GMP Quality Compliance Specialist

Adecco; Sutton Coldfield; On-site; GBP 21,000 - 26,000; Full time

Job summary

Adecco is recruiting two Quality Compliance Administrators for a temporary full-time role in Sutton Coldfield. The positions focus on quality assurance, SOP management, and GMP compliance across medicinal and non-medicinal products.

Successful candidates will support auditing, document control and Deputy Qualified Person duties, contributing to the organisation’s commitment to quality and regulatory standards.

Qualifications

• Strong understanding of quality assurance and control principles.
• Experience in preparing and maintaining SOPs.
• Familiarity with GMP and quality management systems.
• Excellent organisational skills and attention to detail.
• Proficiency in Microsoft Excel and associated software.
• A valid driving licence is advantageous for conducting audits.

Responsibilities

• Continuously improve current quality systems to enhance product and service quality.
• Prepare and maintain SOP documents.
• Ensure GMP compliance for stock management including quarantine, release, batch rotation, labelling and storage.
• Oversee document quality control including issuing, tracking and archiving.
• Collaborate with staff to ensure quality standards for medicinal and non-medicinal products.
• Establish quality requirements with external suppliers in partnership with purchasing.
• Conduct internal and third-party audits to ensure GMP compliance.
• Support Deputy Qualified Person duties including handling customer complaints and liaising with regulatory bodies.

Skills

Quality assurance principles

SOP preparation

GMP familiarity

Organisational skills

Attention to detail

Driving licence

Tools

Microsoft Excel

Job description

Adecco is recruiting two Quality Compliance Administrators for a temporary full-time role in Sutton Coldfield. The positions focus on quality assurance, SOP management, and GMP compliance across medicinal and non-medicinal products.

Successful candidates will support auditing, document control and Deputy Qualified Person duties, contributing to the organisation’s commitment to quality and regulatory standards.