MES Engineer

Posted Yesterday
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Concord, NC, USA
In-Office
66K-158K Annually
Junior
Healthtech • Biotech • Pharmaceutical
The Role
Supports, develops, validates, deploys, and maintains manufacturing execution systems in a GMP pharmaceutical manufacturing environment. Translates business processes into technical solutions, manages electronic execution tickets, resolves system issues, coordinates releases and lifecycle activities, and ensures systems remain validated. Partners with business stakeholders, IT teams, third parties, and global MES teams to improve manufacturing processes, prioritize work, manage escalations, and deliver compliant digital solutions. This is an onsite role with occasional on-call work and 10%–15% travel.
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. 


The MES Engineer supports, develops and/or deploys manufacturing execution systems and equipment to fulfill business needs. Provide in-depth support for new and existing manufacturing applications, systems and equipment relying on applicants' business area knowledge and computer skills. Solves existing system problems, analyzes information designs, programs and/or implements new systems or enhancements to existing systems in accordance with company standards and guidelines.


Key objectives/deliverables: 

·         Develop application knowledge and business context

·         Be an expert and resource in the business use of Manufacturing Execution System (MES) applications

·         Accurately translate business processes, which may span multiple areas, into technical terms, and vice versa

·         Leverage knowledge and communication of/with the business to create or update electronic execution tickets

·         Build and maintain awareness and knowledge of regulatory, legal, or quality requirements impacting the business areas, and ensure that solution requirements comply

·         Assist the Global next generation MES team and third parties in the validation of the MES System during the deployment of the application in the site

·         Lead the delivery and support of digital solutions and electronic tickets from the site perspective

·         Work with the business to identify and capture new opportunities, improve processes, and optimize the value MES can provide

·         Work with the business to define changes to our manufacturing process that have an impact into our electronic tickets and make the appropriate changes

·         Manage the manufacturing area agenda and workload to ensure correct delivery and prioritization

·         Effectively influence the business to drive value and to implement the appropriate digital solutions, and challenge different levels of the organization

·         Provide status reporting and manage issue escalations

·         Produce and maintain local project and validation documentation

·         Ensure systems remain in a validated state and manage their lifecycle through releases, recapitalization, and retirement

·         Ensure the incident, problem, configuration, and change/release management are all accomplished in alignment with and understanding of business need


Basic Requirements:

  • Bachelor of Science degree in IT, Chemistry, Pharmacy, Science, Engineering, or related field
  • 2+ years of relevant work experience in information technology, engineering, business support or related areas
  • Experience working with a MES in GMP setting (e.g. PharmaSuite)
  • Ability to effectively communicate with business stakeholders and IT subject matter experts, understanding and speaking the language of both
  • Qualified applicants must be authorized to work in the United States on a full-time basis. Lilly will not provide support for or sponsor work authorization or visas for this role, including but not limited to F-1 CPT, F-1 OPT, F-1 STEM OPT, J-1, H-1B, TN, O-1, E-3, H-1B1, or L-1.

Additional Skills/Preferences:

·         Prior work experience working in pharma or other GMP setting

·         Prior experience working in information security and/or cyber security

·         Demonstrated ability to influence without authority

·         Solid knowledge of Computer System Validation process

·         Demonstrated ability to analyze, anticipate, and resolve complex issues (technical, operational, or business-related) through sound problem-solving skills

·         Effectively prioritize and escalate issues

·         Demonstrated learning agility and curiosity

·         Demonstrated ability to understand manufacturing business processes and convert into IT requirements/solutions

·         Demonstrated ability to evaluate, facilitate, and drive towards risk-based decision making

·         Desire and ability to communicate using a variety of methods in diverse forums

·         Strong account management skills, including research, listening, effective communication and presentation


Additional Information:

·         Position is located in Concord, North Carolina

·         Full time position onsite, with occasional on call.

·         10% -15% Travelling and occasional off hours and weekend work is expected


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

$66,000 - $158,400

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

  • Bachelor of Science degree in IT, Chemistry, Pharmacy, Science, Engineering, or a related field
  • 2 or more years of relevant experience in information technology, engineering, business support, or related areas
  • Experience working with a manufacturing execution system in a GMP setting, such as PharmaSuite
  • Ability to communicate effectively with business stakeholders and IT subject matter experts
  • Authorization to work full-time in the United States without employer sponsorship or visa support
  • Prior experience working in pharmaceutical or another GMP setting
  • Prior experience in information security or cybersecurity
  • Knowledge of computer system validation processes
  • Ability to influence without authority and drive risk-based decision-making
  • Strong problem-solving, prioritization, escalation, learning agility, and communication skills
  • Ability to understand manufacturing processes and translate them into IT requirements and solutions
  • Strong account management skills, including research, listening, communication, and presentation

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.

Eli Lilly and Company Insights

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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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