Find jobs in pharmaceutical quality assurance (QA) and quality control. Includes jobs requiring GCP, GLP, GMP.
Quality Assurance jobs in Belgium (6), Bulgaria (1), Croatia (1), Czech Republic (1), Denmark (3), France (5), Germany (3), Hungary (1), Ireland (7), Multiple Countries (3), Netherlands (4), Poland (1), Spain (1), Switzerland (7) and United Kingdom (8).
Lead, coach, and develop Bioanalytical Study Management scientists as one integrated team, including goal setting, performance enablement, development planning, engagement, role clarity, and accountability for delivery; Set and drive the strategy for
You will act as a trusted quality and compliance advisor. You will help teams navigate complex regulatory requirements, strengthen quality processes, manage risk and continuously improve the way clinical trials are delivered. Monitor the regulatory
In this role, you will help ensure that our medical device products and quality processes meet applicable regulatory requirements and international standards. Working closely with colleagues across product development and the wider organization, you will
Provide QA support and expertise to iPSC cell culture, cell banking, cell differentiation in bioreactor and aseptic manufacturing activities; Maintain a strong QA presence on the shop floor and promote a proactive, right-first-time quality culture;
In this role, you will serve as the primary scientific and operational lead for outsourced quantitative bioanalytical activities at Contract Research Organisations (CROs) ensuring high-quality assay execution, regulatory compliance
Provide clearly defined Quality expectations and a Quality strategy for the assigned program(s) within the BioNTech product portfolio; Critically evaluate new products and processes with respect to Quality and compliance requirements. Work with
Support the Drug Linker Development Organization Head in the ramp up phase of the Accelerate Asset Development unit by defining and supporting the implementation of all critical business processes for drug linker projects; Manage the hiring process of the
Develop Manufacturing Industrial Strategic Supply Plans for Drug Products throughout their lifecycle, aligned with the broader supply-network strategy; Build and oversee the strategic industrial project portfolio covering launches, lifecycle management,
You will play a central role in translating CMC strategy into operational execution for development programs. You will be responsible for planning, coordinating, and driving day-to-day CMC activities while ensuring alignment across internal functions,
Responsible for leading a team of development engineers in the design, development, and lifecycle support of personalized and standard medical devices, including 3D-printed surgical guides and implants. This role combines technical leadership
Ensuring the sterility of injectable products through robust contamination control and sterility assurance strategies. This role extends beyond microbiological testing to encompass comprehensive oversight of aseptic manufacturing
Develop purification processes for active ingredients or intermediates ranging from the gram scale to several tens of kilograms (preparative liquid chromatography, batch, SFC, and SMB). Serve as the primary point of contact within your entity, ensure
You will identify compliance gaps, guide investigations, and lead improvements that support reliable laboratory processes. You will also share your expertise and help teams prepare for regulatory inspections. Lead improvement projects with QC, Quality
As the key figure overseeing product quality and harmonisation of our Quality Management System, you will play a pivotal role in ensuring our manufacturing processes meet the highest standards. Reporting directly to the Senior Director of Quality and
Provide technical leadership and mentorship to a diverse team with expertise in pharmaceutical formulation, process development, scale-up, and manufacturing support for synthetics drug products. Lead, develop, and inspire a multidisciplinary Drug Product
Responsible for leading and advancing the Clinical Quality Risk Management (QRM) framework, to strengthen clinical quality governance and support clinical program-level risk oversight. The role ensures that risk-based quality management principles are