Quality Assurance Officer: GMP & Compliance

SLS Services Limited

Birmingham

On-site

GBP 28,000 - 36,000

Full time

10 days ago
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Job summary

SLS Services Limited in Birmingham is seeking a quality professional to ensure GMP/GDP compliance and oversee the company's Quality Management System within a fast-paced pharmaceutical environment. You will perform internal audits, manage CAPA, approve materials, and maintain manufacturing documentation, contributing to product quality and patient safety.

This onsite, full-time role requires a degree in Pharmaceutical Sciences and at least six months' GMP experience, with MHRA standards

Qualifications

  • Bachelor's degree in Pharmaceutical Sciences or related discipline.
  • Minimum 6 months’ experience in a GMP-regulated pharmaceutical environment.
  • Solid understanding of QMS, SOPs, validation protocols, and regulatory guidelines.
  • Experience with internal audits, supplier assessments, and CAPA systems.

Responsibilities

  • Ensure compliance with statutory regulations and GMP/GDP requirements. Implement and maintain the company’s Quality Management System.
  • Investigate non-compliance issues and manage corrective actions.
  • Approve raw materials, intermediates, and finished products.
  • Organize and audit manufacturing documentation and records.
  • Perform internal audits and manage change control procedures.
  • Oversee validations for equipment, facilities, and processes.

Skills

GMP Compliance
QMS Knowledge
Internal Audits
CAPA Management
Documentation Review
Regulatory Awareness
HVAC Knowledge

Education

Bachelor's degree in Pharmaceutical Sciences

Tools

HVAC Systems

Job description

SLS Services Limited in Birmingham is seeking a quality professional to ensure GMP/GDP compliance and oversee the company's Quality Management System within a fast-paced pharmaceutical environment. You will perform internal audits, manage CAPA, approve materials, and maintain manufacturing documentation, contributing to product quality and patient safety.

This onsite, full-time role requires a degree in Pharmaceutical Sciences and at least six months' GMP experience, with MHRA standards

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