Farmacie & Geneesmiddelen Vacatures in Sint Annaland

Over de vacature

Please note before applying: We can only consider candidates who are already settled in the Netherlands. This position does not offer sponsorship. Applicants must have a valid work permit for the Netherlands.
As a Supply Chain Project Manager, you will play a key role in the successful launch and lifecycle management of pharmaceutical products. You will coordinate supply chain activities across different departments, ensure projects stay on track, and make sure product launches and changes are implemented on time and in line with quality requirements.You will translate product launch and lifecycle strategies into clear supply chain plans and coordinate their execution from start to finish. A major part of the role is managing change controls, tracking project milestones, and bringing together stakeholders from different functions to ensure smooth implementation.
Key Responsibilities - Lead and coordinate end-to-end supply chain projects related to new product launches, product changes, and lifecycle management.

• Own and maintain the overall project plan , ensuring activities, deadlines, and milestones are clearly defined and followed.
• Manage Change Controls and make sure they are implemented correctly, on time, and in line with company procedures.
• Organize and facilitate Product Lifecycle Team and Project Management meetings.
• Coordinate closely with departments such as Quality Assurance, Regulatory Affairs, Production, Planning, Artwork, Warehouse, Customer Service, and Procurement.
• Support the implementation of new products, product variations, packaging changes, and other lifecycle activities.
• Prepare project updates, reports, and key performance metrics for internal stakeholders and management.
• Support the development of project plans, project charters, workshops, and business cases.
• Identify potential issues and opportunities for improvement and lead projects to make processes more efficient.
• Act as a central point of contact to ensure all relevant stakeholders are aligned and that projects progress smoothly.

Requirements

• Bachelor’s degree or equivalent with typically 3–5+ years of relevant professional experience , or
• Master’s degree or equivalent with typically 1–3+ years of relevant professional experience , or
• PhD or equivalent with relevant professional experience.
• Previous experience in Project Management , ideally in a complex, cross-functional environment.
• Strong analytical and problem-solving skills with the ability to identify issues and develop practical solutions.
• Excellent communication and stakeholder management skills .
• Strong organizational skills and the ability to manage multiple projects, priorities, and deadlines simultaneously.
• A proactive and collaborative approach to working with different departments and stakeholders.
• Experience in the pharmaceutical industry is preferred.
• Knowledge of Supply Chain, product launches, change management, or lifecycle management is an advantage.

Benefits

• Full-time position.
• Competitive salary package.
• 30 Holidays.
• Travel reimbursement, dependent on distance.
• Hybrid position plus working from home allowance.
• 1 year Contract via Undutchables with long-term growth opportunities in a dynamic, international setting.

Application Procedure

If you are interested in this vacancy, you can apply by clicking on the button above. By clicking on apply, you agree to our privacy commitment and terms and conditions . Your application will be sent directly to the recruiter in charge. IMPORTANT: if you are not yet registered with Undutchables we kindly ask you to do so. Your information will be handled in the strictest confidence and your CV will not be sent to a company unless you have given prior permission. Curious about how the recruitment process works within Undutchables, click here to read more.

Over de vacature

You will take ownership of the mid- and long-term supply plan for your assigned products and production lines. A major part of your role will be preparing and managing the *rough-cut capacity plan for a planning horizon of approximately 4 to 24 months

• , with particular attention to the 4–5 month horizon where plans become increasingly operational. You will work in an environment where production capacity is limited, meaning that careful prioritization and strategic decision-making are essential. You will continuously balance demand, available capacity, inventory levels, product life cycles, and supply risks to maintain a stable and reliable supply.Your responsibilities will include:

• Developing and managing tactical and strategic supply plans for assigned products and production lines.
• Preparing and maintaining rough-cut capacity plans for the mid- and long-term planning horizon.
• Managing supply planning, capacity planning, inventory levels, routings, OAE, and MPS.
• Proactively assessing inventory positions and ensuring alignment with strategic inventory targets.
• Identifying capacity constraints, supply risks, and potential stock issues and developing appropriate solutions.
• Working towards a stable and efficient supply plan and investigating deviations through root-cause analysis and corrective actions.
• Performing scenario analyses to support strategic supply chain decisions.
• Supporting product launches, phase-outs, life cycle management, and variation management.
• Considering production capacity utilization, component availability, costs, cash impact, and potential scrap when making planning decisions.
• Working strategically with global suppliers regarding drug products and drug substance to optimize shelf life and minimize scrap.
• Ensuring planning cycles are completed accurately and on time.
• Collaborating closely with production and supply sites to ensure a seamless flow of supply.
• Communicating with critical resource owners and other key stakeholders across the organization.
• Participating in weekly and monthly tactical and strategic planning meetings.
• Collaborating with international and global teams and providing input and advice on strategic decisions.
• Identifying opportunities for process and supply chain improvements.
• Following established policies and procedures associated with the role.

*Candidates must hold a valid work permit for the Netherlands and live within reasonable commuting distance from Breda. Applications from candidates who do not meet this criteria will be declined immediately.

Requirements

• A Master's degree in Supply Chain, Business Administration, Engineering, or a related field.
• At least *7 years of relevant experience in rough-cut capacity planning

• within a supply chain environment.

• Strong experience with supply planning and capacity planning.
• Experience with routings, OAE, and MPS.
• Strong knowledge of inventory management.
• Experience working with complex data in a capacity-constrained environment.
• Experience with process and continuous improvement.
• Experience working in an international environment.
• Strong analytical and problem-solving skills.
• Excellent stakeholder management and communication skills.
• An end-to-end supply chain mindset.
• A proactive attitude and strong sense of ownership.
• The ability to move easily between strategic discussions and more technical planning topics.
• A can-do mentality and the drive to take responsibilities through to completion.

Strongly preferred - Experience within the pharmaceutical industry.

• Knowledge of pharmaceutical life cycle management and variation management.
• Understanding of working within a GDP/regulatory environment.
• Experience with SAP.
• Experience with Rapid Response.
• Knowledge of Lean, Six Sigma, or other Continuous Improvement methodologies and tools.

Benefits

• *Contract duration:

• 1 year via undutchables

• *Hours:

• Full-time

• *Working model:

• Hybrid, with approximately 2–3 days per week on-site

• *Location:

• Breda

Application Procedure

If you are interested in this vacancy, you can apply by clicking on the button above. By clicking on apply, you agree to our privacy commitment and terms and conditions . Your application will be sent directly to the recruiter in charge. IMPORTANT: if you are not yet registered with Undutchables we kindly ask you to do so. Your information will be handled in the strictest confidence and your CV will not be sent to a company unless you have given prior permission. Curious about how the recruitment process works within Undutchables, click here to read more.

Over de vacature

As Senior Associate Contracts & Pricing, you will act as an important link between different departments and international affiliates. When local teams negotiate contracts and prices, you help make sure these agreements are correctly translated into systems and processes. This is *not a role in which you will draft or negotiate contracts yourself

• . Instead, you will be the operational expert and advisor who makes sure contracts and pricing processes are followed correctly and lead to the expected results in areas such as orders, payments and revenue recognition. Your responsibilities will include:

• Acting as a main point of contact for international affiliates regarding contracts and pricing processes;
• Supporting colleagues with operational questions, issues and requests and helping them find the right solution;
• Making sure contract and pricing information is correctly processed and set up in the relevant systems;
• Working closely with departments such as Finance, Accounting, Commercial, Supply Chain and Operations;
• Supporting governance and ensuring procedures, documentation and controls are followed correctly;
• Helping maintain accurate and audit-ready processes;
• Analysing processes and identifying opportunities to improve efficiency, consistency and compliance;
• Supporting process changes, system improvements and international projects;
• Creating and maintaining process documentation, procedures, training materials and Quick Reference Guides;
• Providing training and guidance to business users;
• Analysing operational data and using your findings to support business decisions;
• Sharing best practices across countries and teams.

You will work extensively with *SAP and Vistex

• , a solution integrated with SAP that supports pricing and contract-related processes. Previous Vistex experience is not required, but you should be comfortable working with business systems and able to learn new tools quickly. #

Requirements

For this position, we are looking for someone who enjoys working in a structured international organization and is comfortable taking responsibility for their own work. You learn quickly, ask the right questions and don't simply work based on assumptions.You bring: - A Bachelor's/Master's degree with at least 2 years of relevant professional experience, or an Associate's degree with at least 5 years of relevant experience;

• Experience within a corporate, preferably multinational, organization;
• Relevant experience within areas such as contracts & pricing, finance, business administration, commercial operations or Order to Cash;
• Experience working with multiple stakeholders across departments such as Finance, Commercial, Supply Chain and Operations;
• Good understanding of business processes and preferably financial/accounting processes;
• Experience with SAP is strongly preferred;
• Strong Excel and PowerPoint skills and experience working with reporting tools;
• Fluent English communication skills.
• Experience within the *pharmaceutical or biotechnology industry

• is an advantage. Experience from another highly structured and regulated environment, such as medical devices or food, can also be relevant.

• Experience with *Vistex and/or Tableau

• is considered a plus, but is not required.

Benefits

• This is a *full-time position for 40 hours per week

• , initially for approximately one year via Undutchables. Depending on future business needs, there may be a possibility of extension.

• The standard working model is hybrid, with *Tuesday and Thursday as office days in Breda

• . During the first months, training and work-shadowing period, however, you should be prepared to work from the Breda office more frequently.

• Ideally, you are available to start around *mid-November or early December 2026

• .

• Travel reimbursement
• 30 Holidays
• Pension scheme

Application Procedure

If you are interested in this vacancy, you can apply by clicking on the button above. By clicking on apply, you agree to our privacy commitment and terms and conditions . Your application will be sent directly to the recruiter in charge. IMPORTANT: if you are not yet registered with Undutchables we kindly ask you to do so. Your information will be handled in the strictest confidence and your CV will not be sent to a company unless you have given prior permission. Curious about how the recruitment process works within Undutchables, click here to read more.

Over de vacature

This role is crucial for ensuring the quality and compliance of essential product documentation and master data. As a Quality Assurance Associate, you will play a vital part in safeguarding product integrity by meticulously reviewing and approving critical information. The ideal candidate will thrive in an environment that demands precision and a strong compliance mindset, contributing directly to the company's commitment to excellence.Your key responsibilities will include:

• Performing detailed quality reviews and approvals of artworks for various products.
• Conducting thorough quality checks and approvals for Bill of Materials (BOMs).
• Reviewing and approving critical fields within the master data system to ensure accuracy and compliance.
• Executing precise checks and verifying information against established procedures and regulatory standards.
• Collaborating effectively with team members to manage workload distribution and ensure timely completion of tasks.
• Identifying potential issues or discrepancies and proactively following up to ensure their resolution.
• Adhering strictly to Good Manufacturing Practice (GMP) guidelines and internal quality procedures.

Please note that we are unable to consider candidates who require visa sponsorship or who live too far from the work location. Candidates who would need to relocate can only be considered if they have already secured accommodation within a reasonable commuting distance. #

Requirements

We are looking for a highly detail-oriented and compliance-minded individual who is eager to contribute to a rigorous quality assurance process. You should possess a strong sense of responsibility, excellent communication skills, and a collaborative spirit to work effectively within a diverse team. The ideal candidate is proactive in identifying issues and committed to understanding the importance of accurate checks in a regulated environment. Character and mindset are paramount for success in this role. - English – C1 (spoken and written)

• Relevant educational background (e.g., Bachelor's or Master's degree in a scientific field)
• Some relevant in a regulated industry (e.g., Pharma, Food) is highly preferred
• Ability to perform highly detailed and precise review tasks
• Strong collaborative and communication skills
• Proficiency in standard office software; familiarity with SAP is a plus but not required

Benefits

• This is a 6-month contract position through Undutchables, with the possibility of future opportunities within the company, though no guarantees can be made for an extension in this specific role.
• Working hours: Full-time (40 hours/week) is preferred, but 32 hours/week is also an option.
• Hybrid work model: During the initial training period (approx. 1.5 months), you will be expected to be on-site 3-4 days per week. After training, a minimum of 2 days per week on-site is required, with Thursdays being a fixed office day.
• Competitive salary package.
• Pension scheme
• Travel expense reimbursement, dependent on distance.
• Dynamic, international, and collaborative work environment with excellent development opportunities.

Application Procedure

If you are interested in this vacancy, you can apply by clicking on the button above. By clicking on apply, you agree to our privacy commitment and terms and conditions . Your application will be sent directly to the recruiter in charge. IMPORTANT: if you are not yet registered with Undutchables we kindly ask you to do so. Your information will be handled in the strictest confidence and your CV will not be sent to a company unless you have given prior permission. Curious about how the recruitment process works within Undutchables, click here to read more.

Over de vacature

Please note before applying: We can only consider candidates who are already settled in the Netherlands. This position does not offer sponsorship. Applicants must have a valid work permit for the Netherlands.
As a Supply Chain Project Manager, you will play a key role in the successful launch and lifecycle management of pharmaceutical products. You will coordinate supply chain activities across different departments, ensure projects stay on track, and make sure product launches and changes are implemented on time and in line with quality requirements.You will translate product launch and lifecycle strategies into clear supply chain plans and coordinate their execution from start to finish. A major part of the role is managing change controls, tracking project milestones, and bringing together stakeholders from different functions to ensure smooth implementation.
Key Responsibilities - Lead and coordinate end-to-end supply chain projects related to new product launches, product changes, and lifecycle management.

• Own and maintain the overall project plan , ensuring activities, deadlines, and milestones are clearly defined and followed.
• Manage Change Controls and make sure they are implemented correctly, on time, and in line with company procedures.
• Organize and facilitate Product Lifecycle Team and Project Management meetings.
• Coordinate closely with departments such as Quality Assurance, Regulatory Affairs, Production, Planning, Artwork, Warehouse, Customer Service, and Procurement.
• Support the implementation of new products, product variations, packaging changes, and other lifecycle activities.
• Prepare project updates, reports, and key performance metrics for internal stakeholders and management.
• Support the development of project plans, project charters, workshops, and business cases.
• Identify potential issues and opportunities for improvement and lead projects to make processes more efficient.
• Act as a central point of contact to ensure all relevant stakeholders are aligned and that projects progress smoothly.

Requirements

• Bachelor’s degree or equivalent with typically 3–5+ years of relevant professional experience , or
• Master’s degree or equivalent with typically 1–3+ years of relevant professional experience , or
• PhD or equivalent with relevant professional experience.
• Previous experience in Project Management , ideally in a complex, cross-functional environment.
• Strong analytical and problem-solving skills with the ability to identify issues and develop practical solutions.
• Excellent communication and stakeholder management skills .
• Strong organizational skills and the ability to manage multiple projects, priorities, and deadlines simultaneously.
• A proactive and collaborative approach to working with different departments and stakeholders.
• Experience in the pharmaceutical industry is preferred.
• Knowledge of Supply Chain, product launches, change management, or lifecycle management is an advantage.

Benefits

• Full-time position.
• Competitive salary package.
• 30 Holidays.
• Travel reimbursement, dependent on distance.
• Hybrid position plus working from home allowance.
• 1 year Contract via Undutchables with long-term growth opportunities in a dynamic, international setting.

Application Procedure

If you are interested in this vacancy, you can apply by clicking on the button above. By clicking on apply, you agree to our privacy commitment and terms and conditions . Your application will be sent directly to the recruiter in charge. IMPORTANT: if you are not yet registered with Undutchables we kindly ask you to do so. Your information will be handled in the strictest confidence and your CV will not be sent to a company unless you have given prior permission. Curious about how the recruitment process works within Undutchables, click here to read more.

Over de vacature

You will take ownership of the mid- and long-term supply plan for your assigned products and production lines. A major part of your role will be preparing and managing the *rough-cut capacity plan for a planning horizon of approximately 4 to 24 months

• , with particular attention to the 4–5 month horizon where plans become increasingly operational. You will work in an environment where production capacity is limited, meaning that careful prioritization and strategic decision-making are essential. You will continuously balance demand, available capacity, inventory levels, product life cycles, and supply risks to maintain a stable and reliable supply.Your responsibilities will include:

• Developing and managing tactical and strategic supply plans for assigned products and production lines.
• Preparing and maintaining rough-cut capacity plans for the mid- and long-term planning horizon.
• Managing supply planning, capacity planning, inventory levels, routings, OAE, and MPS.
• Proactively assessing inventory positions and ensuring alignment with strategic inventory targets.
• Identifying capacity constraints, supply risks, and potential stock issues and developing appropriate solutions.
• Working towards a stable and efficient supply plan and investigating deviations through root-cause analysis and corrective actions.
• Performing scenario analyses to support strategic supply chain decisions.
• Supporting product launches, phase-outs, life cycle management, and variation management.
• Considering production capacity utilization, component availability, costs, cash impact, and potential scrap when making planning decisions.
• Working strategically with global suppliers regarding drug products and drug substance to optimize shelf life and minimize scrap.
• Ensuring planning cycles are completed accurately and on time.
• Collaborating closely with production and supply sites to ensure a seamless flow of supply.
• Communicating with critical resource owners and other key stakeholders across the organization.
• Participating in weekly and monthly tactical and strategic planning meetings.
• Collaborating with international and global teams and providing input and advice on strategic decisions.
• Identifying opportunities for process and supply chain improvements.
• Following established policies and procedures associated with the role.

*Candidates must hold a valid work permit for the Netherlands and live within reasonable commuting distance from Breda. Applications from candidates who do not meet this criteria will be declined immediately.

Requirements

• A Master's degree in Supply Chain, Business Administration, Engineering, or a related field.
• At least *7 years of relevant experience in rough-cut capacity planning

• within a supply chain environment.

• Strong experience with supply planning and capacity planning.
• Experience with routings, OAE, and MPS.
• Strong knowledge of inventory management.
• Experience working with complex data in a capacity-constrained environment.
• Experience with process and continuous improvement.
• Experience working in an international environment.
• Strong analytical and problem-solving skills.
• Excellent stakeholder management and communication skills.
• An end-to-end supply chain mindset.
• A proactive attitude and strong sense of ownership.
• The ability to move easily between strategic discussions and more technical planning topics.
• A can-do mentality and the drive to take responsibilities through to completion.

Strongly preferred - Experience within the pharmaceutical industry.

• Knowledge of pharmaceutical life cycle management and variation management.
• Understanding of working within a GDP/regulatory environment.
• Experience with SAP.
• Experience with Rapid Response.
• Knowledge of Lean, Six Sigma, or other Continuous Improvement methodologies and tools.

Benefits

• *Contract duration:

• 1 year via undutchables

• *Hours:

• Full-time

• *Working model:

• Hybrid, with approximately 2–3 days per week on-site

• *Location:

• Breda

Application Procedure

If you are interested in this vacancy, you can apply by clicking on the button above. By clicking on apply, you agree to our privacy commitment and terms and conditions . Your application will be sent directly to the recruiter in charge. IMPORTANT: if you are not yet registered with Undutchables we kindly ask you to do so. Your information will be handled in the strictest confidence and your CV will not be sent to a company unless you have given prior permission. Curious about how the recruitment process works within Undutchables, click here to read more.

Over de vacature

Our client is looking for a Senior Technical Project Manager to support the expansion and modernization of their manufacturing operations in Breda.In this role, you will lead multiple technical IT projects and workstreams, focusing on the implementation of new manufacturing technologies, automation systems, and digital solutions. Projects may include the deployment of new packaging lines, manufacturing system integrations, digital twin technology, smart vision systems, and other digital manufacturing innovations.You will work in a complex matrix organization, collaborating closely with Engineering, IT, Automation, Quality, Operations, external suppliers, and global technology teams. As the Project Manager, you will coordinate specialists from different departments and ensure projects are delivered successfully, from initial planning through implementation, validation, and operational handover.The position is primarily focused on project management rather than hands-on technical work . While an understanding of manufacturing technologies is important, you will be supported by technical specialists and global experts throughout the projects. Your main responsibilities will include:

• Lead complex technical IT and digital manufacturing projects from initiation through implementation and operational handover.
• Manage multiple projects and workstreams simultaneously, ensuring priorities, timelines, budgets, and deliverables remain on track.
• Develop and maintain detailed project plans, including milestones, resources, dependencies, risks, and key decisions.
• Coordinate the implementation and integration of manufacturing technologies, automation systems, digital solutions, and supporting infrastructure.
• Work closely with Engineering, Quality, Operations, IT/OT, Automation, and Validation teams to ensure successful project delivery.
• Manage relationships with internal stakeholders, external vendors, system integrators, and equipment suppliers.
• Coordinate technical requirements, design reviews, testing, qualification, validation, and system release activities.
• Identify potential risks, resolve challenges, and manage changing priorities within a complex manufacturing environment.
• Ensure projects comply with GMP, quality, cybersecurity, validation, and data integrity requirements.
• Support change management activities, including the introduction of new technologies, employee training, and operational readiness.
• Communicate project progress, challenges, and recommendations clearly to stakeholders at different organizational levels.
• Ensure appropriate documentation, support, ownership, and training are established before handing over completed projects to operational teams.

Requirements

To be successful in this role, you bring: - A Bachelor's or Master's degree in Engineering, Automation, Manufacturing Systems, Information Technology, Project Management, or a related field.

• Approximately 10–15 years of project management experience , preferably involving technical IT, manufacturing technology, automation, or digital transformation projects.
• Previous experience working within the pharmaceutical or biopharmaceutical industry, preferably in a large and complex manufacturing organization.
• Strong knowledge of GMP requirements and experience managing projects within a GMP-regulated environment.
• Experience managing complex technical projects from planning and design through implementation, validation, and operational handover.
• Experience working in a matrix organization, coordinating specialists and stakeholders from different departments.
• Strong project planning, risk management, problem-solving, and organizational skills.
• The ability to manage multiple projects and changing priorities while maintaining a clear overview.
• Excellent interpersonal and communication skills, with the ability to connect with people at different organizational levels.
• Professional fluency in English.

The following experience would be considered an advantage: - Knowledge of manufacturing systems, automation, SCADA, MES, IT/OT integration, digital manufacturing, or data platforms.

• Familiarity with technologies such as IIoT, Smart Vision, Digital Twin, or PlantPulse.
• Understanding of validation, commissioning, change control, and system lifecycle management.
• Project management certification such as PMP, PRINCE2, Agile, or equivalent.

Benefits

• This is a full-time position for 40 hours per week , initially for approximately one year via Undutchables, with the possibility for extension.
• The standard working model is hybrid, with three days per week in the office in Breda .
• Travel reimbursement
• 30 Holidays
• Pension scheme

Application Procedure

If you are interested in this vacancy, you can apply by clicking on the button above. By clicking on apply, you agree to our privacy commitment and terms and conditions . Your application will be sent directly to the recruiter in charge. IMPORTANT: if you are not yet registered with Undutchables we kindly ask you to do so. Your information will be handled in the strictest confidence and your CV will not be sent to a company unless you have given prior permission. Curious about how the recruitment process works within Undutchables, click here to read more.

Over de vacature

As Senior Associate Contracts & Pricing, you will act as an important link between different departments and international affiliates. When local teams negotiate contracts and prices, you help make sure these agreements are correctly translated into systems and processes. This is *not a role in which you will draft or negotiate contracts yourself

• . Instead, you will be the operational expert and advisor who makes sure contracts and pricing processes are followed correctly and lead to the expected results in areas such as orders, payments and revenue recognition. Your responsibilities will include:

• Acting as a main point of contact for international affiliates regarding contracts and pricing processes;
• Supporting colleagues with operational questions, issues and requests and helping them find the right solution;
• Making sure contract and pricing information is correctly processed and set up in the relevant systems;
• Working closely with departments such as Finance, Accounting, Commercial, Supply Chain and Operations;
• Supporting governance and ensuring procedures, documentation and controls are followed correctly;
• Helping maintain accurate and audit-ready processes;
• Analysing processes and identifying opportunities to improve efficiency, consistency and compliance;
• Supporting process changes, system improvements and international projects;
• Creating and maintaining process documentation, procedures, training materials and Quick Reference Guides;
• Providing training and guidance to business users;
• Analysing operational data and using your findings to support business decisions;
• Sharing best practices across countries and teams.

You will work extensively with *SAP and Vistex

• , a solution integrated with SAP that supports pricing and contract-related processes. Previous Vistex experience is not required, but you should be comfortable working with business systems and able to learn new tools quickly. #

Requirements

For this position, we are looking for someone who enjoys working in a structured international organization and is comfortable taking responsibility for their own work. You learn quickly, ask the right questions and don't simply work based on assumptions.You bring: - A Bachelor's/Master's degree with at least 2 years of relevant professional experience, or an Associate's degree with at least 5 years of relevant experience;

• Experience within a corporate, preferably multinational, organization;
• Relevant experience within areas such as contracts & pricing, finance, business administration, commercial operations or Order to Cash;
• Experience working with multiple stakeholders across departments such as Finance, Commercial, Supply Chain and Operations;
• Good understanding of business processes and preferably financial/accounting processes;
• Experience with SAP is strongly preferred;
• Strong Excel and PowerPoint skills and experience working with reporting tools;
• Fluent English communication skills.
• Experience within the *pharmaceutical or biotechnology industry

• is an advantage. Experience from another highly structured and regulated environment, such as medical devices or food, can also be relevant.

• Experience with *Vistex and/or Tableau

• is considered a plus, but is not required.

Benefits

• This is a *full-time position for 40 hours per week

• , initially for approximately one year via Undutchables. Depending on future business needs, there may be a possibility of extension.

• The standard working model is hybrid, with *Tuesday and Thursday as office days in Breda

• . During the first months, training and work-shadowing period, however, you should be prepared to work from the Breda office more frequently.

• Ideally, you are available to start around *mid-November or early December 2026

• .

• Travel reimbursement
• 30 Holidays
• Pension scheme

Application Procedure

If you are interested in this vacancy, you can apply by clicking on the button above. By clicking on apply, you agree to our privacy commitment and terms and conditions . Your application will be sent directly to the recruiter in charge. IMPORTANT: if you are not yet registered with Undutchables we kindly ask you to do so. Your information will be handled in the strictest confidence and your CV will not be sent to a company unless you have given prior permission. Curious about how the recruitment process works within Undutchables, click here to read more.

Over de vacature

This role is crucial for ensuring the quality and compliance of essential product documentation and master data. As a Quality Assurance Associate, you will play a vital part in safeguarding product integrity by meticulously reviewing and approving critical information. The ideal candidate will thrive in an environment that demands precision and a strong compliance mindset, contributing directly to the company's commitment to excellence.Your key responsibilities will include:

• Performing detailed quality reviews and approvals of artworks for various products.
• Conducting thorough quality checks and approvals for Bill of Materials (BOMs).
• Reviewing and approving critical fields within the master data system to ensure accuracy and compliance.
• Executing precise checks and verifying information against established procedures and regulatory standards.
• Collaborating effectively with team members to manage workload distribution and ensure timely completion of tasks.
• Identifying potential issues or discrepancies and proactively following up to ensure their resolution.
• Adhering strictly to Good Manufacturing Practice (GMP) guidelines and internal quality procedures.

Please note that we are unable to consider candidates who require visa sponsorship or who live too far from the work location. Candidates who would need to relocate can only be considered if they have already secured accommodation within a reasonable commuting distance. #

Requirements

We are looking for a highly detail-oriented and compliance-minded individual who is eager to contribute to a rigorous quality assurance process. You should possess a strong sense of responsibility, excellent communication skills, and a collaborative spirit to work effectively within a diverse team. The ideal candidate is proactive in identifying issues and committed to understanding the importance of accurate checks in a regulated environment. Character and mindset are paramount for success in this role. - English – C1 (spoken and written)

• Relevant educational background (e.g., Bachelor's or Master's degree in a scientific field)
• Some relevant in a regulated industry (e.g., Pharma, Food) is highly preferred
• Ability to perform highly detailed and precise review tasks
• Strong collaborative and communication skills
• Proficiency in standard office software; familiarity with SAP is a plus but not required

Benefits

• This is a 6-month contract position through Undutchables, with the possibility of future opportunities within the company, though no guarantees can be made for an extension in this specific role.
• Working hours: Full-time (40 hours/week) is preferred, but 32 hours/week is also an option.
• Hybrid work model: During the initial training period (approx. 1.5 months), you will be expected to be on-site 3-4 days per week. After training, a minimum of 2 days per week on-site is required, with Thursdays being a fixed office day.
• Competitive salary package.
• Pension scheme
• Travel expense reimbursement, dependent on distance.
• Dynamic, international, and collaborative work environment with excellent development opportunities.

Application Procedure

If you are interested in this vacancy, you can apply by clicking on the button above. By clicking on apply, you agree to our privacy commitment and terms and conditions . Your application will be sent directly to the recruiter in charge. IMPORTANT: if you are not yet registered with Undutchables we kindly ask you to do so. Your information will be handled in the strictest confidence and your CV will not be sent to a company unless you have given prior permission. Curious about how the recruitment process works within Undutchables, click here to read more.