- Lilly (Indianapolis, IN)
- …are determined to make life better for people around the world. The Associate Director - Quality - Indianapolis Device Manufacturing Device Quality ... Lab is primarily responsible for quality control oversight of the Device Quality Laboratory. **Responsibilities:** + Provide leadership of IDM Device … more
- Lilly (Indianapolis, IN)
- …the world. **Position Brand Description:** The IDM (Indianapolis Device Manufacturing) Quality Assurance Associate Director is primarily responsible for ... quality assurance and quality control oversight of device contract manufacturing (CM) organizations including molding, sub-assembly and assembly operations.… 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 ... leadership will be instrumental in mentoring a technical staff and overseeing device assembly processes to ensure control and capability. **Key Objectives and… more
- Lilly (Indianapolis, IN)
- …Project Management skills + Familiarity and practical experience with medical device / combination product quality & regulatory requirements, including ... leadership for Commercialization Global Program Managers (GPM's) who lead medical device and drug/ device combination product commercialization actives through… more
- Lilly (Indianapolis, IN)
- …be part the Global Quality QC Operations team reporting directly to the Associate Vice President of Global Quality QC Operations and you'll have a dotted ... line relationship to the Senior Vice Presidents of Global Quality for the Parenteral and Device Networks. You'll be an integral member of the AQCO team and with… more
- Merck (Indianapolis, IN)
- …regulatory updates. + Audit vendors/partners of SaMD/IVD/Companion Diagnostics **Reports to** - Director Regulatory Compliance, Device Quality and Regulatory ... **Job Description** This position will be part of the Device Quality & Regulatory Team within Global Regulatory Affairs and Clinical Safety (GRACS). The primary… 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 ... journey. In this role within our Device and Packaging Network, you'll not only execute strategies...influence and implement our organizational agenda, business priorities, and quality objectives to drive success down to the floor… more
- United Therapeutics (Indianapolis, IN)
- …), livers ( **miroliver(R)** ), and a bioengineered external liver assist device for acute liver failure ( **miroliver** **_ELAP_** **(R)** ), with plans ... regulatory experience with a Bachelor's Degree in life sciences, quality , regulatory affairs or a related area of study...regulatory experience with a Master's Degree in life sciences, quality , regulatory affairs or a related area of study… more
- Otsuka America Pharmaceutical Inc. (Indianapolis, IN)
- …and/o academic translational clinical research experience (as a general guideline, 1-3 years for Associate Director level; 3-6 years for Director and 6-9 ... While not essential, prior personnel management experience, will support position at entry ( Associate Director / Director ). + An advanced understanding of drug… more
- Lilly (Indianapolis, IN)
- …for the External Manufacturer. + Inform TS/MS (Technical Service/Manufacturing Science) Associate Director about project status and issues. **Department ... + Define and own the process control strategy, including key parameters and quality attributes. + Understand product history and potential failure modes. + Educate… more