Production Manager

September Consulting Ltd; Dublin; On-site; EUR 70,000 - 90,000; Full time

Job summary

September Consulting Ltd is seeking a Production Manager in Dublin to lead high-volume assembly and packaging operations. The ideal candidate will have 5+ years of production management experience in a regulated manufacturing environment, focusing on manufacturing excellence, compliance, and continuous improvement. This role involves leading teams, ensuring quality standards, and driving a Safety-First culture, making it a fantastic opportunity to join a respected manufacturer in the medical device sector.

Qualifications

• 5+ years’ experience in a production management or supervisory role in a high-volume manufacturing environment.
• Experience working in a regulated industry (medical devices, pharma, or similar).
• Strong documentation and IT skills; knowledge of budgetary control is a plus.

Responsibilities

• Lead Shift Managers and production teams to deliver daily performance targets (SQDCP).
• Ensure full compliance with quality, regulatory, and environmental standards.
• Coach, mentor, and develop your team through regular reviews, training plans, and project ownership.

Skills

Manufacturing excellence

Compliance

Continuous improvement

People management

Problem solving

Education

Third-level qualification in Engineering, Manufacturing, or Science

Job description

We’re currently recruiting for a Production Manager to lead high-volume assembly and packaging operations within a regulated manufacturing environment in Dublin. This is an exciting opportunity for an experienced people leader with a strong background in manufacturing excellence, compliance, and continuous improvement.

You’ll play a key role in driving performance across Safety, Quality, Delivery, Cost, and People (SQDCP), while managing and developing cross‑functional teams across production, engineering, and quality.

The Role:

• Lead Shift Managers and production teams to deliver daily performance targets (SQDCP)
• Build and champion a Safety‑First culture across the site
• Ensure full compliance with quality, regulatory, and environmental standards
• Optimise resource planning to ensure smooth, efficient manufacturing flow
• Monitor and manage stock levels of WIP and finished goods
• Take a lead role in internal and external audits
• Support and drive a continuous improvement agenda, in partnership with CI and automation teams
• Coach, mentor, and develop your team through regular reviews, training plans, and project ownership
• Lead the weekly BOS (Business Operating System) meetings to support productivity and OEE targets
• Support site‑wide improvement initiatives and cross‑functional projects

What We’re Looking For:

• A third‑level qualification in Engineering, Manufacturing, or Science
• 5+ years’ experience in a production management or supervisory role in a high‑volume manufacturing environment
• Experience working in a regulated industry (medical devices, pharma, or similar)
• Proven knowledge of production principles, manufacturing operations, and compliance standards
• Strong people management and team development skills
• Proactive mindset with a hands‑on approach to problem solving
• Comfortable working cross‑functionally across Engineering, Maintenance, Quality, and Supply Chain
• Strong documentation and IT skills; knowledge of budgetary control is a plus

Why Apply?

This is a fantastic opportunity to join a well‑established manufacturer with a strong footprint in the medical device sector. You’ll work with passionate, skilled professionals and be part of a culture that values collaboration, innovation, and continuous growth.