Description
Building your career at Astellas continues to offer inspiring challenges and a chance to make your mark in doing good for others.
Our open and progressive culture is what makes us Astellas. It is a culture of doing good for others and contributing to a sustainable society.
Reporting directly to the Operations Engineering Lead, the Manufacturing Engineer is responsible for the installation, maintenance, and troubleshooting of equipment used in biologics manufacturing while ensuring compliance with regulatory standards (e.g., FDA, EMA) and Good Manufacturing Practices (GMP).
Join us in this dynamic role and contribute to our team's success at Astellas. Apply now to be part of this exciting journey.
About This Job
- Daily line technical support and troubleshooting with the Operations and Engineering Teams.
- Support implementation of effective guides and procedures for: Equipment Operation, troubleshooting etc.
- Understand and look to optimise equipment design principles.
- Provide technical training and associated documentation.
- Key technical expert in your field and in technical problem-solving practices in general.
- Implement corrective actions to address deviations and improve overall product quality.
- Collaborate with Validation Engineers to develop and execute validation protocols.
- Perform data analysis to ensure manufacturing and test readiness.
- Contribute to lean manufacturing initiatives to optimize efficiency.
- Identify areas for process improvement and implement solutions.
- Work closely with global product design teams, Quality, Operations and Engineering teams to align manufacturing processes with product development goals.
- Become process experts on Aseptic Filling and Lyophilisation.
- Participate and lead cross-functional meetings to optimal machine operation.
Essential Knowledge & Experience
- Minimum bachelor’s degree in engineering or related field or equivalent experience.
- Industry experience in Biologics/Pharmaceutical manufacturing or other relevant GMP environment.
- Understanding of biologics drug substance manufacturing processes, with a strong focus aseptic filling and lyophilization a distinct advantage.
- Excels in a fast-paced team environment and completes assigned work in timely fashion.
- Strong interpersonal skills, highly collaborative within a multi-disciplinary team and contributes to a supportive and positive work environment.
- This role is required to support GMP Operations. The work schedule is subject to change to support business operations.
Preferred Knowledge & Experience
- Direct experience in drug manufacturing
- Experience with Lean Manufacturing techniques, statistical analysis and data science techniques and implementation an advantage.
Additional information
- 20% travel (domestic and International)
- This is a permanent role.
- Based at manufacturing plant Tralee.
- This role is onsite.