Scientific Coordinator

<h2>Job Overview:</h2><p style="margin: 0px; text-align: justify;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;"><strong>Do you have experience working within a scientific environment?</strong></span></p><p style="margin: 0px; text-align: justify;"> </p><p style="margin: 0px; text-align: justify;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;"><strong>Do you want to work in an exciting new role for a company that will give you tailor made training and development?</strong></span></p><p style="margin-bottom: 0.0001pt; text-align: justify;"> </p><p style="margin-bottom: 0.0001pt; text-align: justify;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Labcorp Drug Development is a global, world-leading Life Sciences Contract Research Organisation that provides dedicated and fully comprehensive laboratory testing and drug development services to the pharmaceutical industry. We strive to make a difference to people’s everyday lives by bringing essential medicines to the market.  </span></p><p style="margin-bottom: 0.0001pt; text-align: justify;"> </p><p style="margin-bottom: 0.0001pt; text-align: justify;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">At Labcorp Drug Development in <strong>York</strong>, we are looking for a <strong>Scientific Coordinator</strong> to join our expanding Biopharmaceutical CMC Solutions (Chemical Manufacturing Controls) team where you would be working 50% of the time in the laboratory.</span></p><p style="margin-bottom: 0.0001pt; text-align: justify;"> </p><p style="margin-bottom: 0.0001pt; text-align: justify;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;"><strong>Job responsibilities include:</strong></span></p><ul><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt; color: #000000;">To ensure all materials (reagents, consumables, critical materials and samples) in CMC are entered, located and tracked by established deadlines and in compliance with SOPs (Standard Operating Procedures) and regulatory agency guidelines; assuring the processes is followed for all materials throughout their lifecycle</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt; color: #000000;">To Perform a variety of material coordination responsibilities in compliance with appropriate SOPs, GMP(Good Manufacturing Practice) / GLP  (Good Laboratory Practice) / GCP (Good Clinical Practice) requirements and regulatory guidelines</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt; color: #000000;">Direct responsibility for ensuring that effective and efficient coordination processes are followed for incoming and outgoing materials/samples</span></li><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif; color: #000000;">Independently resolving issues through contacting internal or external customers as appropriate</span></li><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif; color: #000000;">Assisting with client visits as appropriate</span></li><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif; color: #000000;">Incorporating peer review tasks and responsibilities into workload</span></li><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif; color: #000000;">Acting as a team representative within the Department on appropriate teams and / or committees</span></li></ul><h2>Education/Qualifications:</h2><ul><li><span style="color: #000000; font-family: arial, helvetica, sans-serif; font-size: 12pt;">Scientific experience</span></li></ul><h2>Experience:</h2><ul><li style="text-align: justify;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Demonstrable experience of working within a laboratory environment</span></li><li style="text-align: justify;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Some experience and application of sample process receipt, transfer and shipping processes would be ideal</span></li><li style="text-align: justify;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Working knowledge of a functioning LIMS</span></li><li style="text-align: justify;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Ideally some experience and application of aseptic technique</span></li><li style="text-align: justify;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Knowledge or understanding of regulations (GMP / GLP / GCP)</span></li><li style="text-align: justify;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Basic computing skills, including word processing and use of spreadsheets (e.g. Word, Excel)</span></li></ul>