Lilly Jobs

Job Information

Lilly Operations Supervisor (Formulation, Day Shift) in United States

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 35,000 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.

Organization Overview:

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 35,000 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.

At Lilly, we serve an extraordinary purpose. For more than 140 years, we have worked tirelessly to discover medicines that make life better. These discoveries start in Lilly Research Laboratories, where our scientists work to create new medicines that will help solve our world’s greatest health challenges.

Lilly is designing and building a new state of the art Parenteral, Device Assembly, and Packaging Facility in Raleigh-Durham North Carolina. This is an exciting opportunity to help build a state-of-the-art facility and Quality System from the ground up.

Responsibilities:

During the project phase, the Operations Supervisor – Parenteral Formulation will support commissioning/qualification activities required to bring formulation suites into service as well as supporting site operational readiness activities. This position will require domestic travel with the opportunity for international travel based on program need. This role is expected to be an on-the-floor leader and will be a subject matter expert for the formulation process. This role will have the opportunity to be directly involved with hiring and training their team.

After project phase completion, the Operations Supervisor is responsible for shift leadership for multiple drug product formulations within the area and developing the technical expertise of manufacturing employees. This individual must ensure that the operations are adequately staffed with trained/qualified employees. Strict adherence to safety and quality rules and procedures is required. Direct line supervision for line leaders and operators on a 12 hour shift schedule (2-2-3).

Key Objectives

  • Support Site Leadership to build a diverse, inclusive, and capable site organization by delivering area operational procedures, quality processes and controls for Parenteral areas.

  • Responsible for hiring/managing 10+ direct reports working across 2 formulation suites.

  • Responsible for maintaining a safe work environment, working safely, and accountable for supporting all HSE goals.

  • Ensures adequate qualified/trained staffing for operators working on the manufacturing lines.

  • Communicate with the area Manager on quality, equipment, and operational issues and areas for improvement.

  • Responsible for the coaching, personal development, and performance evaluation of operators/technicians.

  • Originate/Investigate deviations or operational quality issues.

  • Collaborate with support functions to achieve a consensus for unexpected events during manufacturing.

  • Collaborate with support functions to update and approve Standard Operating Procedures for site start up.

  • Act as both administrator and technical leader for operations, setting a good example through demonstrated knowledge of procedures, compliance with quality systems and use of proper technique.

  • Responsible for shop floor execution as it relates to business plan, current Good Manufacturing Practice (CGMP) conformance and Operational Standards for Supply Chain Excellence (OSSCE)

Basic Requirements:

  • High School Diploma or equivalent

  • Previous experience in operations or directly supporting a pharmaceutical manufacturing operation.

  • Demonstrated leadership experience

  • Skills in providing/receiving feedback and creating employee development plans

  • Basic computer skills (desktop software) are required.

  • Solid understanding of FDA guidelines and CGMP requirements.

  • Excellent interpersonal, written and oral communication skills

  • Strong organizational skills and ability to handle and prioritize multiple requests.

  • Strong technical aptitude and ability to train and mentor others.

  • Ability to work 12 hour day shifts (2-2-3 schedule) with ability to work overtime as required.

  • Ability to work in a controlled environment (classified and non-classified) which requires specific company provided gowning.

  • Project phase will require a baseline 5 day work week with flexibility to adjust hours to support specific project tasks.

  • Ability to travel up to 100% during Asset Delivery, process training, and < 5% after startup

  • 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.

  • Completion of Post Offer Exam or Completion of Work Simulation if applicable.

Additional Skills/Preferences:

  • Bachelor’s Degree in science, engineering, or technical field

  • Previous experience in facility/area start-up environments

  • Previous experience with Manufacturing Execution Systems and electronic batch release.

  • Experience with root cause analysis, technical writing / authoring investigations

  • Knowledge of lean manufacturing principles

Additional Information:

  • The position is for the Lilly Research Triangle Park site and during the project phase will allow for a flexible working environment will the ability to periodically work remotely based on the project phase and site activities.

  • Position may require a short duration assignment of 2-6 months in Indianapolis 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 Factory Acceptance Testing of equipment.

  • Ability to wear safety equipment (safety glasses, safety shoes, protective gloves etc.)

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.

As a condition of employment with Eli Lilly and Company and its subsidiaries in the United States and Puerto Rico, you must be fully COVID-19 vaccinated and provide proof of vaccination satisfactory to the company. If you would like to request an accommodation for medical or religious reasons, you may do so at workplace_adjustment@lilly.com.

At Lilly we strive to ensure our employees are part of a team that cares about them and our shared purpose of making life better for those around the world. How do we do this? We continue to look for ways to include, innovate, accelerate and deliver while maintaining integrity, excellence and respect for people. We hope that you seek to join us on our journey as we create medicine and deliver improved outcomes for patients across the globe!

#WeAreLilly

DirectEmployers