Production Supervisor - Day Shift (Castlebar)

CPL

  • Castlebar, Co Mayo
  • Permanent
  • Full-time
  • 20 days ago
Production Supervisor – Day Shift (Castlebar)Medical Device / Biopharma Manufacturing – Full-Time, PermanentDue to continued expansion, our client is seeking an experienced Production Supervisor (Day Shift) to join their rapidly growing manufacturing team in Castlebar, Co. Mayo.This role involves coordinating cleanroom-based production operations within a dynamic manufacturing environment that supports the development of single-use process systems (SUPS) used globally in the manufacture of cutting-edge and life-saving biopharmaceuticals.Key Responsibilities
  • Lead and coordinate day-to-day cleanroom production operations to achieve safety, quality, and output targets.
  • Supervise, train, coach, and develop production team members, promoting strong performance and skill growth.
  • Prepare and execute daily and weekly production plans, track progress, and proactively resolve issues to ensure delivery targets are met.
  • Ensure full compliance with Health & Safety, GMP, Quality, and Line Clearance requirements.
  • Partner with planning, engineering, quality, and supply chain teams to support smooth production flow and continuous improvement initiatives.
  • Conduct root cause analysis on production issues and implement practical, sustainable solutions.
  • Support recruitment, onboarding, and performance management in line with company policies.
  • Maintain accurate training records, KPIs, time and attendance, and other administrative metrics.
  • Coordinate routine equipment cleaning and preventive maintenance tasks.
Qualifications & Experience
  • Minimum 3 years’ experience leading a production team within a high-volume manufacturing environment (medical device, biopharma, or similar).
  • Level 7 qualification in Business, Management, Engineering, or a related technical discipline is preferred.
  • Proven people leadership skills — ability to motivate, organize, and develop a team.
  • Strong problem-solving mindset with a passion for continuous improvement.
  • Excellent communication and interpersonal abilities, capable of working cross-functionally.
  • Proficiency in MS Office and manufacturing or production systems software.
  • Ability to read and interpret technical documents, safety procedures, and production specifications.
Working EnvironmentThis role is based in an ISO Class 7 cleanroom environment. Appropriate protective garments (cleanroom suit, gloves, mask, etc.) must be worn at all times. Due to product sensitivity, only non-smokers can work in this controlled environment.Benefits
  • Permanent day-shift role with long-term career development opportunities
  • Excellent training and progression in a well-established, growing manufacturing operation
  • Competitive salary and benefits package
If you’re looking to step into a dynamic leadership role within a company that’s shaping the future of biopharma manufacturing, we’d love to hear from you.

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