- Otsuka America Pharmaceutical Inc. (Indianapolis, IN)
- …content and context required of promotional labeling materials for prescription drug and medical device products. Must be effective in managing work and ... context required of promotional labeling materials for prescription drug and medical device products. Must be effective in managing work and resolving conflicts.… more
- Lilly (Indianapolis, IN)
- …a manufacturing environment + Awareness of GMP and ISO requirements related to medical devices and device assembly operations Additional Preferences: + Previous ... lead aspects scope development, design, delivery, and optimization of manual and automated device assembly processes and related equipment in support of IDM and … more
- Otsuka America Pharmaceutical Inc. (Indianapolis, IN)
- …the clinical safety, efficacy, medical usefulness and value of drug or medical device product candidates. + Interpret and communicate results of Phase I-IV ... with a focus on pharmaceutical products to meet unmet medical needs and nutraceutical products for the maintenance of...research experience (as a general guideline, 1-3 years for Associate Director level; 3-6 years for … more
- Otsuka America Pharmaceutical Inc. (Indianapolis, IN)
- …the clinical safety, efficacy, medical usefulness and value of drug or medical device product candidates. + Interprets and communicates results of Phase I-IV ... protocols. + Develops focused expertise to serve as an clinical/ medical scientific consultant to health economic, medical ...research experience (as a general guideline, 1-3 years for Associate Director level; 3-6 years for … more
- Lilly (Indianapolis, IN)
- …strong partnerships and influence with asset team leadership (eg team leader, COO, medical director , lead CRP) and cross-functional team members from across the ... and publications. The Clinical Development Program Lead reports to the Associate Vice President within their assigned therapeutic area. **Key Responsibilities:** 1.… more
- Canon USA & Affiliates (Indianapolis, IN)
- …MS Word, Excel, Oracle, Sales Force, etc. + 2 Years Regulatory Affairs experience in medical device industry required + Minimum Education Level: 2 Year / ... - Post Market - req1434** **OVERVIEW** Reporting to the Director Regulatory Affairs, the Regulatory Affairs Specialist is responsible...Associate 's Degree + 4 Year/ Bachelor's Degree (STEM) preferred… more
- Lilly (Indianapolis, IN)
- …for the External Manufacturer. + Inform TS/MS (Technical Service/Manufacturing Science) Associate Director about project status and issues. **Department ... TS/MS management, product and technical leaders, GPLOT leaders, and molecule/ device stewards. **Basic Qualifications:** + Bachelor's Degree in Pharmacy, Chemistry,… more