QC Analyst - CMC

<h2>Job Overview:</h2><p style="margin: 0px;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;"><strong><span style="color: windowtext;">Do you want to be a part of the world's leading drug development company?</span></strong></span></p><p style="margin: 0px;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;"><strong><span style="color: windowtext;"> </span></strong></span></p><p style="margin: 0px;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;"><strong><span style="color: windowtext;">Are you looking for a role with training and career progression opportunities?</span></strong></span></p><p style="margin: 0px;"><span style="font-family: arial, helvetica, sans-serif; color: windowtext; font-size: 12pt;"> </span></p><p style="margin: 0px;"><span style="font-family: arial, helvetica, sans-serif; color: windowtext; font-size: 12pt;">At Labcorp Drug Development in Harrogate, North Yorkshire we are looking to recruit a number of <strong>QC Analysts</strong> with or with experience to join our expanding team.</span></p><p style="margin: 0px;"> </p><p style="margin: 0px;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">The <strong>CMC</strong> (Chemistry Manufacturing Controls) division provides end-to-end analytical solutions and testing services to ensure quality control of our clients manufactured drug products. </span></p><p style="margin: 0px;"> </p><p style="margin: 0px;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">We work with leading pharmaceutical and biotech clients to ensure that their manufactured drug product or API (Active pharmaceutical Ingredient) passes all quality testing. Once this testing is complete, it brings our clients one-step closer to successfully launching that drug product on the market; helping bring medicine to patients.</span></p><p style="margin: 0px;"><span style="font-family: arial, helvetica, sans-serif; color: windowtext; font-size: 12pt;"> </span></p><p style="margin: 0px;"><span style="font-family: arial, helvetica, sans-serif; color: windowtext; font-size: 12pt;">The<span style="background-color: #ffffff;"> QC Analyst </span>will <span style="font-size: 12.0pt;">have responsibility to work with QC Scientists and the Laboratory Systems Co-ordinator to conduct all work in compliance with applicable regulatory requirements, and specifically those regulations (GLP/GMP) specified in the study plans, protocols, or work agreements governing the work in which they are involved and being a point of contact for analysts.</span></span></p><p style="margin: 0px;"> </p><p style="margin: 0px;"><span style="font-family: arial, helvetica, sans-serif; color: windowtext; font-size: 12pt;"><span style="font-size: 12.0pt;"><span style="font-size: 12pt;"><strong><span style="color: windowtext;">Job responsibilities include:</span></strong></span></span></span></p><p style="margin: 0px;"> </p><ul><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Responsibility for the efficient completion of analytical procedures within BioPharmCMC ensuring that client deadlines are met</span></li><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Provide study supervision and operational support necessary for the performance of a wide variety of studies carried out in BioPharmCMC. </span></li><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Will supervise and participate in a wide range of analytical techniques & procedures and may be a technical point of contact for clients</span></li><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Work closely with QC Scientists to ensure studies are performed according to scientific and technical standards and in a timely and cost effective manner</span></li><li><span style="font-family: arial, helvetica, sans-serif;"><span style="font-size: 12.0pt;">Provide guidance to more junior members of staff in all aspects of laboratory work including routine assays and assistance with trouble shooting and method transfer / validation work</span><span style="font-size: 12.0pt;"> </span></span></li><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Provide appropriate procedural and technical training for BioPharmCMC staff to develop specific study capabilities</span></li><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Have full awareness of study activity and deadlines and strive to keep projects on schedule</span></li></ul><h2>Education/Qualifications:</h2><ul><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">The post holder should have a relevant scientific degree </span></li></ul><h2>Experience:</h2><ul><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Experience or knowledge of analysis such as  <strong>PCR, Gel or Capillary Electrophoresis, HPLC, Elisa, DNA extraction, LCMS, cell based assays </strong>and using <strong>aseptic techniques</strong> preferably in the pharmaceutical industry</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">An understanding of health and safety policies, Company policies and procedures, and an understanding of GxP</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">The post holder should be able to communicate effectively at all levels, with other employees, as well as external clients, suppliers, etc.</span></li></ul>