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Lead day-to-day Quality Control laboratory operations focusing on Microbiology, providing mentorship and ensuring compliance with GMP standards while managing stability, testing, and documentation processes.

The Manager, QC Systems will oversee the implementation and management of QC-related electronic systems, ensuring compliance with CMC/GMP regulations and enhancing data-driven laboratory operations. Responsibilities include maintaining quality management systems, managing eSystems for sample analysis and reporting, supporting system qualification, and collaborating cross-functionally to ensure quality standards are met.

The Specialist in QC Systems will manage and improve the Quality Management System (QMS) related to QC activities, ensuring compliance with CMC/GMP standards. This role supports electronic systems for lab operations and collaborates across functions for effective quality practices.

The job focuses on expanding teams in Protein Science, Drug Development, Manufacturing, Quality, and supporting roles in various scientific and engineering fields.

The Clinical Quality Manager oversees clinical trial quality assurance, ensuring compliance with regulations, conducting training, and managing corrective actions to enhance clinical processes.

Lead hands-on QC microbiology operations including bioburden, endotoxin, microbial ID, EM sampling, utilities monitoring, contamination investigations, and mentorship. Ensure GMP inspection readiness, oversee sample workflows, review microbiology documentation, and troubleshoot assays and deviations to maintain data integrity.

The Clinical Research Coordinator will support clinical trials, ensuring compliance with regulatory requirements while coordinating activities, documents, and communications throughout the trial phases.

Le gestionnaire des études cliniques planifie et supervise les études cliniques, en garantissant la conformité aux règlements, la qualité des données et le respect des délais et budgets.