QA Manager

MindCapture

Belgique

Sur place

EUR 90 000 - 130 000

Plein temps

Il y a 3 heures
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Avantages offerts par ce poste

Meal vouchers
Health insurance
Company car with charging or fuel card
Training opportunities
Eco vouchers

Résumé du poste

MindCapture is seeking an experienced QA Manager to lead quality activities across laboratory testing, outsourced manufacturing and quality systems in a regulated biopharma setting. You will maintain GMP compliance and support inspection readiness, with potential Qualified Person responsibilities when qualified.

You will manage the QA team, oversee quality records and drive continuous improvement, ensuring robust documentation and risk-based decision making in a dynamic pharmaceutical

Qualifications

  • Master's degree in pharmaceutical sciences or a related discipline.
  • At least ten years of QA management experience within GMP regulated pharmaceutical/biotechnology environments.
  • Five years of experience overseeing quality control laboratory activities, preferably involving biological products.
  • Five years of people management experience.
  • Strong knowledge of GMP, ICH, USP, and regulatory requirements; inspection experience.

Responsabilités

  • Lead QA team across laboratory testing, outsourced manufacturing and quality systems.
  • Maintain and continuously improve a compliant Quality Management System.
  • Ensure activities follow GMP requirements, procedures, specifications and quality agreements.
  • Lead vendor qualification, internal and external audits, and authority inspections.
  • Organise annual management reviews and monitor quality indicators.
  • Review methods, specifications, validations, protocols, reports and certificates.
  • Review deviations, change controls and corrective actions.
  • Approve equipment qualification and computerised system validation docs.
  • Establish GMP training systems and performance indicators.
  • Support regulatory inspection readiness and address findings effectively.

Connaissances

Team leadership
Quality management
GMP compliance
Audit management
Quality documentation
Communication
Regulatory knowledge
Training governance
Inspection readiness
Lab oversight

Formation

Master’s degree in pharmaceutical sciences
Biotech or related field

Outils

Quality Management System (QMS)
Validation software
Analytical instrumentation oversight

Description du poste

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

Take ownership of quality assurance leadership within a regulated biopharma setting.

Our client is seeking an experienced QA Manager to coordinate quality activities across laboratory testing, outsourced manufacturing and quality systems. You will lead the QA team, maintain compliance with current GMP requirements and support inspection readiness. The role may also include Qualified Person responsibilities for investigational medicinal products when the required qualifications are present.

Key responsibilities
  • Team leadership: Allocate resources, set priorities, plan activities and evaluate QA personnel
  • Quality systems: Implement, maintain and continuously improve a compliant Quality Management System
  • Compliance oversight: Ensure activities follow current GMP requirements, procedures, specifications and quality agreements
  • Audit management: Lead vendor qualification, internal audits, external audits and authority inspections
  • Quality review: Organise annual management reviews, monitor quality indicators and oversee corrective actions
  • Laboratory oversight: Review and approve methods, specifications, validations, protocols, reports and certificates
  • Quality records: Review deviations, change controls, corrective actions and atypical laboratory results
  • Validation oversight: Approve equipment qualification and computerised system validation documentation
  • Training governance: Establish GMP training systems, training plans and performance indicators
  • Inspection readiness: Support regulatory inspection preparation and ensure findings are addressed effectively
Required competences & skills
  • Education: Master’s degree in pharmaceutical sciences, bioengineering, biomedical sciences or a related discipline
  • Quality experience: At least ten years of QA management experience within a GMP regulated pharmaceutical or biotechnology environment
  • Laboratory oversight: At least five years overseeing quality control laboratory activities, preferably involving biological products
  • People management: At least five years of experience leading and developing teams
  • Regulatory knowledge: Strong knowledge of current GMP, European Pharmacopoeia, United States Pharmacopeia, ICH, WHO and relevant United States regulations
  • Inspection experience: Participation in health authority inspections, preferably involving European and United States authorities
  • Communication: Strong written and verbal communication, planning and organisational skills
  • Languages: Fluent written and spoken English with knowledge of Dutch
  • Leadership: Demonstrated ability to motivate teams, share expertise and support organisational development
  • Additional expertise: Experience with process performance qualification and biological licence submissions is a plus

Quality & Compliance Ghent 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.

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.

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  • Drive process verification within cell therapy manufacturing
  • Analyse manufacturing data to identify trends
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  • 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
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