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Grifols Shared Services North America, Inc Process and reliability Engineer in Dublin, Ireland

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.

The role involves developing, implementing, and optimizing manufacturing and packaging processes, providing technical support to the teams, driving continuous improvement initiatives, ensuring compliance with regulatory and internal guidelines, collaborating with cross-functional teams, and preparing and maintaining necessary technical documentation. This position requires a strong knowledge of pharmaceutical manufacturing and packaging processes and experience in GMP environments, excellent problem-solving and analytical skills, and the ability to work well in a team. A significant part of the role involves project management, ensuring that all projects are delivered on time, within scope.

KEY RESPONSIBILITIES

  • Identify and analyse opportunities for product quality, process and efficiency improvement, implementing corrective actions as necessary ensuring compliance with relevant procedures and Good Manufacturing Practices (GMP).

  • Conduct and oversee trials, ensuring proper execution and documentation in accordance with company standards.

  • Provide hands-on technical support to the teams, ensuring optimal performance.

  • Collaborate with internal departments and vendors to troubleshoot and resolve repetitive issues in a timely and efficient manner

  • Engage with internal and external stakeholders on new equipment acquisition and projects, managing these initiatives from inception to completion.

  • Work with the Grifols Engineering team on the design, installation, and validation of new equipment, ensuring alignment with company standards and objectives

  • Utilize continuous improvement methodologies to enhance process efficiency and effectiveness.

  • Monitor and analyse process performance metrics, making necessary adjustments to optimize production.

  • Collaborate with Quality Assurance and Operations departments to ensure product quality and consistency.

  • Conduct initial training sessions on process improvements and new procedures as required to the relevant training team.

  • Work closely with the relevant department as required, fostering a collaborative work environment.

  • Prepare and present written reports and presentations as required, communicating key information to relevant parties.

PERSON SPECIFICATION

  • Must be proactive, results oriented, and have strong attention to detail.

  • Self-starter with strong work ethic and the ability to exercise good judgment.

  • Ability to effectively prioritize and manage multiple tasks to meet targeted deadlines.

  • Strong interpersonal skills with the ability to interact with personnel at all levels in a team environment.

  • Excellent verbal and written communication skills in the English language.

Desirable:

  • Experience in pharmaceutical manufacturing and packaging processes

  • Knowledge of serialization systems

  • Experience with vision systems

  • Experience in optimization of processes with a result of increased efficiency.

  • Data analysis knowledge to identify trends and improvements

  • Participation on different stages of machinery acquisition: FAT, SAT, commissioning and qualification.

  • Knowledge in automation and mechatronics

Qualifications

  • Minimum Bachelor's degree. Emphasis on Biology, Chemistry, Pharmacy, Chemical Engineering, Mechatronics, Mechanical Engineering or closely related scientific / technical discipline is preferred.

  • Minimum of 1-3 years of related experience in a pharmaceutical, GMP, or EU regulated environment is required.

Our Benefits Include:

  • Highly competitive salary

  • Group pension scheme - Contribution rates are 5% employer and 5% employee

  • 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. Golf, 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

#LI-FD1

Locatin: Grange Castle International Business Park, Grange, Clondalkin, Co. Dublin, D22 K2R3 (https://www.google.com/maps/place//data=!4m2!3m1!1s0x486773bd46855f9f:0xbe0e9ad7159de122?sa=X&ved=2ahUKEwjlosT9q-KEAxUeQEEAHaEGCV4Q4kB6BAgREAA)

Req ID: 523306

Type: Regular Full-Time

Job Category:

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