Lead Production Supervisor, Vascular Excellence

Abbott

Clonmel

On-site

EUR 42,000 - 62,000

Full time

14 days+

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Benefits offered by this job

Competitive salary
Advancement opportunities
Inclusive culture
Peer groups
Community impact

Job summary

Abbott Ireland Vascular Division in Clonmel is seeking a Production Supervisor to lead a manufacturing team focused on vascular devices. You will guide staffing, monitor daily operations and push continuous improvements while ensuring regulatory and Quality System compliance.

The role runs Monday–Friday with A/B shifts (days and evenings). The successful candidate will hold NFQ Level 7 qualification and 4+ years related experience in manufacturing and process improvement in a regulated

Qualifications

  • NFQ Level 7 qualification in a relevant discipline with 4+ years of related work experience.
  • Experience leading production teams and driving quality and productivity improvements.

Responsibilities

  • Lead a team of employees to improve quality and productivity.
  • Plan staffing resources and coordinate with Operations Management and Planning Schedulers.
  • Develop team through training and progressively challenging tasks.
  • Drive continuous improvement projects to reduce waste and increase efficiency.
  • Interact with Quality, Engineering, HR, Supply Chain and Finance stakeholders.
  • Maintain schedules and personnel records and ensure policy compliance.
  • Provide direction and guidance to staff and mentor junior supervisors.

Skills

Leadership
Team management
Continuous improvement
Operations planning

Education

NFQ Level 7 qualification

Job description

Abbott Ireland Vascular Division in Clonmel is seeking a Production Supervisor to lead a manufacturing team focused on vascular devices. You will guide staffing, monitor daily operations and push continuous improvements while ensuring regulatory and Quality System compliance.

The role runs Monday–Friday with A/B shifts (days and evenings). The successful candidate will hold NFQ Level 7 qualification and 4+ years related experience in manufacturing and process improvement in a regulated

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