Sr Coordinator Lms Instructional Design

Johnson & Johnson

Danvers, Massachusetts, United States of America
Base: $94,350.00 - $127,650.00; bonus: eligible fo...
Not specified, likely hybrid or onsite.
4-5 years related work experience
3+ years quality assurance in regulated industry
Knowledge of qsr/gmp/gcp/iso regulations
Johnson & Johnson's Abiomed division is seeking a Sr Coordinator for LMS Instructional Design in Danvers, Massachusetts. The role involves managing training processes, compliance tracking, and developing instructional content within a regulated medical device environment

Job Summary

  • This role serves as the administrator of the Learning Management System (LMS) for all US sites within a regulated medical device environment.
  • The position requires developing high-impact training materials for GxP compliance while collaborating with subject-matter experts to translate complex knowledge into practical learning content.
  • Candidates will support end-to-end training processes, manage project timelines, and provide on-site audit support for internal and external inspections.

Matching Summary

Match Score: 85

Johnson & Johnson's Abiomed division is seeking a Sr Coordinator for LMS Instructional Design in Danvers, Massachusetts. The role involves managing training processes, compliance tracking, and developing instructional content within a regulated medical device environment.

Salary

Base: $94,350.00 - $127,650.00; Bonus: Eligible for annual performance bonus; Benefits: Medical, dental, vision, life insurance, 401(k), vacation, sick time

Skills & Requirements

Must-have

  • 4-5 years related work experience
  • 3+ years Quality Assurance in regulated industry
  • Knowledge of QSR/GMP/GCP/ISO regulations
  • Proficiency with Microsoft Office software
  • Experience with Learning Management Systems

Nice-to-have

  • Experience with ComplianceWire LMS
  • Digital learning technologies expertise
  • Critical thinking and process improvement
  • Ability to influence cross-functional teams
  • Strong written and verbal communication skills

Key Requirements

  • Bachelor's degree required; Scientific or Engineering discipline preferred
  • Minimum 4-5 years of related work experience
  • 3+ years of experience in Quality Assurance within Medical Device or Pharmaceutical industries
  • Working knowledge of 21 CFR Part 820 & 806, ISO 13485, and ISO 14971

Work Rights

Not specified

Tailored Resume

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