Role Summary
Operations Associate - IDM at Lilly. Responsible for working with Contract Manufacturer(s) to support supply, quality, and continuous process improvement of delivery devices, sub-assemblies, and components supplied to Lilly packaging and manufacturing sites.
Responsibilities
- Facilitate the Joint Process Team between Lilly and the Contract Manufacturer
- Supervise and communicate monthly JPT metrics
- Foster and support strong Safety and Quality Cultures at the CMs
- Provide day to day oversight of activities and resolve issues occurring between the CMs and Lilly sites
- Lead the resolution of manufacturing related issues, including deviations, evaluation of manufacturing data and supply chain daily/weekly issues
- Trained to perform TrackWise activities such as Lead investigator and Change Owner
- Provide operations project management input and oversight for capital projects at CMs
- Work with engineering, product stewards and others in the development/leading of process/product improvements. This may include project planning activities, development of protocols, coordination of internal and external lab based testing, documentation of the data and completion of technical reports
- Track completion of documentation and process updates resulting from local and global procedural changes, audits, complaint investigations, documentation reviews, product reviews, process reviews and equipment reviews
- Develop effective and productive working relationships with colleagues at CM sites
- Lead multi-functional/cross-site/cross-company project teams as needed
- Provide backup, as appropriate, for the Manager βΓΓ¬ CMO Operations
Qualifications
- BachelorβΓΓ΄s Degree required in a STEM / technical field
- 2 or more years manufacturing experience preferred
- Demonstrated high degree of ownership / accountability
- Strong communication (written and oral) skills, teamwork, and influence
- Solid technical writing skills
- Ability to organize and prioritize multiple tasks
Additional Preferences
- Previous Leadership/supervisory experience
- Career interest in operations or functional leadership
- Previous engineering or project management experience in medical devices
Other Information
- Travel required for visits to the CM (5 - 50%).