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Job Type:
Full-time
Minimum USD Salary: 64,500
Maximum USD Salary: 140,800

Industry:

Company: Eli Lilly and Company

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.

Actual compensation will depend on a candidate’s education, experience, skills, and geographic location. The anticipated wage for this position is
$64,500 – $140,800

The Senior Operations Associate will report to the Formulation/Material Preparation Operations Manager. The Senior Operations Associate will be responsible for providing leadership within the area’s process team, managing projects and process improvements, acting, as a liaison between operations and multiple functional groups to support event management, change controls, etc. The Senior Operations Associate will lead investigations and drive implementation of actions associated with deviations.

The Senior Operations Associate is responsible the daily performance management of the process team. This individual must ensure a cross functional collaboration between operations, engineering, quality, supply chain, and maintenance. The Senior Operations Associate will establish and hold the process team accountable for key metrics and deliverables to ensure the process is meeting expectations and actioning improvements for the process. Strict adherence to safety and quality rules and procedures is required.

Key Objectives/Deliverables:

  • Support Site Leadership to build a capable site organization by delivering area operational procedures, quality processes and controls for the Parenteral Manufacturing areas.
  • Monitor and build a strong safety culture
  • Ensure consistency of operations across shifts through active engagement on the shop floor and through Gemba walks and Practice vs. Procedure evaluations.
  • Participates and/or lead cross functional teams in the development and implementation of strategies associated with the area for the following initiatives: Continuous Improvement, Root Cause Analysis (RCA), Failure Modes Effect Analysis (FMEA), and operational readiness.
  • Understand and influence the manufacturing control strategy for their area.
  • Lead and facilitate start up activities regarding site operational readiness for the Parenteral portion of the business.
  • Lead area tours to support business reviews and / or regulatory audits
  • Trained as a Lead Investigator
  • Act as the primary investigator for the process team deviations
  • Development and monitoring of metrics for the area
  • Aid in issue resolution, batch/product approvals, and production schedule execution.
  • Lead specific activities of the process teams.
  • Potential back-up of Manager

Requirements:

  • Bachelor of Science Degree in Engineering (Chemical, Biological, or Mechanical)
  • Experience: 2 to 5 years Operations or Manufacturing Support in Pharmaceuticals
  • Qualified candidates must be legally authorized to be employed in the United States. Lilly does not anticipate providing sponsorship for employment visa status (e.g., H-1B or TN status) for this employment position.

Preferred Attributes:

  • Previous experience in facility/area start-up environments
  • Previous experience in aseptic processing
  • Career interests in Operations Leadership
  • Certified Six Sigma Green/Black Belt
  • Direct experience in protocol generation/execution and authoring specifications related to equipment parameters
  • Responsible for maintaining a safe work environment, working safely, and accountable for supporting all HSE Goals
  • Understanding of basic requirements of regulatory agencies such as the FDA, EMEA, DEKRA, and OSHA.
  • Excellent interpersonal, written and oral communication skills
  • Ability to travel up to 100% during Asset Delivery and technical transfer. Then < 10% after site startup
  • Previous experience in operations or directly supporting aseptic operations.
  • Ability to work in a controlled environment (classified and non-classified) which requires specific company provided gowning.
  • Experience with root cause analysis, technical writing / authoring investigations
  • Knowledge of lean manufacturing principles and concepts
  • Advance computer skills are required (Data Analysis – run charts, pareto charts, pivot tables).
  • Strong organizational skills and ability to handle and prioritize multiple requests.
  • Strong technical aptitude and ability to train and mentor others.

Additional Information:

  • The position is for the Lilly Research Triangle Park site.
  • Position may require a short duration assignment of 1- 3 months in Indianapolis, IN to establish specific device knowledge, establish global contacts, and provide production support. Additionally, this position may require short (less than 1 month) international travel to support operational readiness.
  • Ability to wear safety equipment (safety glasses, safety shoes, protective gloves etc.)

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 an EEO/Affirmative Action Employer and 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.

Our employee resource groups (ERGs) offer strong support networks for their members and help our company develop talented individuals for future leadership roles. Our current groups include: Africa, Middle East, Central Asia Network, African American Network, Chinese Culture Network, Early Career Professionals, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinos at Lilly, PRIDE (LGBTQ + Allies), Veterans Leadership Network, Women’s Network, Working and Living with Disabilities. Learn more about all of our groups.

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

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