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| Job Location | South West London |
| Education | Not Mentioned |
| Salary | £30,000 - £35,000 per annum |
| Industry | Not Mentioned |
| Functional Area | Not Mentioned |
| Job Type | Permanent, full-time |
We are currently looking for a QA Specialist to join a leading Pharmaceutical company based in the South West London area. As the QA Specialist, you will be responsible for maintaining cGMP compliance across the business function.KEY DUTIES AND RESPONSIBILITIES:Your duties as the QA Specialist will be varied. However, the key duties and responsibilities are as follows:1. You will play an active role in the Supplier Qualification and Management, liaise with Contract Manufacturing Organisations (CMOs) and other service providers in the negotiation of Quality Technical Agreements (QTAs).2. As the QA Specialist, you will raise and investigate Deviations through Root Cause Analysis (RCA), handle Customer Complaints, and implement and manage CAPAs and Change Controls.3. It will be your responsibility to participate in internal audits, client audits and regulatory inspections, seeking continuous quality improvements across the site.4. As the QA Specialist, you will provide GMP training to your colleagues, maintain an on-site QMS, produce batch manufacturing records, and conduct Product Quality Reviews (PQRs) to keep the business and products GMP compliant.ROLE REQUIREMENTS:To be successful in your application to this exciting opportunity as the QA Specialist, we are looking to identify the following on your profile and history:1. Relevant Life Science Degree.2. Proven industry experience in Quality Assurance in a Generics Pharmaceutical GMP environment.3. A working knowledge and practical experience with Quality Management Systems (QMS), Tech Transfers and New Product Introduction (NPI).Key Words: Quality Assurance | QA | Good Manufacturing Practice | cGMP | GMP | Pharmaceutical | Generics | Quality Management Systems | QMS | Tech Transfer | New Product Introduction | NPI | Compliance | CAPA | Change Control | Deviations | Supplier Qualification | Supplier Management | Internal Audits | External Audits | Client Audits | Regulatory Inspections | Root Cause Analysis | RCA | Product Quality Review | PQR | Batch Records