QA Manager

Science Solutions Recruitment Ltd; Guildford; Sur place; GBP 60 000 - 90 000; Plein temps

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

Quality Assurance Manager - UK - Onsite

Working within the unique and highly regulated radiopharmaceutical industry, this role offers the opportunity to make a genuine impact on products that support vital diagnostic and treatment pathways. As Quality Assurance Manager, you'll lead site quality activities, oversee GMP compliance, and help drive a culture of quality excellence within a specialist manufacturing environment.

Key Responsibilities

• Act as the site Quality Assurance lead, providing quality oversight across manufacturing, testing, and operational activities.
• Lead and develop the QA team, managing performance, training, workload planning, and staff development initiatives.
• Ensure the site Quality Management System remains compliant with GMP requirements and industry best practices.
• Review and approve quality events including deviations, CAPAs, change controls, complaints, OOS and OOT investigations.
• Drive continuous improvement initiatives and support the implementation and enhancement of eQMS and LIMS platforms.
• Lead internal audit programmes and support supplier, contractor, client, and regulatory inspections.
• Maintain oversight of data integrity practices and ensure appropriate controls and assessments are implemented.
• Review and approve quality documentation including SOPs, risk assessments, validation documentation, and site quality records.
• Support product introductions, validation activities, and cross-functional projects from a QA perspective.
• Lead site inspection readiness activities and act as a key contact during MHRA and customer audits.
• Monitor regulatory developments and ensure quality systems remain aligned with evolving GMP requirements.
• Work closely with operational teams to ensure effective contamination control strategies and ongoing compliance across the site.
• Support quality defect investigations, recalls, and escalation of critical quality issues where required.
• Promote a strong quality culture through coaching, mentoring, and training across the wider business.

Requirements

• Degree in a scientific discipline or equivalent pharmaceutical industry experience.
• Minimum of 5 years' Quality Assurance experience within a GMP-regulated pharmaceutical environment.
• Previous leadership, supervisory, or people management experience as well as experience in an aseptic/sterile environment is imperative.
• Strong working knowledge of GMP, quality systems, and regulatory compliance requirements.
• Experience managing deviations, CAPAs, change controls, audits, and validation activities.
• Excellent communication and stakeholder management skills.
• Strong organisational skills with a proactive approach to problem solving and continuous improvement.
• Experience supporting regulatory inspections and customer audits.
• Proficiency in Microsoft Office applications and electronic quality management systems