GMP Purification Supervisor - Biotech Manufacturing Lead

Grifols

Dublin

On-site

EUR 65,000 - 90,000

Full time

2 days ago
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Benefits offered by this job

Pension
Private medical
Career development
Internal promotions
Education allowance
Wellness activities

Job summary

Grifols in Ireland seeks a Manufacturing Purification Supervisor to oversee the daily purification team in a GMP-cleanroom setting. You will lead technicians, ensure SOP and safety adherence, and drive improvements across ultrafiltration, pasteurization, and related unit operations.

Join a global healthcare leader with strong training and progression opportunities. You will coordinate with maintenance and validation, safeguard batch integrity, and maintain a clean, inspection-ready environment

Qualifications

  • Bachelor’s degree in Biotechnology, Biochemistry, Chemical Engineering, or related field
  • 3+ years in biopharmaceutical manufacturing with supervisory experience
  • Knowledge of GMP, cleanroom environments, and aseptic techniques
  • Hands-on purification equipment experience

Responsibilities

  • Supervise purification technicians and manage day-to-day operations
  • Ensure GMP, SOPs and safety protocols are followed
  • Provide training, mentoring and performance feedback
  • Oversee purification processes including ultrafiltration and pasteurization
  • Coordinate with maintenance and validation teams to ensure equipment reliability

Skills

Leadership
GMP knowledge
Cleanroom experience
Purification equipment
Regulatory inspections
Communication

Education

Biotech/Biochem/C Chemical Engineering degree
3+ years biopharma manufacturing

Tools

Ultrafiltration systems
Pasteurizers
Validation equipment

Job description

Grifols in Ireland seeks a Manufacturing Purification Supervisor to oversee the daily purification team in a GMP-cleanroom setting. You will lead technicians, ensure SOP and safety adherence, and drive improvements across ultrafiltration, pasteurization, and related unit operations.

Join a global healthcare leader with strong training and progression opportunities. You will coordinate with maintenance and validation, safeguard batch integrity, and maintain a clean, inspection-ready environment

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