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The Manufacturing Training Supervisor is responsible for participating in designing, developing, facilitating and executing training requirements for Terumo Medical Corporation's (TMC) Manufacturing teams. The objective of this training is to ensure compliance to cGMP, quality, regulatory and enterprise/corporate business requirements. At a minimum, this includes the FDA's Quality System Regulation/Current Good Manufacturing Practices (21 CFR 820) and ISO-13485:2016. In addition, the successful candidate will participate in developing and facilitating objective measures for determining the effectiveness of the training content and successful learning of training objectives. The Manufacturing Training Supervisor will work with key business SME's to develop, facilitate and maintain appropriate training for Manufacturing facility personnel. The individual in this position must be a self-starter with experience in developing new and innovative business and medical device quality systems training programs from the conceptual stage. The ideal candidate must also be able to perform primarily at a tactical level with some participation in strategic level activities. This includes developing and facilitating a training schedule, curriculum, on the job training / proficiency qualification programs, records system and process for continuous improvement. The overall business goal of the Manufacturing Training Supervisor is to support the development of a quality/business culture based upon effective compliance and continuous business improvement throughout TMC.
