Manufacturing Supervisor - Albumin Filling

Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.

At Grifols, we believe that diversity adds value to our business, our teams, and our culture. We are committed to equal employment opportunities that foster an inclusive environment. 

Position Summary:

What You Will Do:

• Lead day-to-day albumin filling operations, ensuring production targets are achieved safely, efficiently, and in compliance with GMP requirements.
• Support the start-up, qualification, validation, and commercialisation of manufacturing processes and equipment.
• Collaborate with Quality, Engineering, Supply Chain, Validation, Regulatory Affairs, and EHS teams to support manufacturing objectives.
• Ensure products are manufactured in accordance with quality standards, HPRA, FDA, and other regulatory requirements.Monitor and drive department performance through key metrics such as OEE, production output, yield, and resource utilisation.
• Support investigations, root cause analysis, and CAPA activities to drive continuous improvement.
• Identify opportunities to improve safety, quality, efficiency, reliability, and productivity.
• Lead, coach, and develop a team of manufacturing personnel, including training, performance management, and career development.
• Maintain training programmes and ensure adherence to standard operating procedures and best practices.
• Promote a strong safety culture through incident management, audit readiness, and environmental compliance.
• Manage workforce planning, scheduling, attendance, and holiday requests.
• Ensure manufacturing documentation is completed accurately and in compliance with cGMP requirements.

What You Will Bring:

• Minimum bachelor's degree in Scientific discipline.
• Minimum 2 year's experience with leading/supervising of a team within a GMP regulated environment.
• Experience supporting facility start-up, commissioning, or new product introduction activities.
• Knowledge of EU pharmaceutical regulations and aseptic manufacturing processes.
• Train-the-Trainer qualification.
• Experience with Operational Excellence or Continuous Improvement methodologies.
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  Strong understanding of cGMP requirements and pharmaceutical manufacturing operations.
• Strong organisational, problem-solving, and decision-making abilities.
• Proactive, results-driven approach with strong attention to detail.
• Flexibility to work shifts as required.
   

Our Benefits Include:

• Highly competitive salary
• Group pension scheme - Contribution rates are (1.5% / 3%/ 5%/ 7%) and company will match
• Private Medical Insurance for the employee
• Ongoing opportunities for career development in a rapidly expanding work environment
• Succession planning and internal promotions
• Education allowance
• Wellness activities - Social activities eg. Padel, Summer Events
  
  

We understand that self-doubt can hold talented individuals back from applying for opportunities. We encourage everyone who meets the qualifications to apply – we're excited to hear from you

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Location: Grange Castle International Business Park, Grange, Co. Dublin, D22 K2R3       

Learn more about Grifols