Training Manager

About the role

As a global medtech company, we are driven by our Vision of changing the trajectory of lives for a new day and our Mission to create ingenious solutions that ignite patient turnarounds. Our relentless commitment to patients and strong legacy of innovation in healthcare are the foundation of our future. If you're looking for a new chance, a new beginning, a new trajectory, LivaNova is where your talent can truly thrive. Join our talented team members worldwide to become a pioneer of tomorrow—because at LivaNova, we don’t just treat conditions — we aspire to alter the course of lives.

Responsibilities

• Training Strategy & Program Management: Develop and execute the site's manufacturing training and development strategy aligned with business objectives, growth plans, quality requirements, and operational needs. Establish and maintain a comprehensive training framework for production associates, technicians, engineers, supervisors, and support functions.
• Skills Matrix & Workforce Capability Management: Develop, implement, and maintain site-wide skills matrices for all manufacturing roles. Establish standards for proficiency levels, certification requirements, and requalification criteria.
• Training Content Development: Design and develop engaging training materials utilizing adult learning principles. Create training curricula, presentations, e-learning modules, practical exercises, qualification checklists, and knowledge assessments.
• Qualification & Competency Management: Establish and maintain standardized qualification processes for manufacturing processes, equipment, and critical operations. Implement methods to assess knowledge, practical skills, and operator proficiency.

Requirements

• Bachelor's degree in Education, Organizational Development, Engineering, Manufacturing, Business, Life Sciences, or a related field.
• 3+ years developing training systems, competency programs, and workforce development initiatives.
• Experience supporting medical device, pharmaceutical, biotech, aerospace, or similarly regulated manufacturing organizations.
• Experience creating and managing skills matrices, qualification systems, and onboarding programs.
• Strong project management and change management skills.
• Demonstrated ability to influence and collaborate across multiple functions.

Qualifications

• Experience in medical device manufacturing.
• Knowledge of FDA Quality System Regulations, ISO 13485, GMP, and Good Documentation Practices.
• Experience implementing Learning Management Systems (LMS).
• Experience supporting high-mix, low-volume or high-complexity manufacturing environments.
• Professional certifications in training, instructional design, lean manufacturing, or quality systems.

Pay

A reasonable estimate of the annual base salary for this position is $95,000 - $125,000 + discretionary annual bonus.