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| Job Location | Harold Hill |
| Education | Not Mentioned |
| Salary | £24,000 - £28,000 per annum |
| Industry | Not Mentioned |
| Functional Area | Not Mentioned |
| Job Type | Permanent, full-time |
A major player in pharmaceutical manufacturing is going through significant growth due to site expansion and recent FDA approvals, we are seeking QC ANALYSTs to join this busy team.This is a challenging and developing site and is the perfect opportunity for any QC Analyst to really develop their career and exposure to volume manufactured steriles - injectables - liquid product market.You will be working across all new product launches across multiple dosage forms giving you an opportunity to gain that broad experience. They are driving process improvement on site and welcome candidates that value quality, safety and efficiency to really drive the department forward.Core of your role is to perform stability sample handling including receipt, placement and retrieval into/from the stability chambers and be able to set up new stability trials according to ICH guidelines.Your responsiblities will include: - Ensure QC testing of all stability samples is performed to GMP and Data Integrity guidelines, which involves analysing samples, recording, evaluating and reporting data using approved methods.- Troubleshoot test methods and laboratory instrumentation, generating accurate test results and interpret the stability trending of own tests data to identify any significant trends and support the generation of periodic status reports for annual quality review.Successful candidates will be degree qualified (Chemistry, Analytical Chemistry, Pharmaceutical Sciences or equivalent qualification), process driven, with a keen eye for detail, excellent communication skills and the ability to follow written and oral instructions. A good understanding of Good Manufacturing Practise (GMP) and experience of working in with Pharmaceutical products or raw materials is essential.You must be able to demonstrate high levels of technical competency in a range of analytical techniques, with expertise in operation of HPLC. In addition, you will have a high degree of skill in root-cause analysis techniques, in relation to analytical, technical investigations. Plus you will have expertise in undertaking Laboratory investigations and a compliant approach to handling out of specification results.This is a great opportunity to develop your career. Feel free to contact Phil Bowers for further details and discuss the role in depth. Required skills
Keyskills :
GMP HPLC Pharmaceutical Quality Control