Training Specialist

Pe Global

Cork

PE Global is currently recruiting for a Training Specialist for a Client site in Cork: TRAINING RESPONSIBILITIES: These include and are not limited to the following responsibilities: Formulates plan to address Site Technical Training Needs to meet Site Strategic Objectives and Department Goals and reports on progress. Design and development of Technical training to meet Site Customer needs. Tracks expenditure of Site Technical Training Budget and reports plan vs actual. Responsible for coordinating, organizing and managing consultant/training companies that support Site Technical Training Programs. Manages Site Technical Training Curricula on Compliance Wire# Manages Site Technical Training Calendar on Sharepoint. Delivers training on specialized programs. Co-ordinates Site Induction Programme. Prepares Site Training Metrics for management review. Developing systems to monitor quality of training and adherence to metrics and to implement continuous improvement strategies. Adheres to Site Training Procedures. Proactively collaborates with Site Teams on Training Best Practice and Customer needs. Participates in regulatory audits and ensure audit readiness at all times. Key Member of Site Teams to support training development requirements of Site Projects and New Product Introduction. GENERAL SCOPE OF RESPONSIBILITIES: Carry out all activities in compliance with Site procedures corporate and cGMP/EHS regulatory requirements. Commit to and demonstrate safe behaviour in every activity. Report deviations promptly to the Manager to ensure compliance with EHS and GMP requirements. Support the Site in ensuring that training standards in Operations facility are maintained to a very high standard of GMP readiness. Support investigation and resolution of Training Issues on site. Participate in Cross-Functional teams as necessary. Travel to other external sites for training as required. Carry out routine and non-routine tasks delegated by Manager according to appropriate procedures, values and standards. REQUIREMENTS: Third level qualification in science, engineering, business information systems or other relevant discipline. Knowledge of FDA/EMEA regulatory requirements. Knowledge of cGMP and GDP. DESIRABLE: Operations, quality, or training experience within a GMP regulated environment. Operations, quality, or training experience within a Life Sciences or Biopharmaceutical environment. Experience of Microsoft Word, Excel and Outlook. Experience of Business Information Systems such as Documentation Management Systems and Learning Management Systems (eg Compliance Wire), Experience of Process Improvement. Interested candidates should send their CV to Audrey.brennan@peglobal.net or call 0214297900. This job originally appeared on RecruitIreland.com.

2644 days ago