Gmp Qa Specialist – On-Site/Hybrid Pharma Quality
O
Oxford Global Resources
📍 les, kingdom of spain, Spain
Job Description
Corporate QA Specialist (Pharma)
Desplácese hacia abajo para encontrar los detalles completos de la oferta de trabajo, incluyendo la experiencia requerida y las funciones y tareas asociadas.
Location: Sant Cugat (on-site). Start: ASAP. Full-time, long-term project.
Oxford Integral Resources – Life Sciences Unit is supporting one of the fastest-growing pharmaceutical companies headquartered in Spain, recognized for its strong commitment to innovation and R&D excellence.
We are currently looking for an experienced QA Specialist to join as a consultant in their Quality Assurance team on a long term project basis.
Reporting to the QA Manager, the role is responsible for ensuring compliance with our client’s internal policies and applicable regulatory standards, including Pharmaceutical Quality System requirements, Good Manufacturing Practices (GMP), Good Distribution Practices (GDP), Good Clinical Practices (GCP), Good Pharmacovigilance Practices (GVP), ISO 13485, ...
Desplácese hacia abajo para encontrar los detalles completos de la oferta de trabajo, incluyendo la experiencia requerida y las funciones y tareas asociadas.
Location: Sant Cugat (on-site). Start: ASAP. Full-time, long-term project.
Oxford Integral Resources – Life Sciences Unit is supporting one of the fastest-growing pharmaceutical companies headquartered in Spain, recognized for its strong commitment to innovation and R&D excellence.
We are currently looking for an experienced QA Specialist to join as a consultant in their Quality Assurance team on a long term project basis.
Reporting to the QA Manager, the role is responsible for ensuring compliance with our client’s internal policies and applicable regulatory standards, including Pharmaceutical Quality System requirements, Good Manufacturing Practices (GMP), Good Distribution Practices (GDP), Good Clinical Practices (GCP), Good Pharmacovigilance Practices (GVP), ISO 13485, ...