Job Description

The QMS Coordinator ensures that all Standard Operating Procedures (SOPs) are drafted and maintained in line with applicable regulatory, internal, and territorial guidelines and certifications. The job holder also coordinates GMP, SOPs, and Work Procedures training for Production and Quality staff.

This is a permanent full‑time position (40 hours). Working days are Monday to Friday, 8:00am–4:30pm (flexible); the role is hybrid.

Responsibilities

  • Ensure documentation is drafted and maintained as per approved templates, formats, and identifications in the electronic Quality Management System.
  • Support and participate in GMP documentation related continuous improvement activities.
  • Assist in Quality Assurance initiatives, internal and external audits.
  • Ensure document reviews and approvals are managed efficiently and effectively.
  • Follow and adhere to all given instructions, including work procedures, SOPs, cGMP, and Good Ph...

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