Sterling Engineering Ltd - Ireland & Europe logo

Senior Manufacturing Supervisor

Sterling Engineering Ltd - Ireland & Europe
Department:Manufacturing
Type:ON-SITE
Region:Galway
Location:Galway, County Galway, Ireland
Experience:Mid-Senior level
Estimated Salary:€55,000 - €75,000
Skills:
GMPISO 13485FDA REGULATIONSLEAN MANUFACTURINGSIX SIGMAERP SYSTEMSSAPORACLEIFSMEDICAL DEVICESMANUFACTURING SUPERVISIONPRODUCTION PLANNINGCONTINUOUS IMPROVEMENTKPISNEW PRODUCT INTRODUCTIONAUDITSTEAM LEADERSHIP
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Job Description

Posted on: April 3, 2026

Senior Manufacturing Supervisor – Medical Devices

About the Role

We are currently recruiting on behalf of our client for an experienced Senior Manufacturing Supervisor to lead operations within a regulated medical device environment.

This is a key leadership role responsible for driving production performance, ensuring regulatory compliance, and developing high-performing teams in a fast-paced manufacturing setting.

Key Responsibilities

  • Lead daily manufacturing operations to achieve targets across safety, quality, delivery, and cost
  • Supervise and develop production teams including supervisors, team leads, trainers, and operators
  • Coordinate production planning to meet customer demand
  • Ensure full compliance with GMP, ISO 13485, and FDA regulations
  • Partner with Engineering, Quality, and Supply Chain to resolve issues and improve processes
  • Drive continuous improvement initiatives using Lean and Six Sigma methodologies
  • Monitor KPIs and implement corrective actions where required
  • Support new product introductions (NPI) and technology transfers
  • Maintain accurate documentation and ensure product traceability
  • Lead internal and external audits related to production
  • Manage staffing levels and resource planning based on demand
  • Conduct regular Gemba walks to ensure adherence to Health & Safety, Quality, and operational standards

Requirements

  • Bachelor’s degree in Engineering, Manufacturing, or a related discipline
  • 5+ years’ experience in a medical device or highly regulated manufacturing environment
  • Strong knowledge of GMP, ISO 13485, and FDA requirements
  • Proven leadership experience with the ability to develop and motivate teams
  • Experience with Lean Manufacturing, Six Sigma, or continuous improvement tools
  • Excellent communication, problem-solving, and organisational skills

Desirable

  • Experience with ERP systems such as SAP, Oracle, or IFS
  • Exposure to advanced manufacturing technologies
  • Strong interpersonal skills with the ability to influence and drive change

For a confidential conversation about the role please apply for the role or contact Owen Clancy at oclancy@sterlingengineeringeu.com By applying to this job post you agree that Sterling Engineering may process your personal data for recruitment purpose

Originally posted on LinkedIn

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