System Administrator
* Collaborate with system owners to design and maintain compliant, efficient quality systems supporting product lifecycle.
* Oversee data integrity and act as system administrator for key Quality Systems. Ensure compliance with regulatory requirements.
* Evaluate, approve, and monitor suppliers, including managing quality agreements.
* Lead change control processes and handle regulatory submissions. Support inspection readiness programs.
* Review and approve analytical method transfers, protocols, and related investigations.
* Manage GMP documentation, site validation plans, and the development of the site training system for GMP activities.
Requirements
* Bachelor's degree in pharmaceutical, biological, or similar field.
* 4+ years of experience in the pharmaceutical industry.
* Ability to work in a dynamic environment and prioritize tasks effectively.
Individuals from all ages & backgrounds are encouraged to apply. Candidates must be able to prove their right to work in the UK or the Republic of Ireland (as relevant).