- GE HealthCare (Waukesha, WI)
- …experience is preferred. Demonstrated understanding or aptitude to understand Medical Device QMS requirements and regulatory requirements including but not limited ... / production process control methodologies, and servicing in a medical device environment. Experience in a global working environment. + Experience leading… more
- AbbVie (North Chicago, IL)
- …Pharmaceutical Ingredients (API), produced by AbbVie or third-party manufacturer Intermediates/ Drug Products. Acts as the principle, quality, global supply chain ... compliance and regulatory conformance issues for sterile, biological, liquid, solids, and/or device products and elevates medium and high risk events to AbbVie… more
- Lilly (Indianapolis, IN)
- …lead aspects scope development, design, delivery, and optimization of manual and automated device assembly processes and related equipment in support of IDM and ... Device network objectives for product commercialization, capacity expansion, and...vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (eg, healthcare and/or dependent day… more
- Amgen (Washington, DC)
- …regulations + Drive the development of and end-end process/playbook to conduct combined drug and device trials + Conduct gap assessments of current ... Join us and transform the lives of patients while transforming your career. ** Director IVD Strategy & Operations - Precision Medicine Unit** **What you will do**… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …areas centered around rare diseases and immune disorders. **Job Summary:** The Director of Data Management (DM) Reporting provides leadership in Data Management ... external data acquisition and validation, and tools to support project portfolio across drug programs. This role is responsible for ensuring the quality and timely… more
- Lilly (Indianapolis, IN)
- …conduct of clinical trials. + Broad understanding of the pharmaceutical drug / device development process + Prior experience in managing complex/cross-functional ... partnerships and influence with asset team leadership (eg team leader, COO, medical director , lead CRP) and cross-functional team members from across the CDDA. The… more
- Takeda Pharmaceuticals (Boston, MA)
- …with portfolio teams to optimize top-tier development cycle times to accelerate drug to patients. **Accountabilities:** + Senior level R&D CMC portfolio strategy ... as ADCs and combination products consisting of simple to complex device elements). + Autonomously collaborates, mentors and champions CMC-leads/teams to influence… more
- Bausch Health (Bridgewater, NJ)
- …it-where your skills and values drive our collective progress and impact. The Director , Medical Affairs, will play a pivotal role in developing and implementing ... industrial experiences + Proven experience in medical affairs within medical device industry. + Strong understanding of clinical development and commercialization… more
- Stryker (Portage, MI)
- **Who we want:** The ideal candidate for the Director of New Product Development Operations is a dynamic and strategic leader with a proven track record in managing ... and execution for multiple product segments / business function. **Med Device Compliance:** * Influence internal regulatory requirements and industry standards such… more
- Abbott (Cleveland, OH)
- …products for treatment of vascular disease. Our extensive portfolio includes drug -eluting stents, guide wires, balloon dilatation catheters, imaging catheters and ... devices. We currently have an opportunity available for a **Coronary Regional Sales Director in Ohio.** This role will report to the Area Vice President. The… more