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Quality Systems Specialist II - Training processes and Learning Management System; LMS

Job in Mansfield, Bristol County, Massachusetts, 02048, USA
Listing for: Integrated Resources Inc.
Apprenticeship/Internship position
Listed on 2025-12-22
Job specializations:
  • Quality Assurance - QA/QC
    Data Analyst
  • Healthcare
    Data Scientist
Job Description & How to Apply Below
Position: Quality Systems Specialist II - Training processes and Learning Management System (LMS)

Quality Systems Specialist II - Training processes and Learning Management System (LMS)

Contract

Client is a Medical Device company.

Implementation of the training process and Learning Management System (LMS)

POSITION RESPONSIBILITIES:
  • Monitor and support consistent execution of Client's training process and quality training programs.
  • Support the development and implementation of Client's training procedures, LMS procedures and Client's quality training programs.
  • Support LMS administrators, strive for consistent LMS practices. Identify and communicate best practices to ensure training records are complete and accurate.
  • Consult with Client's leaders, process owner, and managers to ensure that the correct training is assigned to Client's employees.
  • Provide training records and data to support Client's Leadership and audits & inspections.
  • Develop and track Client's training metrics to monitor the process and identify improvement activities.
  • Perform other Quality System duties as assigned.
  • Perform duties in compliance with environmental, health and safety related site rules, policies or governmental regulations.
  • All other duties as assigned.
EDUCATION REQUIRED:
  • Bachelor’s Degree in a Science/Technical discipline (Quality/Regulatory) or in Training/Adult Learning Theory
  • 2+ years of experience in a quality assurance or quality control environment within a medical device, pharmaceutical or related company with Bachelors
PREFERRED QUALIFICATIONS:
  • Experience with learning management system functionality
  • Understanding of training and resources requirements within FDA regulations and ISO-13485 standards
  • Excellent oral and written communication skills
  • Ability to work in a team environment
  • Previous experience in a regulated environment

All your information will be kept confidential according to EEO guidelines.

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