- Regeneron Pharmaceuticals (Tarrytown, NY)
- **Senior Director , Clinical Informatics and Health Data Sciences** The Regeneron Genetics Center uses genetics and health data on millions of people to advance our ... that will transform electronic health records, surveys, laboratory assays, or digital device data into a harmonized format compatible with RGC analytical tools,… more
- Fisher Associates (Buffalo, NY)
- …but not limited to, the decision to use or access a particular drug , device , or medical service), marital status, partnership status, caregiver status, ... Director of Land Development (Civil/Site) Buffalo, NY (http://maps.google.com/maps?q=55+Chicago+Street+Buffalo+NY+USA+14204) * Land Development Job Type Full-time… more
- Lilly (Indianapolis, IN)
- …to make life better for people around the world. The Indianapolis Device Assembly and Packaging Supply Chain function provides Materials Management services to ... production activities at the LTC-South Campus. The Associate Director - IDAP Supply Chain Customer Service provides leadership to the Site on Affiliate Order… more
- Wabtec Corporation (Germantown, MD)
- …you make a difference?** We are currently seeking an experienced and entrepreneurial Director of Product Management to help pioneer our entry into the emerging ... 7+ years of experience leading, managing, and growing IoT device solutions or similar technologies. + Minimum of 7+...employment is conditioned upon the successful completion of a drug screen (as applicable) and fitness for duty test… more
- AbbVie (North Chicago, IL)
- …Chemistry, Manufacturing and Controls (CMC) teams and Product Presentation and Device Strategy Teams (PPDST) of functional representatives from various departments ... may include new chemical entities (NCEs), new biological entities (NBEs), antibody- drug -conjugates (ADCs), toxins, and gene and cell therapies, incl. combination… more
- AbbVie (North Chicago, IL)
- …regulatory starting materials, Active Pharmaceutical Ingredients (API), Intermediates, and Drug Products produced by AbbVie plants or by third-party manufacturers, ... Quality Assurance strategy and implements agreed strategy to support pharmaceuticals, biologics, device and combination products produced at AbbVie plants as well as… more
- Abbott (Plymouth, MN)
- …product Design History File. + Comply with US Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, ... of leadership experience in Engineering, R&D, and/or Quality within a medical device /biomedical, high technology, and/or regulated industry + 5+ years in Program… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …has sufficient understanding of regulations and GCP requirements for drug development, advanced knowledge of Electronic Data Capture/related applications and ... ensure effective cross-functional collaboration and proactive communication throughout the drug development process. + Collaborates within the function and… more
- Bristol Myers Squibb (Madison, NJ)
- …years in the industry with at least 4+ years of US Medical Device Regulatory Affairs experience **Key Competencies** + Experience in successfully leading teams; ... objectives. + Experience with clinical trial assays (CTA) in drug clinical trials in communicating between Diagnostic sponsor and... clinical trials in communicating between Diagnostic sponsor and Drug sponsor. + Experience as a member of Global… more
- Takeda Pharmaceuticals (Lexington, MA)
- …profound GRA CMC knowledge underpinned by a deep understanding of global drug development and regulatory essentials to address and overcome challenges that arise ... Advanced Degree (MS), with Ph.D. preferred. + 15+ years of seasoned biopharmaceutical/ device industry experience or with a regulatory agency, while leading major… more