Job Title: Regional Quality Officer
Location: Slough or Bedford
Job Type: Full-Time | Permanent
Working Hours: 37.5 hours/week (Standard office hours)
Level: Mid-Level (Level 2)
Reports to: Regional Quality Manager / Quality Manager & RP
About the Role:
We are seeking a dedicated Regional Quality Officer to support quality operations across distribution centres in the South of England. This position is ideal for candidates with a strong background in quality assurance within regulated environments, particularly in warehousing and transport linked to the pharmaceutical or healthcare sectors.
You will play a vital role in upholding compliance with regulatory and international standards, including Good Distribution Practice (GDP), ISO 9001, ISO 13485, and ISO 14001. The role combines both on-site and remote support for quality processes, with some travel and overnight stays expected.
Key Responsibilities:
- Ensure ongoing compliance with GDP, ISO9001, ISO13485, ISO14001 and internal quality management systems.
- Provide day-to-day quality support and guidance across regional distribution centres.
- Conduct site inspections, quality tours, and Gemba walks with operations teams.
- Raise and manage deviations, non-conformances, CAPAs, and associated investigations.
- Carry out root cause analysis and effectiveness checks of corrective actions.
- Facilitate risk assessments and trend analysis across GDP and QA processes.
- Manage and review temperature-controlled storage and transport monitoring systems.
- Oversee quarantine processes and release activities for storage and transport consignments.
- Support qualification and mapping activities for warehouses, vehicles, and passive shipping systems.
- Conduct internal audits, support external audits and client visits, and provide documented audit responses.
- Review and update SOPs, work instructions, and quality documentation.
- Sign off on pest control inspections and temperature excursions.
- Deliver quality-related training to teams and contribute to continuous improvement initiatives.
Required Skills & Experience:
Essential:
- Minimum 3 years’ experience in a Quality function certified to ISO9001 or ISO13485.
- Background in Pharmaceutical, Healthcare, or regulated industries.
- Strong understanding of Good Distribution Practice (GDP).
- ISO9001 internal auditing experience.
- Confident with Quality Management Systems (QMS).
- Proficient in MS Office applications – Excel, Word, Visio, PowerPoint, Outlook.
- Highly organised, detail-focused, and able to work autonomously or in a team.
- Strong written and verbal communication skills for engaging with internal and external stakeholders.
Desirable:
- QMS Lead Auditor certification.
- Certified training within GxP.
- Capability or ambition to progress into Deputy Responsible Person (RP) responsibilities.
Additional Information:
- Role requires occasional travel between sites and overnight stays when necessary.
- This is a dynamic role best suited to individuals who thrive in fast-paced, compliance-focused environments and can balance technical knowledge with cross-functional collaboration.