report deviations, participate in troubleshooting meetings, and support resolution efforts. - Execute daily, weekly, and monthly cleaning operations. - Support continuous improvement initiatives using Lean, Six Sigma, and other problem-solving methodologies. - Facilitate effective shift handovers and maintain clear communication within the team. - Uphold a safe, compliant, and well-organized working environment. Requirements - Minimum of 3 years’ experience in a production role, preferably in assembly and packaging. - Hands-on experience with automated and semi-automated production environments. - Fluent in English. - Comfortable working within structured procedures in a regulated GMP setting. - Willing to commute to Breda. - Able to work in shift systems. Other Information If you are interested and want to apply, please submit your application via the apply button below and contact me.  

  About Our Client Our client is one of the world's leading biotechnology companies, dedicated to developing innovative medicines that improve the lives of patients worldwide. Their international supply chain organization plays a vital role in ensuring these medicines reach healthcare providers and patients safely, efficiently, and on time. Working in a highly regulated GMP/GDP environment, you'll join a collaborative team that values quality, continuous improvement, and operational excellence. About the Position As an Associate Supply Chain (Import/Export), you will be responsible for coordinating the international movement of pharmaceutical products from manufacturing sites to customers around the globe. You'll oversee the complete order-to-delivery process, working closely with logistics providers, manufacturing sites, distributors, and internal stakeholders to ensure shipments are delivered accurately and on schedule. This role combines supply chain coordination, customer service, and international logistics in a fast-paced global environment. Key Responsibilities Coordinate international import and export shipments from order through delivery Process daily supply orders and ensure accurate execution Prepare and manage shipping and export documentation Monitor shipments proactively and resolve transportation or service issues Coordinate product returns and support exception handling Collaborate with logistics providers, manufacturing sites, affiliates, and distributors worldwide Build strong relationships with internal and external stakeholders Support cross-functional projects and continuous improvement initiatives Contribute to KPI reporting and process optimization Ensure all activities comply with GMP, GDP, and company quality standards Requirements Bachelor's degree with at least 2 years of supply chain experience, or a Master's degree Experience within a GMP and/or GDP regulated industry is preferred Knowledge of international logistics, import/export processes, or order management Experience with ERP systems and supply chain software is an advantage Strong organizational skills with the ability to manage multiple priorities simultaneously Customer-focused mindset with excellent communication skills Strong problem-solving abilities and attention to detail Comfortable working in an international and cross-functional environment Fluent in English, both written and spoken Motivated to drive process improvements and contribute to operational excellence

The Company A global pharmaceutical and biotechnology organization focused on developing innovative therapies and improving patient outcomes worldwide. The company operates within a highly regulated environment and manages complex international supply chain and warehouse networks to ensure product availability across global markets. Role description We are looking for a Senior Associate Supply Chain to support global warehouse analytics and capacity planning activities. This position focuses on developing standardized dashboards, performing warehouse capacity analysis, and delivering actionable insights across multiple international warehouse locations. The role combines supply chain knowledge, data analytics, stakeholder engagement, and reporting expertise to support warehouse planning, governance activities, and operational decision making. Responsibilities - Build, maintain, and improve warehouse capacity dashboards and automated reporting - Standardize reporting and analytics across global warehouse sites - Perform recurring warehouse capacity analysis and scenario assessments - Monitor warehouse utilization, constraints, and emerging capacity risks - Validate warehouse master data including storage types, pallet information, and capacity constraints - Support planning cycles and governance forums through reporting and analytical insights - Identify data quality issues and collaborate with stakeholders to resolve them - Coordinate with planning teams, warehouse experts, and system owners to ensure accurate data inputs - Translate business requirements into analytics deliverables and reporting solutions - Drive continuous improvement initiatives and identify operational efficiencies Requirements - Bachelor degree in Supply Chain, Logistics, Business Administration, or related field - Experience with Power BI and/or Databricks - Strong data analytics and dashboard development experience - Understanding of supply chain planning processes - SAP experience including inventory management, capacity planning, or Plan to Stock processes - Advanced Microsoft Office skills, particularly Excel - Strong analytical and problem solving abilities - Excellent communication and stakeholder management skills - Fluent English communication skills - Ability to work independently and proactively - Experience within warehouse, logistics, or supply chain operations Other Information - Hybrid working model

Company Our client is a large industrial manufacturing organisation with a strong focus on safety, operational excellence, and sustainability. The site operates in a complex, high-compliance environment where reliability and continuous improvement are critical to performance. Job Description For our client in Dordrecht, we are looking for a Senior Maintenance & Reliability Team Lead (Asset Care). In this role, the Senior Maintenance & Reliability Team Lead (Asset Care) drives the site’s asset care and maintenance excellence agenda, improving equipment reliability and performance while leading a multidisciplinary engineering team. The position works closely with stakeholders across the plant to ensure corrective maintenance escalations are handled effectively and long-term reliability improvements are delivered. Responsibilities - Lead and develop a team of maintenance and reliability professionals, including engineering and turnaround coordination. - Design, implement, monitor, and continuously improve the Asset Care / Maintenance Excellence programme aligned to site targets (e.g., OEE, efficiency, and process safety objectives). - Manage and prioritise daily escalations related to corrective maintenance to reduce downtime and operational risk. - Track, analyse, and report performance through relevant KPIs; communicate progress, risks, and priorities to key stakeholders. - Drive root-cause problem solving and structured improvement using recognised reliability methodologies. - Align local execution with broader (site or global) standards and ways of working, supporting change initiatives across people and assets. Requirements - Bachelor’s or Master’s degree (or equivalent experience). - 10+ years of experience in Maintenance, Reliability, and/or Turnarounds within an industrial environment. - Proven people leadership and change management experience (leading teams of 5+ and driving operational change). - Solid knowledge of reliability and problem-solving methods such as RCFA, FMEA, 5-Why, condition-based monitoring, and NDT concepts. - Good understanding of Maintenance Excellence principles (e.g., TPM). - Strong stakeholder management and communication skills. - Fluent in Dutch and English. - Temporary Full Time Contract via SIRE   Other Information If you are interested and want to apply, please submit your application via the apply button below and contact me.