- Lilly (Pleasant Prairie, WI)
- …driving solutions that impact the site and align with corporate objectives. The Associate Director , Quality Assurance, will also provide computer system quality ... impact the site and align with corporate objectives. The Associate Director , Quality Assurance, will also provide...Minimum 5 years working in the pharmaceutical or medical device industry in QA roles + Minimum 3 years… more
- Lilly (Indianapolis, IN)
- …to make life better for people around the world. **Lead the Indianapolis Device Manufacturing organization's activities and personnel for device , cartridge, and ... containers. + Establish and maintain standards for developing, validating, and transferring device analytical methods and test systems. + Ensure qualified state of… more
- Bristol Myers Squibb (Devens, MA)
- …lives. Read more: careers.bms.com/working-with-us . **Position Summary** Reporting to the Director , Inspection Readiness, the Associate Director will ... and collaborate extensively with teams and leaders across the BMS network. The Associate Director will support BMS' GMP/GDP Inspection Readiness strategy by… more
- GRAIL (Concord, NH)
- …position supports the US Regulatory team in preparing Investigational Device Exemptions (IDEs), IDE supplements, pre-submissions, Premarket Approvals (PMAs), annual ... 510(k)s, post-approval reports, annual reports, export certificates, establishment registrations, and device listings. + Serve as a key member of the Regulatory… more
- Otsuka America Pharmaceutical Inc. (Baton Rouge, LA)
- The Associate Director of Regulatory Intelligence leads the collection and dissemination of regulatory intelligence and collaborates with SMEs to interpret the ... EFPIA, JPMA, etc.). + Demonstrate solid working knowledge of the drug , biologic, and device development process, laws, regulations, and guidelines from FDA, EMA,… more
- AbbVie (North Chicago, IL)
- …YouTube, LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The ME&C Associate Director is a global program management expert responsible ... and execution of Biologics and/or Toxin industrialization programs with experience in drug substance and/or drug product transfers. The program manager is… more
- BD (Becton, Dickinson and Company) (San Diego, CA)
- …needed, reducing inefficiency and waste for nursing and pharmacy teams. As the ** Associate ** ** Director , R&D -** you will manage activities across a complex ... to reduce the spread of infection, improve diabetes treatment and advance drug delivery. With our technical capabilities, the Medication Management Solutions (MMS)… more
- Lilly (Concord, NC)
- …team operates, now is the perfect opportunity! During the project phase, the Associate Director (AD), Operations is responsible for staffing, training, and ... which will house warehousing & logistics, operations including parenteral, medical device assembly, and packaging, QC laboratories, and support teams to produce… more
- GE HealthCare (Bellevue, WA)
- …development and familiarity with Software Development Lifecycle (SDLC) in medical device or healthcare software development environment. + Experience with Agile/Lean ... is preferred. + Demonstrated understanding or aptitude to understand Medical Device QMS requirements and regulatory requirements including but not limited to… more
- Takeda Pharmaceuticals (Cambridge, MA)
- … Drug Safety, Clinical Sciences, Outcomes, Digital Health, Pharmaceutical Sciences/ Device , and Global Regulatory Affairs. * Advanced knowledge of regulatory ... Position Objectives: * Leads strategic, scientific, and operational aspects of multiple drug development projects with a high level of technical and strategic… more