- Roche (Indianapolis, IN)
- …schedule. You will troubleshoot equipment and process issues, lead /contribute to process improvement/characterization projects, train maintenance and production ... controls systems (PLCs, HMIs, Motion Control, etc.) **Preferences** + Familiar with GMP in a regulated environment (Medical Device or Pharmaceutical). + Previous… more
- Amcor (Evansville, IN)
- …and work well with other Laminate Extrusion Technicians, and Assistants 5. Ability to lead people in a positive manner 6. Must become fork truck certified with ... safely and accurately 7. Must become LOTO certified 8. Able to follow GMP regulations 9. Ability to readhandheldmicrometer 10. Able to stand/walk for seven hours… more
- Lilly (Indianapolis, IN)
- …develop operational readiness scope across multiple technical areas simultaneously. + Lead cross-functional project teams to develop operational readiness scope into ... P6 and Smartsheet for project scheduling software + Experience working in a GMP environment + Experience with capital project execution. + Strong written and verbal… more
- Niagara Bottling LLC (Jeffersonville, IN)
- …as required by management. + Compliant to all safety rules and regulations, GMP 's and all Niagara policies and procedures. + Establishes and maintains high standards ... of Niagara's LIFE competency model, focusing on the following key drivers of success: + Lead Like an Owner + Makes safety the number one priority + Keeps alert for… more
- Graham Packaging Company (Elwood, IN)
- …we do-together-to create a better tomorrow. Working at Graham means you lead constructively with clear goals, use diverse thinking to drive excellence, ... + Understands, follows and enforces all established safety, health, quality GMP and Company policies, procedures and recognized practices. + Understands, follows… more
- Lilly (Indianapolis, IN)
- …the risks when making business choices and decisions. **Safety and Quality Culture:** + Lead by example in building and driving a culture of safety first and quality ... always within the organization. + Author, Review and/or approve GMP documentation including procedures, deviation investigations, technical reports, design reviews,… more