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.
Operations Supervisor – Parenteral Formulation (Night Shift) will support start up activities for multiple suites at the RTP manufacturing site. The position will be responsible for managing two shifts on a rotating 12 hour schedule. The teams will be primarily supporting dispensing and formulation activities with supplemental support tasks for parenteral material preparation.
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 12+ direct reports (3 per shift and suite) 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 Standard Operating Procedures.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:
Additional Skills/Preferences:
Bachelor’s Degree in science, engineering, or technical fieldPrevious experience in facility/area start-up environmentsPrevious experience with Manufacturing Execution Systems and electronic batch release.Experience with root cause analysis, technical writing / authoring investigationsKnowledge of lean manufacturing principlesDemonstrated leadership experienceSkills in providing/receiving feedback and creating employee development plansBasic computer skills (desktop software) are required.Solid understanding of FDA guidelines and CGMP requirements.Excellent interpersonal, written and oral communication skillsStrong organizational skills and ability to handle and prioritize multiple requests.Strong technical aptitude and ability to train and mentor others.Ability to adjust their schedules to meet milestones and to support both teams.Ability to work in a controlled environment (classified and non-classified) which requires specific company provided gowning.Ability to wear safety equipment (safety glasses, safety shoes, protective gloves etc.)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.
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