At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world.
Organization Overview:
Lilly has built a Next Generation Biotech Drug Substance Manufacturing Facility in Limerick, Ireland. This facility will be Lilly’s most technically advanced manufacturing site and will include next-generation manufacturing technologies and advanced data collection and analysis platforms that will deliver improvements in safety and quality, and increased productivity and process performance. This is a unique opportunity to be a part of the process automation team standing up a greenfield manufacturing site, and the successful candidate will help expand the existing organization and foster a culture of digital excellence enabling GMP manufacturing operations.
Responsibilities:
This role will require support of day-to-day operation's across the site’s campus where the Building Management System (BMS) is in use. This includes manufacturing, warehousing, central utility plant and labs. The role will involve working with Engineering and Operations personnel to trouble shoot issues, making changes to the control systems in line with site change control procedures and site standards, responding to system events and performing routine computer system maintenance checks. You will be a key member of the Utilities process team. In addition, responsibilities will include:
Providing subject matter expertise for BMS design, development, installation, testing, validation and lifecycle support.
As the BMS Custodian, you will:
Lead and oversee the work being delivered by equipment vendors and trade partners. This includes developing requirements for the system in line with industry and Lilly standards
Ensure BMS software design, coding/ configuration and testing meet standards and operational needs
Review and approve functional requirements, design specifications, network architectures, application software, panel design, graphics and test specifications.
Attend equipment and software FATs when required
Support commissioning of changes to existing or new equipment
Communicate effectively on system status and any related system performance to management
Develop standard operating procedures, work instructions and other job aids to ensure the appropriate level of documentation is in place to train on, maintain and operator the automation systems.
Manage the system and related upgrade projects.
Develop strategies to ensure the system is maintained compliantly while also meeting operational needs
Promote the use of automation to improve productivity, operational efficiency and compliance.
Adhere to Lilly corporate and site safety procedures and developing automation solutions with these in mind.
Develop a ‘network’ of corporate contacts and leverage corporate expertise when needed
Basic Requirements:
5 years working experience in Biopharma engineering, operations, or manufacturing.
Experience with:
Siemens Desigo CC application
PLC/HMI configuration (S7 1500s) , IPCs, TIA portal, WinCC and Igel technology
Industrial communication protocols such as BacNet/IP, Modbus, HART, Foundation fieldbus, OPC DA & UA, Profibus, Profinet, Ethernet/IP, RS485
Siemens Simatic Login, User Management component
Systems performing backup and restore, disaster recovery
Possess a keen technical curiosity and has demonstrated strong problem-solving skills and a desire for continuous improvement
Strong collaborative skills with an ability to work effectively in a team environment
Demonstrated ability to influence peers and business partners
Demonstrated strong written and verbal communications skills
Good written and verbal communication skills for both technical and non-technical audiences
Knowledge of GMP, regulatory requirements, computer system validation
Additional Skills/Preferences:
5+ years as an engineer in a highly automated environment supporting Building Management System in a pharmaceutical/ life science industries
Experience with:
Siemens PLCs, Octoplant
AVEVA Pi, Pi Vision and Asset framework
SQL Databases
Cyber security best practices and measures
Server/Client systems
Automation networking
Automation system administration
BMS panel design
Change Control
Instrumentation knowledge
Experience of troubleshooting automation systems and connected equipment such as air handling units, pumps and room environmental monitoring
Experience is Root Cause Analysis methodologies
Experience of developing design specifications, test protocols and executing tests
Experience of developing documents with Kneat electronic document management system
Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.
Lilly does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.
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