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
You will act as the primary QP contact for an assigned manufacturing area and provide QP oversight throughout quality and release processes. The role includes reviewing batch release dossiers, approving quality documentation, supporting regulatory submissions and releasing commercial and clinical lots within the ERP system.
Key responsibilities
- QP support: Act as the primary QP contact for issues within an assigned manufacturing area
- Quality oversight: Provide QP feedback to QA engineers and elevate relevant deviations or changes
- Batch documentation: Perform detailed review and approval of batch release dossiers
- Batch release: Release commercial and clinical lots in the ERP system for shipment
- Quality documentation: Review and approve Certificates of Analysis, deviations and Product Specification Sheets
- Regulatory submissions: Review and approve new or major updates to regulatory submissions
- Shipment approval: Approve specific product and sample shipments where QP authorisation is required
- Reference samples: Review and approve exceptional use, destruction or regulatory provision of reference samples
Required competences & skills
- Education: Master of Industrial Pharmacy
- QP qualification: Valid QP number according to applicable Belgian regulatory requirements
- Pharmaceutical experience: Minimum eight to ten years of experience within the pharmaceutical industry
- QP experience: Previous experience acting as a QP is a plus
- Biotechnology: Extensive knowledge and experience in biotechnology production processes
- Dutch: Fluent proficiency is required
- English: Fluent proficiency is required
Quality & Compliance Antwerp Senior 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.
Explore other jobs in Quality & Compliance
- Oversee facility and utility qualification
- Support QP oversight across manufacturing and release
- Review critical documentation for batch release activities
- Ensure regulatory compliance throughout quality
- 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