Dose Formulations Supervisor -Lab Supervisor

<h2>Job Overview:</h2><p style="margin: 0px;"><span style="font-family: arial, helvetica, sans-serif;"><strong><span style="font-size: 12pt; color: black;">Dose Formulations Supervisor Madison, WI</span></strong></span></p><p style="margin: 0px;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif; color: black;"> </span></p><p style="margin: 0px;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Get ready to redefine what’s possible and discover your extraordinary potential at Labcorp Drug Development<strong>.</strong> Here, you’ll have the opportunity to personally advance healthcare and make a difference in peoples’ lives with your bold ideas and unique point of view. With the support of exceptional people from across the globe and an energized purpose, you’ll be empowered to own your career journey with mentoring, training and personalized development planning.</span></p><p style="margin: 0px;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;"> </span></p><p style="margin: 0px;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">In this role you will supervisor a team of laboratory technicians that prepare test material formulations, collect and document study data, aid in study management, in addition to scheduling study work in coordination with other groups and departments. Duties include but not limited to;</span></p><p style="margin: 0px;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;"> </span></p><ul><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Manages and provides technical guidance the day-to-day formulations operations of the laboratory; arrange for adequate staffing at all times; monitor daily operations to ensure all SOP’s are being followed</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Work with scientific staff, study directors and clients to research formulation requirements for nonstandard test article preparations.</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Provides expertise and guidance for the company’s formulations needs. Requires the ability to perform dose calculations and unit conversions</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Recommends modifications in formulation methods or procedures. </span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Able to adapt techniques to new procedures or particular needs as directed.</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Supports the continuation of training of technicians (i. e., lead technician duties, use of equipment, standard formulations procedures).</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Identifies areas of improvement to maximize data quality as well as the efficiency of the personnel and laboratory areas.</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Identifies and take appropriate action with problems, potential problems with protocols, SOPs, dose preparations, and schedules with the assistance of a more experienced Formulation Coordinator or supervisor.</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Works safely with known and unknown hazardous chemicals and maintains safe work environment.</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Assists in the implementation of novel mixing procedures and equipment</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Must be comfortable working in an Animal Research Environment and be flexibile with start times</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Experience in project management</span></li></ul><p style="margin: 0px;"> </p><p style="margin: 0px;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;"><span style="font-size: 8pt; font-family: Arial, sans-serif; color: #000000;">#LI-DZ1</span></span></p><h2>Education/Qualifications:</h2><ul><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">BA/BA degree in Life Sciences (Biology, Chemistry, Biochemistry or related field)</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Experience in dose formulation may be substituted for education.</span></li></ul><h2>Experience:</h2><ul><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">3 years' of experience in related professional roles required.</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Prior supervisory in a laboratory or research setting preferred.</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Knowledge of GLPs (Good Laboratory Practices) and regulatory agency guidelines (e. g. FDA, EPA, etc.).</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Prior experience in preclinical research studies preferred but not required </span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Prior experience in client relations and management of a budget highly preferred.</span></li></ul>