Global Training & LMS Coordinator

Edwards Lifesciences Gruppe

Redhill (MD)

On-site

USD 39,000 - 53,000

Full time

8 days ago
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Benefits offered by this job

Competitive salary
Performance-based incentives
Benefits programs

Job summary

Edwards Lifesciences is seeking a Training Coordinator to support Global Operations & Quality. The role focuses on maintaining training records, onboarding, and ensuring compliance with ISO13485 and FDA Part 820 across the site in California.

You will manage LMS activities, assist in on-site training, and help keep certifications current while supporting Group Leaders and the training program at large.

Qualifications

  • H.S. Diploma or equivalent.
  • Good interpersonal skills, written and verbal communication required.
  • High level of self-directed initiative, organizational and recordkeeping skills, and attention to detail required.

Responsibilities

  • Process, track and maintain training and certification records in compliance to ISO13485 and FDA Part 820 regulatory requirements.
  • Receive new employees directly from New Employee Orientation (NEO) and assist in training on site-specific procedures and EH&S, as well as on global production training.
  • Ensure manufacturing training and certifications are completed within time requirements by reviewing training status of all employees in LMS.
  • Answer questions from LMS users and help them to efficiently execute their work within these systems.
  • Assist in Instructor Led Training (ILT) for general updates, in the clean room.
  • Prepare training documentation for Read and Review and On The Job (OJT) methods of training.

Skills

Interpersonal communication
Organizational skills
Attention to detail
Self-directed initiative

Education

High school diploma or equivalent

Tools

MS Word
PowerPoint
Excel
Outlook

Job description

Edwards Lifesciences is seeking a Training Coordinator to support Global Operations & Quality. The role focuses on maintaining training records, onboarding, and ensuring compliance with ISO13485 and FDA Part 820 across the site in California.

You will manage LMS activities, assist in on-site training, and help keep certifications current while supporting Group Leaders and the training program at large.

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