Senior Quality Systems Specialist
This an opportunity for a Senior Quality Systems specialist in the Pharmaceutical industry to join a reputable company in the Surrey area. As the Quality Systems Specialist, you will be responsible for managing all systems used on-site, ensuring compliance to GxP standards. KEY DUTIES AND RESPONSIBILITIES: Your duties as the Quality Systems Specialist will be varied however the key duties and responsibilities are as follows: 1. You will manage and develop the Quality Systems in place. This will include ensuring that the Trackwise document training systems, and Computer Software systems are controlled and validated. 2. As the Quality Systems Specialist, you will provide computer systems support during regulatory and client audits. You will ensure readiness prior to audits by reviewing and approving computer system compliance documentation, and post audit will monitor and manage CAPAs. 3. You will have the opportunity to learn Quality Assurance skills on a regional level. 4. You will lead and drive computer system Quality compliance throughout the business, ensuring a framework is implemented for computer systems use. This includes producing SOPs and training material for staff. ROLE REQUIREMENTS: To be successful in your application to this exciting opportunity as the Quality Systems Specialist we are looking to identify the following on your profile and past history: 2. Proven industry experience within a Pharmaceutical or Bio-technology environment, managing Quality Systems. 3. A working knowledge and practical experience with regulatory guidelines, such as GAMP5, Annex 11 Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer that is happy to welcome applications for any applicant who fulfil the role requirements for this position. HRS is a company exclusively supporting the science and technology sectors and is made up of a collaboration of scientists supporting science. We look forward to helping you with your next career moves.