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 | Bretby |
Education | Not Mentioned |
Salary | Salary negotiable |
Industry | Not Mentioned |
Functional Area | Not Mentioned |
Job Type | Permanent,full-timeB |
QC AnalystDerby, Derbyshire£19K - £24K Basic + 23 Days Holiday + Bonus COMPANYOur client is a well-established specialist pharmaceutical manufacturing business based in Derby. This GMP accredited organisation are now looking to add a Pharmaceutical QC Analyst to their team, a fantastic role enabling someone to gain experience with awide range of pharmaceutical analytical techniques and methods. This is a great business which offers considerable opportunities to grow within the company, both within the lab (Senior Analyst, Supervisor, Manager) and even long-term potentially into Quality Assurance!POSITIONAs a Pharmaceutical QC Analyst, you will be responsible for: Performing quality control testing of a variety of pharmaceutical raw materials and finished products Using a wide range of testing techniques including HPLC and UV mostly, but also AA and dissolution testing Calibrating a range of laboratory equipment Investigation of any Out of Spec/Out of Trend (OOS/OOT) results Ensuring that strict cGMP compliance is adhered to in the laboratory Completing analytical reports and other subsequent documentation.The ideal candidate for the QC Analyst role will have: A BSc in Chemistry or related subject At least 2 years of industrial experience, as a QC Analyst, ideally in a pharmaceutical or other GMP regulated organisation. Experience with HPLC is essential, with any knowledge of method development/validation being highly beneficial.You must be able to take responsibility for your own projects and demonstrate excellent interpersonal and communication skills in order to effectively communicate with colleagues at all levels.Keywords: Pharma, Pharmaceutical, Finished Products, Wet Chemistry, Bench Chemistry, Titrations, HPLC, FTIR, FT-IR, UV-Vis, GMP, QC, Quality Control, Chemist, QC Analyst, QC Chemist, Lab Analyst, Laboratory Analyst, SOPs, OOS, OOT, Out of Spec, Out of Trend.