At MindCapture you are not just starting a new role. You are joining a community that invests in your development and gives you the opportunity to grow in a meaningful technical career within healthcare.
You can count on:
- A competitive salary with a full benefits package including meal vouchers, eco vouchers, health insurance, group insurance, net expense allowance and a company car with charging or fuel card
- Personal growth support with tailored training and clear career development
- A stable environment where your technical skills directly contribute to improved patient care
- The chance to work with high tech diagnostic systems at top tier healthcare institutions
- A warm and collaborative culture focused on trust, ownership and long term impact
In this role, you will perform quality control testing on raw materials and finished products within a pharmaceutical laboratory environment. You will analyse samples using established analytical techniques, interpret results and document your findings accurately. Working according to GMP requirements and quality procedures, you will also contribute to maintaining analytical methods and a safe, efficient laboratory environment.
Key responsibilities
- Quality control testing: Perform analytical testing on raw materials and finished products
- Sample analysis: Analyse samples using HPLC, GC, IR and UV techniques
- Result interpretation: Evaluate analytical results and report findings clearly and accurately
- GMP compliance: Perform laboratory activities according to GMP requirements and quality procedures
- Analytical methods: Document, maintain and update analytical methods
- Laboratory safety: Contribute actively to a safe and efficient laboratory environment
Required competences & skills
- Education: Bachelor degree in Chemistry, Pharmaceutical Laboratory Technology or an equivalent qualification
- Experience: Minimum 1 year of professional quality control experience
- Analytical techniques: Practical experience with HPLC and GC is required
- Languages: Professional proficiency in Dutch and English at minimum B2 level
- Shift work: Willingness to work in a two shift system
- Pharmaceutical experience: Previous experience within the pharmaceutical industry is required
- GMP documentation: Knowledge of GMP documentation is required
- Method validation: Experience with analytical method validation is a plus
Quality & Compliance Wetteren Junior At MindCapture as consultant
About this application
This opportunity is offered through MindCapture as a consultancy role with strong day to day ownership. You will be placed on site with our client.
MindCapture supports you throughout your assignment with clear onboarding, regular follow up and access to learning opportunities. You will have a dedicated point of contact, transparent communication and support to help you deliver impact in a structured way.
Job Contact – Talent & Business Team
Our Talent & Business Managers combine a deep understanding of our clients’ needs with a sharp eye for talent. Their focus is on creating meaningful and sustainable matches, always keeping both the role and the candidate in mind.
When a potential match is identified, one of our T&B colleagues may reach out to answer your questions, share additional context about the role and discuss possible next steps together, with clarity and transparency throughout the process.
How our application process works
- Apply online – Submit your application in just a few clicks.
- Personal interview – If we see a potential match, our team reaches out to get to know you better, explore your skills and ambitions and hear what you value in your next challenge.
- Client introduction – We match you with potential projects and introduce you to clients where your expertise fits best.
- Client interview & feedback – You meet with the client to explore project details and expectations, while we support you throughout the discussions and provide follow-up afterwards.
- Final interview & welcome – In a final chat with our team, we close the process and warmly welcome you to MindCapture, guiding you towards a smooth start with us or at the client site.
Explore other jobs in Quality & Compliance
- Support global change controls for manufacturing processes
- Coordinate stakeholders across quality and operations
- Enable tech transfers and continuous improvement
- Drive process verification within cell therapy manufacturing
- Analyse manufacturing data to identify trends
- Strengthen governance through monitoring and investigation
- Maintain compliant industrial IT systems within operations
- Coordinate validation, maintenance and investigations
- Bridge operational technology, IT, quality and business
- Review qualification documentation using risk based methods
- Support compliance, investigations, audits and CI
- Perform quality control within a regulated environment
- Analyse samples using analytical techniques
- Ensure accurate documentation while following GMP
- Take ownership of broad QA responsibilities in GMP
- Manage deviations, audits and compliance related activities
- Drive quality improvements through investigations
- Provide quality oversight for cleaning validation activities
- Ensure compliance across validation processes
- Guide stakeholders on risk based quality decisions effectively
- Lead quality assurance in a growing biopharma environment
- Strengthen compliant quality systems
- Guide audits and improvement initiatives
- Execute validation of GMP critical computerised systems
- Ensure compliance with FDA and EU regulatory standards
- Generate validation documentation and resolve issues
- Maintain and troubleshoot lab equipment in GMP setting
- Ensure compliance with cGMP standards and safety guidelines
- Support upgrades and continuous improvement initiatives
- Perform QC testing for cell therapy products
- Ensure compliance with GMP and regulatory standards
- Collaborate on tech transfer and quality documentation
- Drive quality strategy for global computerised systems
- Ensure validation in line with GMP requirements
- Lead audits, inspections and compliance risk assessments
- Build, implement and maintain Quality Management Systems
- Manage deviations, CAPAs and change control processes
- Prepare for and support audits and inspections