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Production Supervisor

Adecco
GBR
Full-time
Associate
Onsite
Discovered 4 weeks ago
GMP regulationsData integrityDeviations and CAPAsRoot cause investigationsQuality systemsPeople management

Full Job Posting

Role overview

Lead day-to-day operations in a GMP-regulated pharmaceutical production environment.

Ensure production work is safe, efficient, and compliant with quality and regulatory standards.

Lead and develop a team of production staff.

Responsibilities

  • Plan and allocate labour resources to meet production targets.
  • Manage deviations, CAPAs, root cause investigations, and quality systems.
  • Review production documentation and maintain audit-ready standards.
  • Work cross-functionally with QA, Warehouse, and Procurement teams.

Experience and skills

  • At least two years of supervisory experience in a GMP production environment.
  • Strong knowledge of GMP regulations, data integrity, and compliance standards.
  • People management skills, including coaching, performance management, and team development.
  • Understanding of Health and Safety legislation and safe working practices.
  • Problem-solving, decision-making, and continuous improvement capabilities.

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