- Genentech (Boston, MA)
- …therapies that provide meaningful improvement to patients. The Lead Medical Director makes major contributions to development of the Clinical Development (CD) ... have a demonstrated understanding of Phase II - III drug development. + You will take an active role...will take an active role with other CST members, regulatory and other internal partners/stakeholders in the completion and… more
- Lilly (Indianapolis, IN)
- …make life better for people around the world. **Position Brand Description:** The Senior Director - QC Labs IPM is responsible for the oversight and execution of the ... in-process samples, semi-finished and finished products, physical and functional testing of Drug / Device combination product and visual and physical testing of… more
- Lilly (Lebanon, IN)
- …the Lilly Medicine Foundry, a new center for advanced manufacturing and drug development. The first-ever facility of its kind, combining research and manufacturing ... from design, to start-up, and to steady-state operations. The Senior Director , Analytical GMP Laboratories position seeks a collaborative, inclusive, energetic… more
- Lilly (Indianapolis, IN)
- …candidates to lead unit operation development and process optimization of synthetic drug candidates to support clinical trials, regulatory submission, and ... synthetic active pharmaceutical ingredients from pre-clinical phases through commercialization of drug substances and drug products. Our scientists and engineers… more
- Otsuka America Pharmaceutical Inc. (Albany, NY)
- **Job Summary** We are seeking an experienced and dynamic Executive Director of R&D Global Quality to join our team. This pivotal role will be responsible for ... trial and submission support, lead the R&D audit program, engage with regulatory authorities, and maintain clinical data integrity. The leader will be responsible… more
- Sanofi Group (Morristown, NJ)
- **Job Title:** Principal Medical Writer Associate Director **Location** : USA, Remote. Proximity to Cambridge/Boston, MA or Morristown, NJ is highly desirable for ... of medicine? The race is on to speed up drug discovery and development to find answers for patients...serves to generate timely, high quality, cost effective and regulatory compliant documents. Our mission is to synergize and… more
- Lilly (Indianapolis, IN)
- …better for people around the world. **Overview of Role:** The Senior Director , QMS Operational Controls will provide central oversight of Operational Controls ... Trainings, and implementation tools are implemented and maintained according to regulatory , industry, and company expectations. + Implement and continuously improve… more
- Fresenius Medical Center (Baton Rouge, LA)
- …programs in an assigned area ensuring compliance with established company and regulatory guidelines and procedures in order to provide high quality dialysis services ... of area while ensuring compliance with all pertinent company policies and regulatory requirements. In partnership with the Business Leadership team responsible for… more
- Lilly (Indianapolis, IN)
- …Global Data Analytics & AI Organization (DIA) is actively seeking an **Associate** ** Director of Data, Analytics & AI (Quality)** to lead the digital transformation ... prediction, deviation analysis, complaint insights) aligned with corporate quality and regulatory goals. + **Define and Deliver High-Value Data Products:** You will… more
- Gilead Sciences, Inc. (Foster City, CA)
- …Join Gilead and help create possible, together. **Job Description** The Director , Clinical Development - Inflammation will lead the design, execution, and ... key role in shaping clinical strategy, collaborating cross-functionally with research, regulatory , safety, and commercial teams to advance innovative therapies that… more