Our client, a leading pharmaceutical company, is looking for a Co-Development Technician to support multiple clinical projects. This role ensures that clinical batches and critical samples are supplied on time to clinical studies, packaging sites, and testing laboratories worldwide.
Our client, a leading pharmaceutical organization, is seeking an R&D Method Development & Validation Specialist to support their analytical operations. This role focuses on developing and validating robust analytical methods using state-of-the-art statistical approaches to ensure scientific excellence.
Our client, a leading pharmaceutical company, is seeking a QA Specialist to support their development analytical laboratories. This transversal role focuses on providing quality oversight and scientific partnership within analytical development and clinical supply operations.
Our client, a leading pharmaceutical company, is seeking a Cleaning Validation Engineer to specialize in the development and optimization of cleaning processes for production equipment. The role combines technical expertise with operational support to ensure compliance and business continuity within a regulated manufacturing environment.
Our client, a global pharmaceutical leader, is seeking an Associate Clinical Project Manager to provide comprehensive operational support in delivering clinical studies. This role involves managing the study lifecycle from protocol development through to archiving, ensuring all quality, timeline, and regulatory objectives are met.
Our client, a leading pharmaceutical company, is seeking a CSV Validation Engineer to join their team. This role focuses on the validation of software packages and computerized systems to ensure compliance with global regulatory standards.
Our client, a global life sciences organization, is seeking a Quality Performance Lead to play a pivotal role within a major quality management system transformation. This role focuses on the end-to-end design and implementation of a quality performance framework and KPI pyramid to drive data-driven decision-making.
Our client, a leading pharmaceutical organization, is seeking a Sterility Assurance Manager. This role focuses on developing and overseeing the sterility assurance program to maintain safety and regulatory compliance in vaccine production. The position serves as a technical expert in microbiology and aseptic processes to drive continuous improvement across manufacturing units.
Our client, a leading pharmaceutical company, is seeking a Senior Specialist Microbiology to serve as a project manager within their quality organization. This role involves managing complex microbiological topics and ensuring high standards of compliance and safety.
Our client, a leading pharmaceutical company, is looking for a Commissioning Lead to drive the execution of an ambitious project. This role involves overseeing the entire commissioning lifecycle, bridging the gap between engineering, contractors, and quality departments to ensure successful delivery of critical installations.
Design, implement, and validate digital systems that support GMP manufacturing, ensure data integrity, and enable efficient, compliant operations across life sciences environments.
MES Consultant – Implement and optimize MES to support efficient, compliant manufacturing.
CSV Consultant – Validate GxP systems and ensure regulatory-compliant digital solutions.
MES Specialist – Configure and maintain MES to support production operations.
MBR Editor – Create and update accurate electronic batch records.
MBR Designer – Design structured, compliant electronic batch workflows.
MBR Reviewer – Review and approve electronic batch records for accuracy.
Master Batch Editor – Maintain and update Master Batch documentation.
Master Batch Reviewer – Ensure GMP-compliant batch record quality.
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