Description:
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
