Qualified Person (Radiopharma) Nottingham
Location: Nottingham, United Kingdom
Responsibilities
* Product Certification & Compliance: Certify and release batches according to UK and EU GMP, ensuring full compliance with regulatory standards and documentation.
* Quality Assurance: Oversee quality control tests, manage deviations, and maintain a high standard in manufacturing, testing, and supply chain documentation.
* Quality System Management: Lead the Quality Management System (QMS) at the site, collaborating with UK and European quality teams to uphold consistent, compliant practices.
* Collaborative Support: Act as a back‑up QP for Nottingham’s site when needed, ensuring seamless quality management and regulatory compliance.
Qualifications
* Qualifications: Degree in Life Sciences; eligible to act as a Qualified Person in the UK/EU.
* Core Skills: Strong problem‑solving, effective communication, and detailed knowledge of GMP regulations.
* Experience: Familiarity with quality management across the full pharmaceutical lifecycle.
Benefits
* 26 days of holidays
* Flexible benefits, including medical cover
* Pension contribution (match up to 10%)
* Company shares
Equal Opportunity Employer
As an equal opportunity employer, we welcome applications from individuals with disabilities.
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