Lead automation engineering strategies and operations in medical device manufacturing. Oversee project management and compliance in a hybrid role based in Stuttgart, Germany.
About the role
- Advisor Engineer in Automation Engineering at Lilly, enhancing drug development through automation in Indiana. Mentoring teams and leading project execution for innovative manufacturing solutions.
Responsibilities
- Mentor process control team, including design, controls philosophy, implementation and commissioning
- Process control work implementation and coordination
- Review and monitor financial performance; commit to meeting targets
- Develop and implement the Automation Engineering Project Plan.
- Technically lead and oversee the work of Site Area leads and System Integrator including Functional Requirements, Design Specifications, DCS Application Software, Test Specifications.
- Lead/Participate in design reviews and DeltaV application software reviews, attend equipment and software FATs
- Lead a team of automation engineers supporting commissioning
- Provide periodic status updates to Project Management
- Devising functional requirements and process control strategies for control systems in collaboration with Process Engineering
- DCS and SCADA software design, coding/configuration and testing (sequence logic, graphics, batch software etc.)
- Perform automation engineering activities including design, tuning and troubleshooting of control loops
- Implement and support electronic systems (such as plant historians, applications and software integration) used to capture process automation related production data
- Maintain the validated state of the site control systems in line with Lilly quality standards including the development and execution of validation strategies and associated documentation
- Automation support for capital projects including new product introductions
- Promoting the use of automation to improve productivity, operational efficiency and compliance
- Developing a ‘network’ of corporate contacts and leveraging corporate expertise when needed
- In coordination with automation and compliance consultants, set and reinforce standards for appropriate rigor in automation work products.
- Demonstrated initiative, good planning and organizational skills, ability to prioritize tasks, commitment to task completion and timelines.
- Possess a keen technical curiosity and has demonstrated strong problem-solving skills and a desire for continuous improvement
- Demonstrated ability to influence peers and business partners
- Good written and verbal communication skills for both technical and non-technical audiences
Requirements
- Minimum B.S. in Engineering and experience in Automation Engineering, preferably in Hybrid manufacturing.
- 10+ years working experience in Biopharma engineering, operations, or manufacturing.
- Experience in design, development, commissioning and qualification of highly automated greenfield manufacturing sites utilizing SCADA, DCS, PLC and MES systems (DeltaV, Rockwell, Syncade, etc).
Benefits
- eligibility to participate in a company-sponsored 401(k)
- pension
- vacation benefits
- eligibility for medical, dental, vision and prescription drug benefits
- flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts)
- life insurance and death benefits
- certain time off and leave of absence benefits
- well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities)
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