Associate Director - Engineering (Automation)

Posted 23 Days Ago
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Houston, TX, USA
In-Office
123K-180K Annually
Senior level
Healthtech • Biotech • Pharmaceutical
The Role
Lead and supervise the process control engineering team for a greenfield API manufacturing site, supporting project delivery, startup, and GMP operations. Hire and develop staff; define automation standards, SOPs, and control strategies; collaborate with project teams, system integrators, and regulators; manage budgets, performance metrics, compliance, and continuous improvement to ensure reliable, compliant automation systems.
Summary Generated by Built In

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. 


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 40,000 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.

Lilly is currently constructing an advanced manufacturing facility for production of API molecules located in Houston, TX. This facility is intended to provide APIs for current and future products, including new modalities. This is a unique opportunity to be a part of the site technical team for the startup of a greenfield manufacturing site, and the successful candidate will help to build the organization, the facility and the culture to enable a successful startup into GMP manufacturing operations.

The Associate Director – Engineering (Automation) is responsible for the supervision of the process control engineers and technicians that support the daily operations of the facility. The Associate Director is also responsible for the productivity and development of the employees with the purpose of ensuring that reliable and compliant control applications and systems are used in the manufacturing of API drug substances. Additionally, the Associate Director partners to influence and implement within the process control organization and across functional disciplines to support the process control technical agenda, business plan priorities, and compliance objectives.

In the project delivery phase and startup phase of the project, leadership roles will be fluid and dynamic as we endeavor to support the project delivery, build a new organization, develop and implement the necessary systems and business processes required to support GMP operations, and build the site culture. This will require significant collaboration, creativity and resilience as the site grows to a full scale GMP manufacturing through start up.

During the design and delivery of the project this role will be integrated into the corporate automation team GPACE (Global Process Automation & Control Engineering) and then transition fully to a site-based process team position.  During delivery, this role will collaborate with A&E firms, system integrators, and corporate and site engineering peers. 

Post-project delivery, this role will support GMP manufacturing operations in the central engineering function supporting one or more process teams.  This role will require significant collaboration, creativity and resilience as the site grows to a full scale GMP manufacturing site through start up. 

 

Responsibilities:

Pre-Startup and Startup Phase:

  • Attract, hire, and onboard top talent to the Process Control Engineering team, establishing the right attitude, curiosity, and learning agility to deliver on the site mission.

  • Build the organization with the necessary capability, capacity, and culture to operate this facility to the highest standards of safety, quality, and operational excellence.

  • Develop and implement the business systems and processes needed to run the site, leveraging existing Lilly knowledge where necessary, but also incorporating external experience.

  • Establish lean practices and a continuous improvement mindset throughout operations and the direct supporting organizations.

  • Support the project team to deliver the facility by providing feedback and support on design decisions, commissioning & qualification strategies, and automation-related deliverables.

  • Collaborate with the project team to ensure the right decisions are made to meet project deliverables and longer-term strategic goals for the site.

  • Organize and implement strategy for creating standard automation and process control operating procedures (SOPs) for startup and post-startup phases.

  • Plan and manage business operational expenses, capital, and headcount targets. 

 

Post-Startup:

  • Supervise and coach process control team, including completing performance reviews and development plans.

  • Staffing, including recruiting, resource planning, and succession planning.

  • Process control work coordination.

  • Review and monitor financial performance; commit to meeting targets.

  • Develop and implement the Process Control Engineering Business Plan.

  • Demonstrate a commitment to environmental, health, and safety (including PSM).

  • Identify, track, and report key indicators of functional performance.

  • Ensure team is operating in a state of compliance.

  • In coordination with automation and compliance consultants, set and reinforce standards for appropriate rigor in automation work products.

  • Assure focus by engineers and completion of critical assignments with appropriate monitoring and reporting.

  • Review and approve automation-related deviations and change controls.

  • Review and approve automation and process control standard operating procedures (SOPs).

  • Ensure technical review and approval for documents, including investigations, change controls, regulatory submissions, validations, procedures, and control strategies.

  • Interact with regulators, customers, or other outside stakeholders on business issues or in support of internal and external agency audits.

  • Network globally to share best practices, rationale, and control strategies to ensure harmonization and alignment between sites.

  • Be a fully active member of the flow leadership in running the plant, including participating on management sub-teams.

  • Develop future management and technical expert leadership for the site.

 

Basic Qualifications:

  • Minimum B.S. in Engineering (preferably Chemical Engineering)

  • 5 + years of experience in Process Control and Automation Engineering, preferably in API manufacturing.

  • 3+ years of related leadership experience

 

Additional Skills/Preferences:

  • Experience with automation platforms including Rockwell Automation and Emerson DeltaV. 

  • Ability to instill teamwork within the department and demonstrate key interpersonal skills.

  • Ability to ensure appropriate technical depth and rigor with departmental technical deliverables.

  • Successful application of organizational models through recruiting and retention of employees.

  • Ability to make decisions independently and to network with others as appropriate.

  • Ability to function in a team environment as a leader and as a member of management teams.

  • State licensure as a Professional Engineer is not required but is encouraged. 

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

$123,000 - $180,400

Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including 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; and 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.

#WeAreLilly

Skills Required

  • B.S. in Engineering (preferably Chemical Engineering)
  • 5+ years of experience in Process Control and Automation Engineering
  • Experience in API manufacturing (preferred in context of process control)
  • 3+ years of related leadership experience
  • Experience with automation platforms (Rockwell Automation, Emerson DeltaV)
  • Ability to recruit, onboard, and develop technical teams
  • Ability to ensure technical rigor and review/approve automation deliverables, validations, and change controls
  • Commitment to environmental, health, and safety (including PSM) and GMP compliance
  • Ability to interact with regulators and support audits
  • State licensure as a Professional Engineer (encouraged)

Eli Lilly and Company Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Eli Lilly and Company and has not been reviewed or approved by Eli Lilly and Company.

  • Retirement Support Feedback suggests long-term savings are bolstered by a defined-benefit pension alongside a company 401(k) match and retiree health options. These elements make total compensation feel strong beyond base salary.
  • Leave & Time Off Breadth Feedback suggests paid time off is expansive, with substantial vacation, company shutdown days, and milestone time. This breadth of leave is viewed as a meaningful part of overall rewards.
  • Parental & Family Support Feedback suggests family-building and caregiving support are robust, including paid parental leave, adoption or surrogacy assistance, and backup care. These programs enhance the perceived value of benefits across life stages.

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The Company
HQ: Indianapolis, IN
39,451 Employees
Year Founded: 1876

What We Do

Eli Lilly and Company engages in the discovery, development, manufacture, and sale of products in pharmaceutical products business segment. For more than a century, we have stayed true to a core set of values – excellence, integrity, and respect for people – that guide us in all we do: discovering medicines that meet real needs, improving the understanding and management of disease, and giving back to communities through philanthropy and volunteerism.

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