Customer Operations Coordinator, Meppel, Drenthe

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.

Company A leading organization committed to advancing supply chain efficiency and digital innovation within the pharmaceutical industry. The company emphasizes operational excellence, collaboration, and continuous improvement to support its global health initiatives. Job Description We are seeking a knowledgeable and proactive Supply Chain Digital Transformation Specialist to join our team. In this role, you will support global supply chain digital projects, optimise processes, and act as a key liaison for systems and operational improvements within the OTC and PTS areas. Responsibilities -Provide daily operational support for ERP systems, ensuring smooth execution of OTC and PTS processes, including access management, troubleshooting, and training -Assist in the implementation of global digital supply chain initiatives, such as ERP and EDI systems -Maintain and update master data in ERP systems for sales views and product launches -Track and report on the progress of global supply chain projects and initiatives -Lead or contribute to process improvement projects, gathering business -requirements, conducting user acceptance tests, and documenting changes -Manage minor system enhancements and updates to departmental SOPs, work instructions, and training materials -Act as a subject matter expert for PTS and OTC processes, representing the -global supply chain in cross-functional teams including compliance and quality groups -Support the development of business cases and project charters for ERP system improvements -Facilitate continuous process improvements and participate in multiple initiatives to optimise supply chain performance Requirements -Bachelor’s degree in logistics, economics, information technology or related fields -Minimum of 3 years' experience in international supply chain management, preferably in the pharmaceutical industry -Proficiency in MS Office and ERP systems, preferably SAP (especially OTC and PTS modules) -Strong understanding of end-to-end supply chain processes, digital supply chain tools, and EDI communication methods -Experience managing cross-cultural teams and working across different geographies -Proven project management skills and business ownership experience -Excellent analytical, communication, and presentation skills -Fluent in English, both written and spoken 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 Join a global biotechnology company dedicated to improving patients’ lives through innovative medicines. The Breda site is a highly automated, GMP-regulated manufacturing facility supplying medicines to more than 75 countries worldwide. Role Overview As a Technical Operator, you will operate and monitor automated production equipment, troubleshoot technical issues and ensure safe, efficient and compliant manufacturing within a GMP environment. Key Responsibilities -  Operate automated manufacturing, assembly, labelling and packaging equipment. -  Perform equipment setup, changeovers, cleaning and line clearance. -  Follow GMP standards, SOPs and safety procedures. -  Record production data using SAP/MES and maintain accurate batch documentation. -  Troubleshoot equipment issues and support deviations and root cause analysis. -  Perform routine inspections, equipment adjustments and basic first-line maintenance. -  Contribute to Lean Manufacturing and continuous improvement initiatives. -  Collaborate with Production, Engineering, Maintenance and Quality teams. Requirements -  MBO-level technical qualification or equivalent experience. -  Hands-on experience in manufacturing or production, preferably with automated machinery. -  Experience in pharmaceutical, biotechnology or another quality-controlled environment is an advantage. -  Knowledge of GMP, SOPs, SAP/MES and structured troubleshooting. -  Strong problem-solving skills, attention to detail and a quality-focused mindset. -  Good English communication skills. -  Willingness to commute to Breda and work rotating 3-shift or 5-shift schedules. Other Information Opportunity to work in a highly automated pharmaceutical manufacturing environment. Competitive compensation and shift-related benefits. Technical development and career progression opportunities. A collaborative workplace focused on quality and continuous improvement. Interested? Contact me to learn more about the role, shift schedule and compensation pack  

The Company A global pharmaceutical manufacturing organization focused on producing high quality medicines and healthcare products. The company operates in highly regulated production environments with a strong emphasis on safety, operational excellence, quality compliance, and continuous employee development About the Role We are seeking motivated Production Operators to support manufacturing activities in a regulated pharmaceutical production environment. This position is ideal for candidates looking to build a strong foundation in GMP manufacturing while gaining hands on experience with production processes, equipment operation, and quality systems. Responsibilities - Execute production activities according to approved procedures, GMP requirements, and safety standards - Prepare production materials, equipment, and work areas for operational activities - Operate production equipment following training and approved instructions - Complete accurate and timely documentation of all assigned activities - Follow GMP guidelines and quality requirements at all times - Identify deviations, abnormalities, and safety concerns and escalate appropriately - Support smooth shift handovers and maintain effective communication within the team - Participate in training programs and on the job learning activities - Contribute to maintaining a safe, clean, and compliant production environment - Collaborate with operators and production colleagues to ensure operational continuity Requirements - MBO level education, preferably in a technical, manufacturing, engineering, pharmaceutical, biotechnology, or life sciences discipline - Fluent Dutch and English language skills, both written and verbal - Ability to work in a structured and regulated manufacturing environment - Strong attention to detail and commitment to quality - Understanding of GMP principles is advantageous - Willingness to work in rotating shift patterns - Strong team player with good communication skills - Reliable, accurate, and safety conscious work approach - Ability to learn new processes and technologies quickly - Flexible and adaptable mindset - Comfortable following standard operating procedures - Eligible to complete PESV screening Other Information If you are interested and want to apply, please submit your application via the apply button below and contact me.

The Company Our client is one of the leads from the Biotechnology industry who try to improve patients’ lives, by distributing their medicines to hospital and pharmacies in 100 different countries in the world, to over 10 million patients, in Europe, Turkey, Middle East and Africa Regions. Job Description As a Utilities Maintenance Supervisor, you will oversee the maintenance and reliable operation of critical utility systems, including HVAC, refrigeration, chillers, compressed air, and boilers. You will coordinate and support a team of technicians, troubleshoot technical issues, and drive continuous improvements while ensuring safe and efficient operations in a regulated manufacturing environment. Key Responsibilities Planning, coordinating, and prioritizing maintenance activities for utility systems and building infrastructure. Providing technical guidance, coaching, and support to technicians and contractors. Troubleshooting complex issues related to utility systems and collaborating with engineering teams to find effective solutions. Working closely with contractors, vendors, and internal teams to resolve technical challenges and optimize system performance. Leading initiatives to improve system reliability and drive continuous improvement projects. Participating in an on-call rotation to support critical utility systems outside regular working hours. Requirements MBO+/HBO-level education or equivalent technical experience. Experience in utilities, facilities maintenance, or industrial installations. Strong troubleshooting skills with a hands-on approach. Proven ability to coordinate maintenance projects, manage contractors, and lead technical teams. Excellent communication skills in English and a collaborative attitude. Willingness to participate in an on-call support rotation. Previous experience in a GMP environment and familiarity with SAP PM or similar CMMS systems are advantageous. Other Information Apply to our vacancy for more information. We look forward to hearing from you!

Company: A leading biotechnology organization dedicated to serving patients worldwide. This company provides innovative medicines across a global network, focusing on maintaining a strong scientific foundation while fostering an entrepreneurial spirit. They promote fulfilling careers through challenging projects, professional development, and meaningful opportunities within a diverse and dynamic environment. Job Description: We are seeking a detail-oriented Senior Quality Assurance Specialist to oversee QA activities within the clinical supply chain. The role involves ensuring compliance with GMP and GDP standards for clinical trial products, supporting manufacturing and distribution processes, and maintaining high-quality standards across all supply chain operations. Responsibilities: •    Provide QA oversight for the clinical supply chain, including receipt, storage, and distribution of clinical trial products. •    Review and support batch certification processes to ensure compliance with EU and international regulations. •    Approve clinical label artwork and review deviations, ensuring procedural adherence. •    Assess and manage temperature excursions during transport and at clinical sites. •    Collaborate with stakeholders such as Global Clinical Supply Chain, Warehouse, Production, Quality, Clinical Research, and Regulatory Affairs to resolve compliance issues. •    Develop, review, and update SOPs and work instructions to align with corporate and regulatory standards. •    Prepare and analyze monthly quality metrics. •    Support on-site clinical packaging and labeling operations — including batch record review and issue resolution. •    Identify quality issues and work cross-functionally to implement corrective actions. Requirements: •    Master’s degree in Life Sciences or a related field. •    At least 3 years of QA or manufacturing experience within the pharmaceutical or medical device industry. •    Knowledge of GMP, GDP, and GCP regulations. •    Fluent in English, with strong communication skills. Other Information: If you are interested and want to apply, please submit your application via the apply button below and contact me.

Company A highly automated, fast-growing manufacturing site is expanding its operations and investing heavily in modern facilities, automation, and infrastructure. The environment is international, safety-driven, and strongly focused on quality and compliance. The site relies on critical utility systems to keep production, warehousing, and office operations running reliably every day. Job Description The Utilities Maintenance Team Lead supports the reliable operation of essential utility and facility systems in a complex industrial environment. This role combines strong hands-on technical knowledge with day-to-day coordination and coaching of technicians and external contractors. The Utilities Maintenance Team Lead helps ensure maintenance work is planned and executed safely, efficiently, and in line with compliance expectations, while also contributing to continuous improvement and reliability initiatives. Responsibilities - Coordinate, plan, and prioritize preventive and corrective maintenance across utility and facility systems. - Provide technical guidance, coaching, and practical support to technicians and contractors. - Troubleshoot and support resolution of complex issues related to utilities and building infrastructure. - Work closely with engineering, operations, and external vendors to align on technical solutions and execution plans. - Support reliability improvements and continuous improvement initiatives to reduce downtime and improve system performance. - Ensure maintenance activities are performed with a strong focus on safety, quality, and compliant documentation. - Participate in an on-call rotation to support critical systems when needed. Requirements - Relevant technical education or equivalent practical experience. - Experience with utilities, facilities, maintenance, or industrial installations. - Strong troubleshooting skills and a hands-on mindset. - Experience coordinating maintenance work, contractors, projects, or technical teams. - Strong communication skills and the ability to coach and support others. - Good English communication skills. - Experience in a regulated environment and familiarity with maintenance management systems (e.g., SAP PM or similar) is a plus. Other Information This is an opportunity for a professional who enjoys being close to the operation and wants to take ownership of critical infrastructure that directly supports site performance and growth. 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 globally operating biotechnology organization dedicated to developing and delivering high-quality medicines to patients worldwide. The site in Breda, the Netherlands, plays an important role in pharmaceutical manufacturing and packaging operations, maintaining high standards of quality, safety, and regulatory compliance. Job Description For our client in Breda, we are looking for a Manufacturing Technician to support pharmaceutical manufacturing activities. In this role, you will be responsible for running automated production equipment, maintaining efficient manufacturing processes, resolving technical issues, and ensuring all activities comply with Good Manufacturing Practices (GMP). Responsibilities - Run, control, and supervise automated production machinery and manufacturing lines. - Configure, set up, and adjust equipment according to production requirements. - Detect, diagnose, and resolve machine faults, process interruptions, and technical issues. - Enhance equipment performance and improve production efficiency. - Follow GMP regulations, Standard Operating Procedures (SOPs), work instructions, and safety guidelines. - Complete, update, and verify batch records, production logs, and manufacturing documentation. - Enter and validate production data using systems such as SAP and MES. - Report, document, and support investigations into deviations and abnormal process conditions. - Collaborate with Quality Assurance, Maintenance, Engineering, and Production teams to resolve operational problems. - Prepare, clean, and restore equipment during production changeovers and shutdowns. - Contribute to root cause analysis, Lean manufacturing, and continuous improvement initiatives. -Ensure the production area and equipment meet pharmaceutical quality and cleanliness standards. Requirements - Previous experience in manufacturing, machine operation, production, or process operations. - Experience working with automated machinery or industrial production lines is an advantage. - Technical knowledge of machine settings, equipment adjustments, and fault diagnosis. - Understanding of GMP, SOPs, batch records, and production documentation is desirable. - Experience with SAP, MES, or other manufacturing systems is a plus. - A background in mechanical engineering, mechatronics, electrical engineering, or a related technical field is beneficial. - Strong problem-solving skills, attention to detail, and a quality-focused mindset. - Ability to work collaboratively with cross-functional teams. - Willingness to work in a shift-based environment. Other Information The role is based on-site in Breda, the Netherlands, and offers the opportunity to work in a regulated pharmaceutical manufacturing environment with modern automated production equipment. If you are interested in this opportunity and would like to apply, please submit your application via the apply button below or contact me for more information.