- Bristol Myers Squibb (Indianapolis, IN)
- …entrepreneurial team, RayzeBio aims to be the global leader in radiopharmaceuticals . The Associate Director of Validation is responsible for leading the ... and company standards for pharmaceutical/radiopharmaceutical production. This role oversees validation activities from initial planning through execution, manages a… more
- Lilly (Lebanon, IN)
- …while also reducing costs and environmental impact. The Associate Director -Automation Engineering - Control System Validation and Data Analytics, is ... that support the daily operations of the facility. The Associate Director is also responsible for the...including recruiting, resource planning, and succession planning. * Process validation and CSV work coordination. * Review and monitor… more
- Otsuka America Pharmaceutical Inc. (Indianapolis, IN)
- **Job Summary** **** The Associate Director , MSAT - Downstream provides specialized technical leadership and oversight for all downstream manufacturing ... and compliance of downstream operations through effective technology transfer, validation support, process monitoring, troubleshooting, and lifecycle management activities… more
- Lilly (Indianapolis, IN)
- …solutions to support communities through philanthropy and volunteerism. **Outline of Role:** Associate Director , Joint Process Team (JPT) is responsible for ... and reports into the Sr. Director - External API Manufacturing Operations. The Associate Director , JPT is the key business relationship owner with the of… more
- Lilly (Lebanon, IN)
- …trial medicines, while also reducing costs and environmental impact. The Associate Director -Automation Engineering - Control System Hardware, I&C, Projects ... of the facility and managing the overall Automation Portfolio and Projects. The Associate Director is also responsible for the productivity and development of… more
- Lilly (Indianapolis, IN)
- …determined to make life better for people around the world. The purpose of the Associate Director - Safety Data Scientist is to manage and analyze complex Global ... issues, and drive analytic solutions. The Safety Data Scientist Associate Director / Director will...needed. + Partners with Quality to ensure that standard validation principles and system development methodologies are utilized to… more
- Lilly (Indianapolis, IN)
- …as we achieve drug product manufacturing and commercialization excellence. As the Associate Director of Technical Services/Manufacturing Science (TS/MS) in the ... procedures, deviation investigations, technical reports, change controls, regulatory submissions, validation protocols and summary reports, PFDs, APRs, etc. +… more
- Lilly (Indianapolis, IN)
- …lead the charge in shaping the future of manufacturing at Eli Lilly? As an Associate Director of Engineering, you'll be at the forefront of this exciting ... procedures, deviation investigations, technical reports, change controls, regulatory submissions, validation protocols and summary reports, PFDs, APRs, etc. 4.… more
- Lilly (Indianapolis, IN)
- …to support communities through philanthropy and volunteerism. **Responsibilities** **The Associate Director - Technical Services/Manufacturing Science (TS/MS) ... supporting the oversight of external manufacture of dry products. The Assoc. Director TSMS must balance coaching a technical staff, prioritization and staffing for… more
- Lilly (Indianapolis, IN)
- …solutions to support communities through philanthropy and volunteerism. **Responsibilities:** The Associate Director - API EM Engineering Leader for Peptides ... processes, and functions. + Direct or indirect experience with commercialization ( Validation , Tech Transfer, CMC, GMP, Quality, and/or HSE) + Demonstrated ability… more
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