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Training Coordinator - General

Job in West Columbia, Lexington County, South Carolina, 29172, USA
Listing for: Nephron Pharmaceuticals
Full Time position
Listed on 2026-01-12
Job specializations:
  • Quality Assurance - QA/QC
    Data Analyst
  • Healthcare
    Data Scientist
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below

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Description

Job Purpose:

The Training Coordinator – General provides administrative coordination and support for Good Manufacturing Practice (GMP) training programs. This role ensures accurate scheduling, documentation, tracking, and reporting of GMP-required training to support compliance with regulatory standards and internal quality systems. Working under the Quality & Training function, the Training Coordinator partners with Departments to maintain complete, audit-ready training records and support consistent workforce qualification.

Essential

Duties And Responsibilities Training Program Development & Delivery
  • Coordinate and support GMP training activities, including onboarding, initial qualification, certifications, requalification, and ongoing training for the departments at Nephron.
  • Schedule and track instructor‑led, on‑the‑job, and electronic GMP training to ensure timely completion and compliance.
  • Maintain accurate, complete, and audit‑ready training records in the Learning Management System (LMS) and other quality systems.
  • Ensure training documentation complies with GMP, regulatory, and internal quality requirements.
  • Coordinate with Subject Matter Experts (SMEs), supervisors, and trainers to ensure training curricula align with current SOPs, work instructions, and controlled documents.
  • Support Production and Quality teams during audits and inspections by providing training records and documentation as requested.
  • Communicate training requirements, schedules, and completion status to management.
  • Support continuous improvement initiatives related to training administration, tracking, and reporting.
On-the-Floor Training Support
  • Provide on‑the‑floor support for GMP and production training activities, including coordination of on‑the‑job training (OJT) and task qualification.
  • Verify completion of training sign‑offs and ensure accurate documentation of trainer and trainee acknowledgements.
  • Assist with training logistics on the floor, including training materials, controlled documents, and access to required systems or equipment.
  • Escalate identified training gaps, documentation issues, or GMP compliance concerns to Quality and Training leadership.
Compliance & Documentation
  • Ensure GMP training documentation is accurate, complete, and maintained in compliance with regulatory requirements, site procedures, and quality systems.
  • Support audit and inspection readiness by maintaining traceable training records and promptly providing documentation to Quality and regulatory inspectors.
  • Support investigations by providing training‑related documentation during deviation reviews and root cause analyses.
  • Monitor training completion, qualification status, and retraining requirements to ensure ongoing compliance and timely remediation of gaps.
Performance Monitoring & Reporting
  • Maintain training metrics and dashboards, including completion rates, overdue training, and certification status for departments.
Employee Development & Engagement
  • Foster a learning culture by encouraging continuous skill development, cross‑training, and professional growth across departments.
  • Establish a feedback loop by gathering insights from trainees and operational leads to improve future training sessions.
  • Provide feedback and guidance to employees during training to encourage adherence to safe practices and quality standards.
Supplemental Functions
  • Perform other training‑related duties as assigned.
Knowledge Job Specifications and Qualifications
  • Understanding of Good Manufacturing Practices (GMP) and aseptic manufacturing requirements.
  • Knowledge of training principles, adult learning techniques, and on‑the‑job training coordination.
  • Understanding of production operations, SOPs, work instructions, and process flows in a manufacturing environment.
  • Awareness of regulatory requirements applicable to production and training (e.g., FDA, EMA, ISO, Annex
    1).
  • Knowledge of training recordkeeping, reporting systems, and data integrity requirements.
Education/Experience
  • Bachelor’s degree in a relevant field (e.g., technical training, pharmaceutical sciences) preferred.
  • 1–3 years of experience in training coordination, production operations, or quality systems…
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