Manufacturing Training Lead - GMP & Compliance

ThermoFisher Scientific

Vilvoorde

Sur place

EUR 38 000 - 48 000

Plein temps

14 jours+

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Résumé du poste

Thermo Fisher Scientific in Vilvoorde, Belgium, is seeking a Training Coordinator to design and maintain comprehensive training programs for manufacturing operations. You will ensure employees have the knowledge and skills to meet quality and compliance standards, while coordinating training initiatives and creating engaging content.

You will collaborate with cross‑functional teams, track program effectiveness, and support regulatory audits, maintaining high standards of documentation and

Qualifications

  • 4+ years of experience in training/coordinator roles.
  • Experience developing and delivering training programs and materials.
  • Proficiency in LMS and training documentation systems.
  • Advanced skills in Microsoft PowerPoint and Excel.
  • Ability to collaborate across departments and manage multiple priorities.

Responsabilités

  • Develop and maintain comprehensive training programs for manufacturing operations.
  • Ensure employees are equipped with knowledge and skills to maintain quality and compliance.
  • Coordinate training initiatives, develop engaging content, and track effectiveness.
  • Support regulatory audits and inspections and maintain training documentation.

Connaissances

Training program development
LMS experience
PowerPoint
Excel
Documentation accuracy
Cross-functional collaboration

Formation

High/Secondary school diploma or equivalent

Outils

LMS software
MS Office (PowerPoint, Excel)

Description du poste

Thermo Fisher Scientific in Vilvoorde, Belgium, is seeking a Training Coordinator to design and maintain comprehensive training programs for manufacturing operations. You will ensure employees have the knowledge and skills to meet quality and compliance standards, while coordinating training initiatives and creating engaging content.

You will collaborate with cross‑functional teams, track program effectiveness, and support regulatory audits, maintaining high standards of documentation and

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