Walker Cole International is supporting a leading pharmaceutical manufacturer with the search for a QA Specialist to join their Quality Assurance function in North West England.

This is an excellent opportunity to join a growing organisation during an exciting period of investment and operational development, supporting GMP compliance across a complex manufacturing environment.

Key Responsibilities for the QA Specialist:

• Provide QA oversight for documentation, systems and processes during facility start-up and ongoing operations
• Support batch record review, deviations, CAPAs, change controls and quality investigations
• Represent QA within site projects, audits and regulatory inspections
• Drive GMP compliance and continuous improvement activities across the site

Requirements for the QA Specialist:

• Experience within a QA role in a pharmaceutical or biopharmaceutical environment
• Strong understanding of GMP regulations and pharmaceutical quality systems
• Experience supporting quality investigations and batch review activities
• Sterile manufacturing experience would be highly advantageous

GMP | Quality Assurance | QA Specialist | Batch Review | Batch Release | Deviations | CAPA | Change Control | Pharmaceutical Manufacturing | Sterile Manufacturing | QMS | Quality Systems | GDP | Root Cause Analysis | Regulatory Compliance | MHRA | Validation | Audits | Investigations | SOPs | Continuous Improvement | Biopharmaceutical | GMP Documentation | Risk Management | Quality Events | Pharmaceutical QA