Production Supervisor – Day Shift (Castlebar) Medical Device / Biopharma Manufacturing – Full-Time, Permanent

Production Supervisor – Day Shift (Castlebar)

Medical Device / Biopharma Manufacturing – Full-Time, Permanent

Due 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 Environment

This 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.