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Thomas Gallagher
Life Science

+353870612325
[email protected]
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Details

Senior Production Supervisor


Reference:TG - PS - Galway Location: Galway City
Qualification:DegreeExperience:5-7 Years
Job Type:PermanentSalary: Not Disclosed
May be suitable for: Lean Team Leader, Production Engineer, Production Planner, Production Supervisor, QA Supervisor

Title: Senior Production Supervisor
Location: Ballybrit, Galway
Benefits: Top salary, bonus, pension, healthcare and 4 day week


Role:
As a Senior Supervisor will lead and manage manufacturing operations to ensure efficient production of high-quality medical devices in compliance with regulatory standards. This role involves overseeing production teams, driving continuous improvement, collaborating cross-functionally to meet business goals, and ensuring day-to-day production safety, quality, delivery, and cost targets are met.

On-site role in a cleanroom and controlled manufacturing environment.



Responsibilities:

  • Lead daily production activities, ensuring safety, quality, delivery, and cost targets are met.
  • Manage and develop production supervisors, team leads, trainers, and operators, fostering a high-performance culture.
  • Responsible for production co-ordination to meet customer demand.
  • Ensure compliance with ISO 13485, FDA, and other relevant regulatory standards.
  • Collaborate with Engineering, Quality, and Supply Chain to resolve production issues and implement process improvements.
  • Ensure that all products manufactured meet the specifications, performance & quality criteria of end users, customers, regulatory authorities, and the company.
  • Monitor KPIs and drive continuous improvement initiatives using Lean and Six Sigma methodologies.
  • Actively promote, lead, and participate in work center improvement groups and project teams, to improve quality, reduce costs, eliminate waste and improve working methods.
  • Support new product introductions and technology transfers into manufacturing.
  • Maintain accurate documentation and ensure traceability in line with GMP requirements.
  • Lead audits and inspections related to production operations.
  • Manages headcount to meet area demand in a timely manner, can validate headcount requirements in a systemic method.
  • Leads Gemba walks in their area focusing on compliance to H&S, Quality & Production standards through regular review processes and frequent line walks.


Education and Experience Requirements:
  • Bachelor’s degree in Engineering, Manufacturing, or related field.
  • 5+ years of experience in medical device or regulated manufacturing industry.
  • Strong knowledge of GMP, ISO 13485, and FDA regulations.
  • Proven leadership and team development skills.
  • Experience with Lean Manufacturing, Six Sigma, and continuous improvement tools.
  • Excellent communication, problem-solving, and organizational skills.


Does this sound like your next career move? To apply and for more info forward your application to the link provided or contact me on 087 0612325 OR [email protected]