Production Supervisor

Adecco; Greater London; On-site; GBP 35,000 - 45,000; Full time

Job summary

Adecco in London is seeking an experienced Production Supervisor to lead day-to-day GMP-regulated pharmaceutical production. The role requires assuring safety, efficiency, and compliance with quality and regulatory standards, while actively coaching and developing a diverse team of production staff.

You will monitor performance metrics, allocate resources, and uphold audit-ready documentation. You will collaborate across QA, Warehouse, Procurement and other functions to drive continuous

Qualifications

• Minimum 2 years' supervisory experience within a GMP production environment.

Responsibilities

• Lead day-to-day production operations in a GMP setting.
• Ensure activities are completed safely, efficiently, and in line with quality and regulatory standards.
• Coach and develop a high-performing production team.
• Plan and allocate labour to meet production targets.
• Maintain audit-ready documentation and records.

Skills

GMP regulations

Data integrity

People management

Labour planning

Health & Safety

Cross-functional communication

Continuous improvement

Audit-ready documentation

Job description

We are seeking an experienced Production Supervisor to lead day-to-day operations within a GMP-regulated pharmaceutical production environment. The successful candidate will ensure production activities are completed safely, efficiently, and in line with quality and regulatory standards while leading and developing a team of production staff.

Key Skills Required

• Strong knowledge of GMP regulations, data integrity, and compliance standards.
• Experience managing deviations, CAPAs, root cause investigations, and quality systems.
• Proven people management skills, including coaching, performance management, and team development.
• Ability to plan and allocate labour resources to meet production targets.
• Strong understanding of Health & Safety legislation and safe working practices.
• Excellent communication skills with the ability to work cross-functionally with QA, Warehouse, and Procurement teams.
• Continuous improvement mindset with strong problem-solving and decision-making abilities.
• Experience reviewing production documentation and maintaining audit-ready standards. [

Experience Required

• Minimum 2 years' supervisory experience within a GMP production environment.

This is an excellent opportunity for a hands-on supervisor looking to progress their career within a growing pharmaceutical organisation.