Quality Assurance Specialist - Junior

• Posted 10 hours ago • Updated 14 minutes ago
Full Time
Part Time
Fitment

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Job Details

Skills

  • Quality Assurance
  • Instructional Design
  • Pharmaceutics
  • Biotechnology
  • Medical Devices
  • Learning Management
  • LMS Administration
  • Management
  • Reporting
  • Communication
  • Problem Solving
  • Conflict Resolution
  • LMS
  • ISO 13485
  • Quality Management
  • QMS
  • Training
  • Regulatory Compliance
  • Documentation
  • SANS
  • Auditing

Summary

Job Title: Quality Assurance Specialist - Junior

Job Location: Bridgewater, NJ

Job Duration: 6 Months



Responsibilities:

  • Support daily administration, maintenance, configuration, and operation of the ComplianceWire Learning Management System (LMS).
  • Manage LMS user profiles, user groups, training items, curricula, and training assignments.
  • Maintain quality systems training records and documentation in compliance with company policies and applicable regulatory standards.
  • Support employees and business teams with LMS administration, training assignments, and related issues.
  • Generate, download, and analyze standard, custom, scheduled, and ad hoc LMS reports.
  • Track training completion, system usage, and compliance metrics.
  • Assist with internal audits, regulatory inspections, and training documentation.
  • Identify and resolve LMS-related issues and support improvements to training processes.



Must Haves:

  • Bachelor's degree or equivalent combination of education and experience.
  • 0-1 year of experience in pharmaceutical, biotechnology, or medical device environments, preferably in quality or regulatory functions.
  • 0-1 year of Learning Management System (LMS) administration experience.
  • Ability to manage training records, assignments, user accounts, and LMS reporting.
  • Strong organizational, communication, and problem-solving skills.
  • Ability to work in a hybrid environment and coordinate with onsite training teams.



Nice to Haves:

  • Hands-on experience with ComplianceWire LMS.
  • LMS Administrator certification or equivalent demonstrated expertise.
  • Familiarity with FDA regulations, including 21 CFR 211 and 21 CFR 820, and ISO 13485.
  • Experience supporting quality management systems (QMS), training compliance, or regulated documentation.
  • Experience supporting internal audits or regulatory inspections.

Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.
  • Dice Id: 91118290
  • Position Id: Stellar - 17797-36491-1793369117
  • Posted 10 hours ago
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