BOEHRINGER INGELHEIM VETMEDICA, INC. Team Leader/Group Leader, QA Release in ST. JOSEPH, Missouri

Boehringer Ingelheim is an equal opportunity global employer who takes pride in maintaining a diverse and inclusive culture. We embrace diversity of perspectives and strive for an inclusive environment which benefits our employees, patients and communities.Team Leader/Group Leader, QA Release-1810522Description:The basic purpose of this position is to provide technical direction and supervision in the QA Release department according to company policies and corporate business plans, to provide technical competence through proper selection and training the work force, assure QA Release functions are performed according to current regulatory requirements and company policies, maintains area of responsibility within budget guidelines and serves as a backup to the Associate Director, QA Release or direct supervisor in the event of their absence.As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies' success. We realize that our strength and competitive advantage lie with our people. We support our employees in a number of ways to foster a healthy working environment, meaningful work, diversity and inclusion, mobility, networking and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim's high regard for our employees.Duties and ResponsibilitiesDocumentation Review/Approvals:Resolves major issues that are not defined by SOP.Performs review and approvals of MBPS/CBRs/international permits for international releases.Performs documentation review of media fills and media fill protocol approvals as needed.Change Control:Performs review and approvals of change controls as a subject matter expert (SME) in QA Release for routine change controls.Performs review and approvals of significant change controls (new facility/new equipment/new product).Completes change control action items as assigned.Revises existing procedures as changes occur.Creates new documents (SOPs/Forms/templates) as needed.Deviations/CAPA:Initiates deviations in Quality electronic systems when non-conformances are detected during documentation review.Assesses reviews and approves deviations (dept approver) and assigns investigations as needed.Writes or participates in deviation investigations for determination of appropriate root causes.Serves as QA approver for investigations as needed.Performs follow-up on CAPAs for completion for self as well as direct reports. Ensures CAPA extensions are requested prior to due dates as needed.SAP:Performs movement transactions in SAP system of product as needed.Performs usage decisions for batch release in SAPPerforms second check in SAP prior to batch release.Performs conditional usage approvals as needed.Serves as a key user for SAP in the resolution of system or set up issues.Performs assessment and approvals of requests for items that are returned to stock.Projects:Actively participates on project teams as assigned by supervisorCoordinates and leads projects within group without supervision.Coordinates and leads projects including other departments/groups.Serves as department SME on cross functional groups.Training:Completes all assigned training by target due dates as assigned by BIVI.Completes on the job training for each assigned job task.Cross trains on other job tasks within department.Assists with training other individuals within the department on specific tasks.Performs training other individuals within department per assigned training plans.Assists QA management with the development of training plans within department and trains others.Develops training plans and trains others, including training outside of area of responsibility.Develops and maintains training curricula within areas of responsibility.Regulator