Quality Systems Specialist (GMP)

Job description

About this role TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies across development and manufacturing. Our expertise includes full-service capabilities, resourcing, and Functional Service (FSP) solutions. The Quality Systems Specialist (GMP) is responsible for supporting and maintaining quality systems within a GMP-regulated pharmaceutical manufacturing environment. This includes ensuring compliance through audit activities, CAPA management, and effective quality system processes. As part of our SRS/FSP team, you will be dedicated to one sponsor, a global pharmaceutical company operating within a GMP-regulated manufacturing environment. Contract: 3-month consultancy: Key Responsibilities: Support and maintain Quality Management System (QMS) activities in line with GMP requirements Manage and follow up on CAPAs, ensuring timely closure and effectiveness Perform and support internal and supplier audits Support supplier qualification and ongoing supplier management activities Maintain GMP documentation, including document control and training records Participate in change control processes...