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QC AnalystRef: TJB109

Salary:£20000 - £26000 per annum

Added:29 Jun 2020

Region: South East

Sector: Pharmaceutical

Sub Sector: Quality Assurance

An excellent opportunity has arisen for a QC Analyst to join a growing organization based in Maidenhead, Berkshire. Responsibilities *Execute Quality Control analysis on Incoming Materials, Components and Products (including stability and other samples) alongside data in support of the onsite manufacturing and QC functions *Assist in making sure that QC functions operate in a fully current GMP compliant manner and in compliance with the filed regulatory dossiers for the products supported. *Participating in the writing, reviewing and implementing of SOP's, methods, protocols and reports as required. *You must be able to follow and understand specifications for sample analysis. *The successful candidate will need to be able to provide technical support/advice for QC testing whilst ensuring that the test methods are followed correctly. *Assisting with documentation, laboratory systems and processes to include updating existing ones as required. *The successful candidate will be involved in a range of audits as and when required. *You will need experience in identifying out of specification as well as atypical results and trends. *The successful candidate will always seek best practice process and should share this to all relevant stakeholders. *You will be expected to make sure all housekeeping and work safety operations within the QC laboratory take place in the correct way *Any other task given to you by relevant stakeholder in order for you to be able to perform your role Required Skills: *Degree in Chemistry, Pharmaceutical Science, analytical or related *Proven experience of 2-4 years as QC Analyst. *Strong hands-on experience of undertaking testing, analysis and development using instrumentational analysis such as: - HPLC - GC - Dissolution - UV - FTIR in a cGMP environment. *Good knowledge of GMP, ICH guidelines, BP/EP/USP methods with an understanding of QA processes and methodologies. *Experience of LIMS or equivalent system is desirable. *Sound understanding of MHRA guidelines *Good understanding of FDA guidelines and other governing bodies is desirable but not essential Additional Experience: *Strong Microsoft Office Suite experience. *Attention to detail and quality of documentation *Good interpersonal skills *Effective oral and written communication skills *Excellent organizational and planning skills *Ability to work independently *Ability to interpret data *Ability to demonstrate calm objectivity in a pressurised, results driven environment, whilst successfully dealing with often changing and conflicting priorities. For further details, please contact Tim Barratt on +44(0)1727 817 626 or email tbarratt@keypeople.co.uk

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