- 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 ... application should be directed to Chat with Ripley. R1595528 : Associate Director of Validation **Company:** Bristol-Myers Squibb **Req Number:** R1595528… more
- Lilly (Indianapolis, IN)
- …solutions to support communities through philanthropy and volunteerism. **Outline of Role:** Associate Director , Joint Process Team (JPT) is responsible for ... - External API Manufacturing Operations (who is also located at the Kinsale site). The Associate Director , JPT is the key business relationship owner with the of… more
- Lilly (Indianapolis, IN)
- …Lilly and Active Pharmaceutical Ingredient (API) Contract Manufacturer representatives. The JPT Associate Director is the key business relationship owner and is ... materials are delivered on time and within downstream customer expectations. The JPT Associate Director will partner with Lilly's Process Research & Development… more
- Bristol Myers Squibb (Indianapolis, IN)
- …your application should be directed to Chat with Ripley. R1596697 : Associate Director , IT Regulatory, Clinical, and Enterprise Systems **Company:** ... aims to be the global leader in radiopharmaceuticals. **Job Description** The Assoc. Director , IT Regulatory, Clinical and Enterprise Systems is an integral part of… 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)
- …world. Eli Lilly and Company is seeking an experienced and highly motivated Associate Director to join our Technical Services/Manufacturing Science (TS/MS) team, ... peptide processes from development to manufacturing, ensuring successful scale-up, validation , and regulatory compliance. * Design, execute, and interpret… more
- Lilly (Lebanon, IN)
- …a successful startup into GMP manufacturing operations._ **Position Description:** The Associate Director - Technical Services/Manufacturing Science (TSMS) is ... responsible for managing the activities of TSMS personnel. The Associate Director TSMS must balance coaching a technical staff, prioritization and staffing for… more
- Lilly (Indianapolis, IN)
- …mentoring to drive analytical initiatives and improvements. The Quality Control (QC) Associate Director (AD) Analytical Sciences is responsible for leading the ... and quality systems. **Additional Preferences:** + Experience in method development and validation + Experience with a broad range of analytical techniques +… 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
- Lilly (Indianapolis, IN)
- …who are determined to make life better for people around the world. As the Associate Director - Test Methods/Systems in IDM you will oversee and coordinate the ... teams). + Mechanical aptitude (knowledge of mechanical equipment, controls, and validation for medical devices). + Knowledge of manufacturing processes (preferably… more
- Lilly (Indianapolis, IN)
- …with CMs to ensure alignment of intents and objectives. + Validation : ensure proper definition of strategies, revisions, protocol approvals, validation ... External Manufacturing documentation (eg, Quality Agreements, Manufacturing Requirements Document, validation documents) is in place and in compliance. + Build… more
- Otsuka America Pharmaceutical Inc. (Indianapolis, IN)
- …Profound grasp of Machine Learning lifecycle - feature engineering, training, validation , scaling, deployment, scoring, monitoring, and feedback loop. + Have ... implemented machine learning projects from initiation through completion with particular focus on automated deployment and ensuring optimized performance. + Agile skills and experience + Experience in Healthcare (esp. US) industry is a plus. **Competencies**… more
- GRAIL (Indianapolis, IN)
- …and other stakeholders to support regulatory strategy development, product validation , audits, promotional material review, on-market product support, and change ... control processes. This individual monitors and communicates changes in regulatory policies and In Vitro Diagnostic (IVD) requirements to project teams and leadership. They may manage and provide direction to regulatory staff and, when required, participate in… more
- Humana (Indianapolis, IN)
- …Lead Medical Director , depending on the line of business. The Medical Director conducts Utilization Management or clinical validation of the care received by ... of our caring community and help us put health first** The Medical Director actively uses their medical background, experience, and judgement to make determinations… more
- Bristol Myers Squibb (Indianapolis, IN)
- …lives. Read more: careers.bms.com/working-with-us . RayzeBio is seeking a Sr Associate Scientist 1- Microbiology, reporting to the Director - Microbiology ... role will also involve advanced laboratory analyses, troubleshooting efforts, method validation and qualifications ensuring compliance with regulatory and QA system… more
- Lilly (Indianapolis, IN)
- …and documenting and maintaining the state of process/sterility assurance/cleaning validation . **Key Objectives / Deliverables:** + Responsible for maintaining a ... initiatives for staff + Communicate effectively with Parenteral TS/MS Network Director and other Parenteral TS/MS leaders to ensure alignment of technical… more
- Sumitomo Pharma (Indianapolis, IN)
- …Master Files (TMFs) ready for audits and inspections. Partnering with the Associate Director , Clinical Business Operations, the specialist ensures accountable ... UAT as needed and collaborate with Information Technology to ensure system validation is maintained. + Work closely with Clinical Operations and Regulatory Affairs… more