| London Jobs |
| Manchester Jobs |
| Liverpool Jobs |
| Nottingham Jobs |
| Birmingham Jobs |
| Cambridge Jobs |
| Glasgow Jobs |
| Bristol Jobs |
| Wales Jobs |
| London Jobs |
| Manchester Jobs |
| Liverpool Jobs |
| Nottingham Jobs |
| Birmingham Jobs |
| Cambridge Jobs |
| Glasgow Jobs |
| Bristol Jobs |
| Wales Jobs |
| Oil & Gas Jobs |
| Banking Jobs |
| Construction Jobs |
| Top Management Jobs |
| IT - Software Jobs |
| Medical Healthcare Jobs |
| Purchase / Logistics Jobs |
| Sales |
| Ajax Jobs |
| Designing Jobs |
| ASP .NET Jobs |
| Java Jobs |
| MySQL Jobs |
| Sap hr Jobs |
| Software Testing Jobs |
| Html Jobs |
| Job Location | Fordham, Ely |
| Education | Not Mentioned |
| Salary | £30,000 - £45,000 per annum, inc benefits |
| Industry | Not Mentioned |
| Functional Area | Not Mentioned |
| Job Type | Permanent, full-time |
Quality Assurance Advisor, Fordham, - £30,000- £45,000k pa –My client is looking for a conscientious and articulate Quality Assurance Professional with a proven track record in a cross functional cGMP/GCP/GLP environment, to join them on a permanent basis.Position- Quality Assurance AdvisorLocation- FordhamSalary- £25,000 - £35,000Key responsibilities and accountabilities:• Demonstrates a strong knowledge of root cause analysis techniques• Able to plan, carry out and follow up on audits/self inspections• Able to perform QA audits/data pack review including those relating to CSV and Validation activities• Support and administration of system relating to equipment qualification• Audits and approves protocols and reports related to equipment Validation including CSV. This includes review of deviations reported during execution• Maintain knowledge in the current and relevant regulations and guidance in accordance with role demands and changes• Support external inspections, customer audits & enquiries as required• Work productively and dynamically with QA/CSV/Operations teamsEducation, experience and technical skills:• Degree in a Scientific discipline• Minimum of 3-5 years of experience in Pharmaceutical, Biotech, or Medical Devices• Familiarity with related GMP/GCP/GLP procedures and requirements.• Knowledge of appropriate Quality Systems and cGMP requirements (FDA, EU, ICH) with the ability to assess compliance risks• Proven track record in Quality Assurance with a focus on document audits• Experience within Quality Control or GCP/GLP testing facilities would be a distinct advantage• General exposure and experience in a GMP/Validation discipline with a knowledge and understanding of pharmaceutical laboratory environment would be a distinct advantageIf you meet the above criteria for the Quality Assurance Advisor role we would love to hear from you. Upload your CV for immediate consideration and please be assured that your CV will be treated with the strictest of confidence and not sent anywhere without your consent. For more information please contact Alex Barratt on .Reed Technology are an equal opportunities employer that are operating as a recruitment agency.