This list contains only the countries for which job offers have been published in the selected language (e.g., in the French version, only job offers written in French are displayed, and in the English version, only those in English).
We are seeking a structured, development-oriented, and quality-driven Head of QC and Warehouse to lead and further strengthen our Quality Control function and GMP warehouse operations as Minerva Imaging continues to grow. This role combines strong scientific expertise with leadership responsibility with a strong focus on process optimization, operational development, and continuous improvement across QC and warehouse activities., ensuring full compliance with GMP requirements. We are looking for a highly structured, detail-oriented and quality-focused leader who thrives in a GMP-regulated environment. You work systematically and compliance-driven, while also having a strong ability to identify opportunities for optimization and implement improvements that enhance efficiency, quality, and scalability. You are motivated by creating robust processes, driving operational excellence, and ensuring that workflows support both compliance and business growth. You bring a strong leadership presence and communicate clearly and effectively, translating complex quality requirements into practical and workable solutions for your team, and report directly to the Head of CDMO. You naturally take ownership and initiative, driving projects, improvements, and decision-making forward. With a pragmatic and solution-oriented mindset, you actively identify opportunities for development and continuous improvement. At the same time, you build strong and trust-based relationships across the organization and with external partners, including customers and sponsors.
Job Responsibility:
Lead and develop the QC function and GMP warehouse, including a team of scientists and laboratory technicians
Ensure all QC and warehouse activities are compliant with GMP standards and regulatory requirements
Maintain overall responsibility for QC quality systems, including deviations, CAPA, and change control
Review and approve QC documentation and analytical data
Ensure proper handling, storage, and release of materials within the GMP warehouse
Drive process optimization and operational development initiatives, including implementation of new systems, digital tools, workflows, and continuous improvement projects
Participate in audits and ensure audit readiness
Oversee maintenance, qualification, and optimization of QC equipment and laboratory processes
Requirements:
Minimum 5 years of GMP experience within a QC environment
Proven leadership experience within QC, including people management
Strong experience with process optimization, operational development, or continuous improvement initiatives within a regulated environment
Hands-on experience with analytical methods and equipment (e.g., HPLC, GC, ICP-OES)
Experience with method validation is required and microbiology experience is a strong advantage
Relevant academic background (this could be MSc in Chemistry, Biochemistry, Biotechnology, Pharmacy, or similar)
Strong understanding of GMP processes, quality systems, and operational workflows
Fluent in English, both written and spoken
What we offer:
flexible working options including the option of working from home
health insurance
quality conscious lunch scheme
monthly social activities
informal organization with a strong focus on open and honest communication