Planet Pharma are currently partnered with a global biopharmaceutical company and we are actively seeking a QA Specialist II to join the team in Slough.
Key Responsibilities
- Support the rollout of new document management and quality record systems, including data clean‑up, preparation activities, validation support, and coordination with key stakeholders to ensure smooth adoption.
- Provide regular progress updates to management and contribute to the successful execution of system‑related initiatives.
- Monitor internal quality records to ensure timely completion and compliance with established processes.
- Assist in conducting deviations or investigations as required, ensuring accurate documentation and follow‑through.
- Carry out business‑related activities as assigned by leadership, contributing to departmental and organizational objectives.
- Take ownership of fostering a strong quality mindset and adherence to best practices across the organization.
Key Requirements
- Relevant scientific degree
We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.
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