Automation Engineering, Sr. Principal Engineer – Pharmaceutical Manufacturing - Lilly Medicine Foundry

Eli Lilly and Company; Indianapolis (IN); On-site; USD 104,000 - 174,000; Full time

Benefits offered by this job

401(k)

Pension

Vacation benefits

Medical, dental, vision

Flexible benefits

Life insurance

Time off and leave

Well-being benefits

Job summary

Eli Lilly and Company is seeking a Senior Principal Automation Engineer to lead capital projects, design reviews, and DeltaV/Rockwell automation strategies. You will mentor the process control team and drive continuous improvement while ensuring GMP compliance and 21 CFR Part 11 adherence.

Initial location at Parkwood West, Indianapolis, Indiana, with permanent placement at Lilly Medicine Foundry in Lebanon, Indiana.

Qualifications

• Bachelor of Engineering or related field.
• 8+ years in Biopharma automation engineering; 5 years at Principal Engineer level.

Responsibilities

• Lead capital project execution, design reviews and FATs.
• Mentor process control team and promote best practices.
• Ensure GMP compliance and 21 CFR Part 11 adherence.
• Develop functional requirements for control systems with Process Engineering.

Skills

DeltaV DCS

Rockwell PLC

Batch Process Automation

GMP Part 11

Education

Bachelor of Engineering

Tools

DeltaV

SCADA

MES

Job description

At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life-changing medicines, strengthen how health is understood and managed, and support the communities we serve. This is hard, urgent, selfless work—but it’s work worth doing. If you’re driven by purpose and ready to bring your best to work that truly matters for patients, we invite you to join us.

Lilly recently announced a $4.5 billion investment to create the Lilly Medicine Foundry, a new center for advanced manufacturing and drug development. The first-ever facility of its kind, combining research and manufacturing in a single location, the Medicine Foundry will allow Lilly to further develop innovative solutions to optimize manufacturing processes and increase capacity for clinical trial medicines, while also reducing costs and environmental impact.

Key Objectives/Deliverables:

• Technical Leadership - Lead capital project execution, Design, Development, commissioning & qualification and support.
• Lead and oversee the work of Site Area leads and System Integrators.
• Lead/Participate in design reviews and DeltaV application software reviews, attend equipment and software FATs.
• Develop functional requirements and process control strategies for control systems in collaboration with Process Engineering.
• Translate technical concepts for executive audience and/or non-technical stakeholders.
• Develop and implement the Automation Engineering Project Plan.
• Promote the use of Digital innovation and automation to enhance efficiency of team functions.
• Maintain validated state of the process control system application software.

Operational Excellence

• System level thinking and expertise working with multi-disciplinary teams.
• Deep Expertise working with DeltaV Distributed Control System, Rockwell Allen Bradley PLC and Batch Process Automation.
• Thorough understanding of 21CFR Part 11, GMP processes.
• Provide periodic status updates to Project Management.
• Lead/Participate in design reviews and Site system hardware reviews, attend equipment and FATs.
• Promote the use of Digital Innovation and automation to improve productivity, operational efficiency and compliance.
• Experience in clinical-stage manufacturing with flexible, multi-product capabilities is preferred.
• Thorough understanding of various process control communication protocols.
• Developing a ‘network’ of corporate contacts and leveraging corporate expertise when needed.
• Provide On-call support for operations, as needed.

Organizational Capability

• Mentor process control team to strengthen technical capabilities and adopt best practices to enhance system reliability and business continuity.
• Be a fully active member of the flow leadership in running the plant, including participation on technical sub-teams.
• Possess a keen technical curiosity and has demonstrated strong problem-solving skills and a desire for continuous improvement.
• Demonstrated initiative, good planning and organizational skills, ability to prioritize tasks, commitment to task completion and timelines.
• Demonstrated ability to influence peers and business partners, influence without authority.
• In coordination with automation and compliance consultants, set and reinforce standards for appropriate rigor in automation work products.

Basic Requirements:

• Minimum B.S. in Engineering or related degree and a minimum of 5 years (at the Principal Engineer level) and a minimum of 8+ years' experience (at the Senior Principal level) working experience in Biopharma Automation Engineering, preferably in major pharmaceutical manufacturing.
• Experience working in Biotech or Pharmaceutical manufacturing using DeltaV batch are a must.

Additional Preferences:

• Experience in design, development, commissioning and qualification of highly automated greenfield manufacturing sites utilizing SCADA, DCS, PLC and MES systems (DeltaV, Rockwell, Syncade, etc).
• Experience in facilitating and driving decision-making at an organizational level.

Other Information:

Initial location at Parkwood West, Indianapolis, Indiana. Permanent location at the new Lilly Medicine Foundry in Lebanon, Indiana.

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 is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.

Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia (AMECA), Black Employees at Lilly (BE@Lilly), Chinese Culture Network (CCN), EnAble, Evolve, Lilly Indian Network (LIN), Organization of Latinx at Lilly (OLA), Pride (LGBTQ+ Allies), Veterans Leadership Network (VLN) and Women’s Initiative for Leading at Lilly (WILL).

Actual compensation will depend on a candidate’s education, experience, skills, and geographic location. The anticipated wage for this position is $103,500 - $173,800.

Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance).

• 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)

Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly’s compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.