Quality Assurance Associate

We are looking for a detail-oriented and proactive Quality Assurance Associate to join an international pharmaceutical company in Breda.

In this role, you will be responsible for reviewing and approving SAP Master Data, Bill of Materials (BOM), and artwork for medicinal products. You will help ensure that all information is accurate, compliant, and meets the required quality standards.

The right mindset is more important than years of experience. Whether you are a recent graduate or already have experience in Quality Assurance, we are looking for someone who works accurately, takes ownership, and understands the importance of compliance. You will receive thorough training to become familiar with the processes and systems before working independently.

Your Responsibilities

• Perform QA review and approval of SAP Master Data, including critical value verification and Bill of Materials (BOM).
• Review and approve artwork for medicinal products, including packaging materials and labels.
• Ensure compliance with applicable quality standards and regulatory requirements.
• Create, review, and maintain operational Standard Operating Procedures (SOPs) and Work Instructions.
• Identify, investigate, and escalate data integrity or quality-related issues.
• Support QA-related projects, investigations, and continuous improvement activities.
• Prepare weekly and monthly performance metrics and maintain departmental performance boards.
• Collaborate with internal stakeholders, including the Global Artwork Center, Master Data, Supply Chain, Regulatory Affairs, and QA Management.

The position mainly involves detailed reviews, verification, and approval activities. You should therefore enjoy working in a structured environment where accuracy and attention to detail are essential.

What We Are Looking For

• An MBO, Bachelor’s, or Master’s degree in Life Sciences, Quality Assurance, or a related field.
• Junior candidates and recent graduates are welcome. Previous QA experience is an advantage but not a strict requirement.
• A strong quality and compliance mindset, with an understanding of the importance of following procedures.
• Excellent attention to detail and the ability to work accurately and systematically.
• Good communication skills and the ability to collaborate within an international team.
• A proactive attitude, with the ability to recognize, communicate, and escalate potential issues.
• Comfortable performing repetitive tasks that require a high level of concentration and accuracy.
• Ability to manage priorities and maintain quality under pressure.
• Fluency in English, both written and spoken.

About the Team
You will join an international Quality Assurance team of approximately 10 colleagues, with around 4 team members performing similar activities.
The team works closely together, shares responsibilities, and supports each other in maintaining high-quality standards.

Practical Information

• Contract duration: 6 months, with no guaranteed extension.
• Working hours: 40 hours per week.
• Training period: Approximately 1-1.5 months, requiring 3-4 days onsite per week.
• After training: Minimum 2 days onsite per week, mandatory onsite day is Thursday.
• Start date: As soon as possible. A notice period of approximately 1 month is acceptable.

Interested?
Are you accurate, eager to learn, and motivated to contribute to quality within the pharmaceutical industry? Whether you are starting your career or already have QA experience, we would like to hear from you!