Began working on a 1 year contract in June 2006 with CPL solutions as a QC Analytical support analyst and was made a permanent member of the Wyeth staff in September 2006. Became the senior lab analyst in 2008. Changed role in November 2009 to QC Sample Management analyst.Job title: QC Analytical Support Analyst/QC Sample management analystMy responsibilities include• Preparation of solutions and media for the various QC laboratories. • Sterilization of solutions, equipment… Show more Began working on a 1 year contract in June 2006 with CPL solutions as a QC Analytical support analyst and was made a permanent member of the Wyeth staff in September 2006. Became the senior lab analyst in 2008. Changed role in November 2009 to QC Sample Management analyst.Job title: QC Analytical Support Analyst/QC Sample management analystMy responsibilities include• Preparation of solutions and media for the various QC laboratories. • Sterilization of solutions, equipment and bio-hazardous waste for the QC laboratories using Fedegari/Steris Autoclaves. • Calibration and use of laboratory instrumentation.• Designated point of contact for maintenance/calibration issues for all laboratory instrumentation in the solution prep labs. • To perform sample login, review of tests, samples and reagents and instrument calibration activities using LIMS• Maintaining a cGMP environment through performing SOP’s. • The Review, Approval, Request, Issue, Control and archiving of Logbooks.• The creation of On the Job Training Qualification Forms, training outlines and course content development.• Reporting any non-conformances to the QC Supervisor • Preparation and review of area documentation. . • Training/Mentoring of other analysts.• Archival & Retrieval Requests of cGMP Documentation• Perform Safety and GMP Audits as per schedule• Routine water sampling across all areas of the site.• Receipt and manipulation of in process and final stage products for QC testing.• Responsible for sample shipments to and from the site.• Implementing the sites 6S/Lean programme in the solution prep lab.• Performing and assisting in additional duties as may be directed by the QC Supervisor Analytical Support Show less

Worked as a Clinical data coordinator for six months. Core responsibilities included screening medical trial data and correction of any errors discovered in electronic copies.