Senior QC Analyst

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Role Overview We are currently looking for a Senior QC Analyst to join a growing biotechnology company based in South West London. As the Senior QC Analyst you will work within the quality control department focusing on biologics in DNA and RNA establishing QC policies and processes in line with their GMP regulated environment.Duties and Responsibilities You will be responsible for analytical method development and validation of biologics processes for DNA and RNA.You will write method validation protocols.As the Senior QC Analyst you will project manage the analytical activities of products and represent the QC department on customer project teams including method transfer, qualification, validation and batch release testing as well as stability testing.Working with stakeholders in QC to create new plans, timelines, deliverables and leading the production of sample plans will be among your duties.You will support both analytical and manufacturing investigations.Experience and EducationAn MSc or BSc in a relevant scientific discipline and a number of years of industry experience working in a GMP pharmaceutical or biopharma company is essential to your application.Proven industry experience working in the QC department of a pharma or biopharma company and experience of sampling techniques, reagents preparation and analytical methods is essential for this position.Proven experience of equipment and instrument calibration, qualification and validation. To find out more about Real please visit www.realstaffing.comReal Staffing, a trading division of SThree Partnership LLP is acting as an Employment Agency in relation to this vacancy| Registered office | 1st Floor, 75 King William Street, London, EC4N 7BE, United Kingdom | Partnership Number | OC387148 England and Wales