Job Title

BEPC Inc. provides Specialized Engineering Solutions and IT Project Management services to Fortune 500 companies in the Life Science and Technology industries. BEPC Mexico, a division of BEPC Incorporated, provides and manages consulting services for Automotive and Medical device companies throughout Mexico and around the globe. BEPC Inc. is seeking a highly experienced Training Coordinator will be responsible for planning, organizing, and delivering training programs related to Quality Management Systems (QMS), document control, and regulatory compliance within a manufacturing or medical device environment. This role supports cross-functional teams by ensuring employees are properly trained on documentation practices, systems, and quality standards. The ideal candidate brings strong experience in document control, internal audits, and training delivery, with the ability to work collaboratively across departments and drive compliance initiatives. KEY RESPONSABILITIES:Coordinate and deliver training programs on documentation practices (GDP), QMS procedures, and record retention.Develop and maintain training materials, manuals, and documentation aligned with company standards.Provide onboarding and continuous training for employees, contractors, and suppliers.Ensure compliance with ISO 13485, MDSAP, and internal quality standards.Support document control processes, including document distribution, version control, and system access training (e.g., Arena, Agile, MasterControl).Collaborate with departments such as Engineering, Quality, Manufacturing, and Projects to identify training needs.Participate in internal and external audits, including preparation and training readiness.Track training completion, maintain accurate training records, and generate reports.Support CAPA and non-conformance processes through training and documentation improvements.Identify gaps in training effectiveness and implement continuous improvement initiatives. MAIN QUALIFICATIONS:~ Bachelor's degree in Engineering, Industrial Engineering, or related field.~5+ years of experience in training coordination, document control, or quality systems within regulated industries.~ Strong knowledge of Quality Management Systems (QMS) and documentation practices (GDP).~ Experience with electronic document management systems (EDMS) such as Arena, Agile, or MasterControl.~ Experience supporting audits (internal and external).~ Strong organizational, communication, and leadership skills.~ Ability to work independently and manage multiple priorities. PREFERRED QUALIFICATIONS:Certification as Internal Auditor (ISO 13485 / MDSAP).Experience in medical devices or regulated manufacturing environments.Experience leading teams or supervising training initiatives.Knowledge of change management processes (CRs, ECOs).