J3690NorthamptonshirePharmaceutical CRO/CMO Science Permanent£18,000 to £23,000 per annumFull Time17/03/2017Biochemistry – QC / Stability
Chemistry – Analytical Chemistry
Chemistry - Quality Control
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We are currently searching for a QC Analyst to join a leading pharmaceutical company based in the Northamptonshire area. As the QC Analyst, you will be responsible for the analysis of samples to support drug product development.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the QC Analyst will be varied however the key duties and responsibilities are as follows:
1. Analysing APIs, in process samples and finished products using HPLC, GC, FTIR, Dissolution, Karl-Fisher and UV-Vis, amongst others; within a GMP/ GLP environment
2. You will be reviewing protocols, deviations, change controls and reports, as well as investigating incidents out of specification results and then taking action appropriately.
3.Conduct method validation and transfer in addition to stability studies, providing technical assistance for drug product development.
To be successful in your application to this exciting opportunity as the QC Analyst we are looking to identify the following on your profile and past history:
1. A relevant degree in a Chemistry discipline, e.g. pharmaceutical chemistry
2. Experience working in a GMP/ GLP environment conducting analysis of pharmaceutical products.
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.