QA Manager - GMP Radiopharma Onsite Lead

Science Solutions Recruitment Ltd

Guildford

Sur place

GBP 60 000 - 90 000

Plein temps

Il y a 3 jours
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Résumé du poste

Science Solutions Recruitment Ltd is seeking a Quality Assurance Manager for an onsite UK role in the radiopharmaceutical sector. You will lead QA activities, ensure GMP compliance, and foster a culture of quality excellence across manufacturing and testing.

The candidate will have 5+ years in QA within GMP pharma, a science degree, and strong experience with deviations, CAPAs, change controls, audits, and regulatory inspections.

Qualifications

  • Degree in a scientific discipline.
  • Minimum of 5 years' Quality Assurance experience within a GMP-regulated pharmaceutical environment.
  • Leadership or people management experience in an aseptic/sterile setting is imperative.
  • Strong GMP knowledge and regulatory compliance experience.
  • Experience managing deviations, CAPAs, change controls, audits, and validation activities.

Responsabilités

  • Act as the site QA lead, providing quality oversight across manufacturing, testing, and operations.
  • Lead and develop the QA team, including performance management and staff development.
  • Ensure the site Quality Management System remains compliant with GMP requirements.
  • Review and approve quality events including deviations, CAPAs, change controls, complaints, OOS and OOT investigations.
  • Drive continuous improvement and support eQMS/LIMS initiatives.
  • Lead internal audits and assist with supplier, contractor, client, and regulatory inspections.
  • Maintain data integrity practices and enforce appropriate controls.

Connaissances

QA Leadership
GMP Compliance
Regulatory Compliance
Audit Management
CAPA & Deviation
Stakeholder Management
Documentation Control
LIMS/eQMS
Leadership

Formation

Science degree

Outils

LIMS
eQMS
MS Office

Description du poste

Science Solutions Recruitment Ltd is seeking a Quality Assurance Manager for an onsite UK role in the radiopharmaceutical sector. You will lead QA activities, ensure GMP compliance, and foster a culture of quality excellence across manufacturing and testing.

The candidate will have 5+ years in QA within GMP pharma, a science degree, and strong experience with deviations, CAPAs, change controls, audits, and regulatory inspections.

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