Job Overview
The role of Quality Specialist is a critical position that requires a high level of expertise in ensuring the accuracy and up-to-dateness of training documentation. This involves collaborating with various teams to maintain compliance and quality standards.
As a key member of the QA team, you will be responsible for reviewing and authoring technical documents, including SOPs, protocols, and reports. Additionally, you will provide support and troubleshooting for systems, assist with deviations, investigations, and change controls, and collaborate across departments to meet documentation and compliance needs.
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Key Responsibilities:
* Ensuring training documentation is current and accessible.
* Reviewing and authoring technical documents, including SOPs, protocols, and reports.
* Providing support and troubleshooting for systems.
* Assisting with deviations, investigations, and change controls.
* Collaborating across departments to meet documentation and compliance needs.
Requirements:
The ideal candidate will possess a Bachelor's degree in pharmaceutical, biological, or similar field, along with 2+ years of experience in the pharmaceutical industry.
Randstad encourages applications from individuals of all ages & backgrounds. Whilst appointments will be made on merit alone, candidates must be able to prove their right to work in the UK or the Republic of Ireland (as relevant).