Top Tech Jobs & Startups Jobs

Le responsable du laboratoire de contrôles analytiques supervisera les activités du laboratoire, garantissant la qualité des résultats. Il/elle contrôlera la qualité des matières premières et produits finis, gérera une équipe, et assurera le respect des exigences des BPF.

Realizar processos manuais de produção, operar equipamentos simples e zelar pela segurança do paciente. Auxiliar no recebimento, conferência, transporte e armazenamento de materiais relacionados à produção na Catalent.

The Supervisor, Form Fill oversees daily activities in production, focusing on increasing efficiency and reducing waste. They manage a team, coordinate work activities, ensure safety and compliance with GMP standards, and lead continuous improvement initiatives.

Perform routine testing of process samples, raw materials, finished products, and stability samples in a cGMP compliant environment. Responsible for microbiology testing, data analysis, document writing, and reporting to support drug development programs. Execute Quality Control testing, author technical documents, and support process improvement initiatives. Bachelor's degree in a science field required.

The Quality Control Intern at Catalent will support the Quality Control team in ensuring that all manufactured products meet specified standards for quality and safety. Responsibilities include data analysis, process improvement, and maintaining communication with team members.

The Executive Sourcer plays a key role in identifying and attracting top-tier leadership talent for executive-level roles. Responsibilities include strategic sourcing, candidate identification, engagement, screening, data management, and providing strategic advisory. The candidate must have a Bachelor's degree, 2+ years of recruitment experience with emphasis on candidate research, fluency in French and English, and proficiency in Applicant Tracking Systems.

The Quality Assurance Associate will provide quality support to a Clinical Storage and Distribution facility in Singapore in line with PIC/S Good Manufacturing Practice and Good Distribution Practice. Responsibilities include material review and release, support on Quality matters, CAPA evaluation, Change Control review, validation document approval, batch record review, audit coordination, and more.