LMS Training Specialist

Insight Global is seeking a Quality Systems Training Specialist to support our Medical Device client. This consultant will sit remotely or onsite at the clients facility in Danvers, MA. Day to day will consist of the following:

-Administer and maintain the Learning Management System (LMS) to ensure accurate training records across the business
-Act as training coordinator for change requests when required.
-Manage and resolve training system tickets in a timely manner.
-Provide end-to-end process support by collaborating with users to ensure successful completion of training assignments.
-Generate and deliver reports for internal and external inspections and audits.
-Communicate and escalate issues to the next management level as needed.
-Execute additional activities as directed by the Training Leader to support remediation efforts.

Compensation:
$25-30/hr

Exact compensation may vary based on several factors, including skills, experience, and education

We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.

-4+ years experience administering LMS platforms (e.g., ComplianceWire, Cornerstone, or similar).
-Strong understanding of Quality Systems and FDA regulatory requirements.
-Ability to manage training workflows and documentation in a regulated environment.
-Excellent attention to detail, organizational skills, and ability to meet strict deadlines.
-Proficiency in Microsoft Office Suite (Excel, Word, PowerPoint).

-Prior experience in medical device or pharmaceutical industry.
-Familiarity with Windchill or other document management systems.
-Experience supporting audit remediation projects (FDA, EU MDR, etc.).
-Knowledge of Good Documentation Practices (GDP).

Benefit packages for this role will start on the 1st day of employment and include medical, dental, and vision insurance, as well as HSA, FSA, and DCFSA account options, and 401k retirement account access with employer matching. Employees in this role are also entitled to paid sick leave and/or other paid time off as provided by applicable law.