Sr. Specialist, Learning Management Systems Operations

Posted 21 Days Ago
Be an Early Applicant
2 Locations
In-Office
Senior level
Healthtech • Pharmaceutical • Telehealth
The Role
Administer and improve global GxP learning management systems, including ComplianceWire, training assignments, compliance reporting, data governance, integrations, security roles, and vendor relationships. Lead LMS implementations, harmonization, migrations, upgrades, testing, validation, and continuous improvement. Support audits and inspections, develop procedures and dashboards, train LMS administrators, maintain documentation, and provide technical expertise across Quality, IT, HR, and business teams.
Summary Generated by Built In

Why Us?

At Par Health, we believe great healthcare is built on getting the essentials right. We’re looking for passionate, talented individuals who share our commitment to improving lives. With a global workforce, we lead with pride and purpose—prioritizing quality and safety while fostering a culture of continuous improvement, accountability, and teamwork. Elevating the Essentials isn’t just our tagline, it’s the higher standard we live by every day.

Job Description Summary

The Senior Specialist, Learning Management Systems is responsible for the administration, maintenance, and continuous improvement of GxP learning systems and training processes. This role serves as the primary subject matter expert for learning technologies, training compliance reporting, and data governance. The position partners closely with Quality, Information Technology, Human Resources, and business stakeholders to ensure compliant and effective management of training records and learning programs. Additionally, this role plays a critical role in training system harmonization, implementation, validation, and data migration activities.

Job Description

LMS Administration & Operations

  • Serve as primary administrator and subject matter expert for Learning Management Systems (LMS) and related learning technologies for corporate and multiple sites.
  • Administer training content in the LMS and ensure training assignments align with business and compliance requirements.
  • Provide advanced user support and troubleshooting for learning systems and processes.
  • Serve as system owner delegate and technical lead for LMS configuration, vendor relationship, security roles, data architecture, integrations, reporting structures, and system lifecycle management.
  • Drive continuous improvement of learning systems and training administration processes by analyzing metrics, audit observations, system performance, and stakeholder feedback to identify opportunities to standardize, streamline, and optimize workflows, data management, and user experience.
  • Support regulatory inspections, audits, and quality assessments through preparation and retrieval of training records and documentation.

LMS Strategy, Harmonization and Continuous Improvement

  • Lead or support learning system enhancement, implementation, harmonization, migration, and continuous improvement initiatives.
  • Evaluate, coordinate, and manage vendor releases, system upgrades, integrations, and other LMS-related projects to ensure compliance, functionality, and business continuity.
  • Design and execute user acceptance testing (UAT), system testing, and validation activities for learning technologies.
  • Lead onboarding and training of LMS Administrators, ensuring consistent understanding of system functionality, processes, and best practices.
  • Develop and maintain procedures, work instructions, training materials, and system documentation related to learning systems and processes.

Other Functions

  • Assist with development/maintenance of training dashboards and program metrics.
  • Participate in cross-functional committees, project teams, and quality initiatives.
  • Assist with training communications and end-user education related to system enhancements.
  • Support learning content deployment and course maintenance activities.
  • Mentor junior team members and provide subject matter expertise on learning systems and compliance processes.
  • Support vendor management and external consultant engagements related to learning technologies.

Education & Experience

  • Bachelor’s degree or equivalent experience in Life Sciences, Quality, Information Systems, or a related field.
  • 6-8 years of experience supporting global or multi-site GxP training programs and processes.
  • Minimum of 6 years of experience with the advanced administration of ComplianceWire.
  • Demonstrated experience with computerized system validation principles and documentation.
  • Demonstrated experience with learning system harmonization, implementation, or transformation projects.
  • Experience supporting multi-site or global training programs.
  • Experience with learning analytics and dashboard development

Knowledge

  • Thorough understanding of regulatory requirements associated with change control and software validation (e.g., 21 CFR 820, 21 CFR 211, ISO 13485).
  • Understanding and knowledge of Quality Management Systems and document management systems.

Skills & Abilities

  • Technical Learning Systems Expertise
  • Data Integrity and Compliance Focus
  • Analytical Thinking, Problem Solving
  • Project Management
  • Attention to Detail
  • Collaboration and Teamwork
  • Communication Skills
  • Continuous Improvement Mindset
  • Adaptability and Change Agility

Working Conditions

  • This is a hybrid role.  Normal office conditions.  Occasional travel required.

Scope of Authority

Internal Contacts

  • Work with all sites, functions, and levels of management to assure proper assignment and documentation of all training activities.
  • Work with IT and quality validation to maintain the LMS in a validated state.

External Contacts

  • Collaborate with vendor to troubleshoot and maintain the LMS in a validated state.

Disclaimer:  The above statements are intended to describe the general nature and level of work performed by employees assigned to this job. They are not intended to be an exhaustive list of all duties, responsibilities, and qualifications.  Management reserves the right to change or modify such duties as required.

EEO Statement:

We comply with all applicable federal, state, and local laws prohibiting discrimination and harassment, and provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, gender identity, national origin, age, disability, veteran status, or genetic information, or any other classification protected by federal, state or local law. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training. 

Skills Required

  • Bachelor’s degree or equivalent experience in Life Sciences, Quality, Information Systems, or a related field
  • 6–8 years of experience supporting global or multi-site GxP training programs and processes
  • Minimum 6 years of experience with advanced administration of ComplianceWire
  • Experience with computerized system validation principles and documentation
  • Experience with learning system harmonization, implementation, or transformation projects
  • Experience supporting multi-site or global training programs
  • Experience with learning analytics and dashboard development
  • Thorough understanding of regulatory requirements for change control and software validation, including 21 CFR 820, 21 CFR 211, and ISO 13485
  • Knowledge of Quality Management Systems and document management systems

Endo Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Endo and has not been reviewed or approved by Endo.

  • Fair & Transparent Compensation Pay is considered competitive to good across many roles, with total compensation in commercial positions strengthened by sizable bonus/OTE when targets are met. Subsidiary experiences within the group also point to good compensation, reinforcing a generally positive pay story.
  • Healthcare Strength Core medical, dental, and vision coverage is strong, complemented by virtual care, disease‑management programs, and a health advocate service. Health coverage is described as good, adding perceived value beyond base pay.
  • Retirement Support A 401(k) plan provides a company match up to 4%, supporting employees’ long‑term savings. Current materials outline the matching formula clearly for prospective comparisons.

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The Company
HQ: İzmir
1,722 Employees
Year Founded: 1997

What We Do

At Endo, our far-reaching vision is simple: to help everyone we serve live their best life. As a specialty pharmaceutical company, we’re motivated by a strong sense of purpose to find better ways to meet unique medical needs. Our global team of passionate employees understands the importance of their work. We’re dedicated to supporting one another as we connect with communities and foster partnerships that elevate quality-of-life and bring the best treatments forward. Our uncompromising commitment results in the delivery of life-enhancing therapies. From intelligent product selection to commercialization, we strive to make a meaningful, tangible impact to help everyone live their best life. Endo has global headquarters in Malvern, Pennsylvania. Community Guidelines: 1. Be respectful. Everyone who visits our page should feel comfortable and respected. 2. If we see a comment that violates anything in the following list, it may be removed. • Comments that use profanity; personally attack or bully another individual; or are off-topic, misleading, factually inaccurate, political, spam, defamatory, discriminatory or promotional. • Comments that are excessively repetitive and/or disruptive to the community. • Comments that promote illegal activity, use copyrights or trademarks or are related to an ongoing legal matter. • Comments that appear to be medical advice. We reserve the right to remove a reply for any reason at any time. 3. Adverse Event Reporting: If we see a post about an adverse event, an Endo representative will need to contact you to find out more information to comply with regulatory guidelines. If you experience a side effect while using an Endo product, please consult your physician or pharmacist immediately. You may also report to the FDA at fda.gov/medwatch or 800-FDA-1088. Replies from other users do not necessarily reflect the views of Endo. We do not endorse content added by other users.

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