QC Supervisor

At Mind Capture you are not just taking on a new job, you are joining a community that values who you are and what you bring to the table.

You can count on:

• The chance to work on healthcare projects that directly improve lives
• Competitive salary with a full package of extra-legal benefits including meal vouchers, eco vouchers, DKV health insurance, group insurance, net expense allowance and a company car
• Personalised training and development opportunities to shape your career path
• A supportive environment where you choose what you love to do, build on your strengths and make a difference where it matters most

This role strengthens operational quality control leadership.

Our client is a Belgian organisation active in the pharmaceutical industry with two sites in Puurs and a broad portfolio of non sterile medicines production plus packaging, supported by research plus development services. As QC Operational Supervisor you lead multiple QC teams and safeguard quality, efficiency plus compliance across operational QC activities, with clear ownership plus an improvement mindset.

Key responsibilities

• You will lead QC Operations while ensuring GMP aligned delivery.
• Team leadership:
  Manage multiple QC teams plus coach performance
• Daily operations:
  Plan organise plus follow up routine QC activities
• Compliance oversight:
  Ensure adherence to GMP safety plus quality procedures
• Method lifecycle:
  Own method transfers verifications plus validations
• Cross functional alignment:
  Collaborate with QA production plus supply chain stakeholders
• Audit readiness:
  Represent QC during audits plus health authority inspections
• External interface:
  Act as primary QC contact for customers plus external partners

• Master degree in pharmacy chemistry or biochemistry
• At least 5 years experience in Quality Control within a GMP environment
• First leadership experience with proven ability to lead teams
• Strong hands on experience with HPLC
• Solid knowledge of ICH guidelines plus analytical quality processes
• Experience with inspections by authorities such as national or international agencies

Quality & Compliance Puurs Senior Consultant at Mind Capture

This opportunity is offered through Mind Capture as a consultancy role with strong day to day ownership. You will be placed on site with our client.

Mind Capture supports you throughout your assignment with clear onboarding, regular follow up plus access to learning opportunities. You will have a dedicated point of contact, transparent communication plus support to help you deliver impact in a structured way.

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.

• 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 Mind Capture, guiding you towards a smooth start with us or at the client site.

• Experience in non sterile drug product manufacturing
• Experience leading multiple teams or shifts
• Strong stakeholder management with customers and partners
• Write CMC drug substance content for regulatory submissions
• Translate complex data into compliant documentation
• Align…