Eli Lilly-posted 7 months ago
$64,500 - $140,800/Yr
Full-time • Entry Level
Concord, NH
Chemical Manufacturing

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 lifechanging 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 investing over $1 Billion to build a completely new, inspiring, and highly automated campus in Concord, North Carolina which will house warehousing & logistics, parenteral operations, medical device assembly, and packaging, QC laboratories, and support teams to produce medicines for an unmet patient need. If you ever wanted to have a direct impact on building a team's culture and on how the team operates, now is the perfect opportunity! During the project phase, the Operations Associate (OA) will support commissioning, qualification, and validation of the Device Assembly and Packaging (DAP) areas as well as lead / assist in operations readiness programs (e.g. Material procurement and definition, training programs, process excellence, continuous improvement, and capacity planning). The person in this role will be the DAP area's technical subject matter expert and will be involved in hiring and training personnel. This position will require travel domestically with the opportunity for travel internationally to collaborate and learn from sites who produce our medicines currently. Once the facility is turned over to operations, the OA role is responsible for daily performance management and support of the DAP process team. This individual must ensure cross functional collaboration between operations, engineering, quality, supply chain and maintenance to meet key metrics and deliverables for the area. Above all else, the role will lead by example with a safety first, quality always approach. As a site leader and expert at our growing site, you will have significant opportunities for growth into future leadership and technical roles.

  • Lead by example with a Safety first, Quality Always mindset.
  • Lead/conduct area deviation and corrective action discussions as a lead investigator with a crossfunctional team.
  • Present operations investigations and procedures to Regulatory Agencies and act as a Subject Matter Expert (SME) for related inspections.
  • Ensure consistency of operations across shifts through active engagement on the shop floor.
  • Lead and facilitate operations readiness activities and programs for the DAP portion of the business.
  • Participate in the development and implementation of strategies focused on Continuous Improvement, Root Cause Analysis (RCA), and Operational Standards for Supply Chain Excellence (OSSCE).
  • Understand and influence the manufacturing control strategy for their area.
  • Develop, monitor, and propose solutions to improve or meet key performance indicators (KPI) for the area.
  • Support Site Leadership to build a diverse and capable site organization.
  • Bachelor's degree in a STEM or pharmaceutical related field of study.
  • At least 2 years working within manufacturing/operations.
  • Understanding of basic requirements of regulatory agencies such as the FDA, EMEA, DEKRA, and OSHA.
  • Excellence in electronic, written, and oral communication skills.
  • Strong technical aptitude as demonstrated through previous work or educational accomplishments.
  • Experience with or understanding of working within or directly supporting pharmaceutical, food, packaging, or applicable manufacturing departments.
  • Experience with highly automated equipment (inspection, filling, device assembly, packaging, etc.).
  • Advanced computational capabilities (e.g. Data Analysis, Pareto and Control charting).
  • Technical writing such as creation of standard operating procedures, work instructions, and training documentation.
  • Experience with Facility, Equipment, Systems Startup.
  • Knowledge of Manufacturing Execution Systems and electronic batch release.
  • Familiarity with Automated Storage and Retrieval System (ASRS) Warehouses or AGVs.
  • Understanding of continuous improvement methodologies and mindset - lean, six sigma, etc.
  • Experience with documentation, deviation and change management systems.
  • 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.
  • Wellbeing benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).
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