- Otsuka America Pharmaceutical Inc. (Springfield, IL)
- …degree and 15+ years of experience in a FDA regulated pharmaceutical and/or medical device industry environment + Strong knowledge of current global Good ... Summary** We are seeking an experienced and dynamic Executive Director of R&D Global Quality to join...Previous experience of working in the global pharmaceutical and medical device industry. + Experience working with… more
- Abbott (Abbott Park, IL)
- …to drive teams to action while working both within the constraints of medical device regulation, and within a highly matrixed environment with cross-functional ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… more
- Edwards Lifesciences (Chicago, IL)
- …for (Preferred):** + Deep engineering experience, with a strong background in medical device development. Experience in implantable sensors for cardiac ... engineering, and principles and practices + Knowledge and understanding of relevant medical device regulations (21 CFR Part 820), and standards (ISO 13485, IEC… more
- Bausch + Lomb (Springfield, IL)
- …with relevant global team members, other B&L departments (eg, R&D /Project Management, Clinical/ Medical Affairs, Biometrics, Regulatory Affairs, Quality ... areas to provide input on study-related documents and issues (DMP, SAP, drug/ device supplies, CSR, etc.). + Provides clinical operations input in the identification,… more
- AbbVie (North Chicago, IL)
- …medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's ... may include small molecule pharmaceuticals and/or biologics products, combination products, and medical devices to ensure business objectives are met with regards to… more
- Lundbeck (Deerfield, IL)
- …bachelor's degree. + 10+ years R&D experience within a pharmaceutical, medical device , and/or biotech industry. + 5+ years' experience in Regulatory ... Director Regulatory Affairs Alliance and Commercialization Requisition ID:...compliance directions for alliance portfolio and external communication materials, medical and scientific messaging, sales and marketing training, sample… more
- Philips (Chicago, IL)
- …You've acquired 10+ years of experience working in Regulatory Affairs within the medical device industry; Experience with software-enabled medical devices, ... ** Director , Regulatory Affairs- Software and Artificial Intelligence (Ultrasound)**...partnerships between Regulatory Affairs and all key stakeholders including R&D , Product Management, Quality, Medical & Clinical… more
- AbbVie (North Chicago, IL)
- …medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's ... Tok (https://www.tiktok.com/@abbvie) . Job Description The Pharma Product Group Associate Director will be fully accountable for providing CMC leadership and… more
- Edwards Lifesciences (Naperville, IL)
- …use, cath lab/OR environment and procedural best practices + Understanding of medical device asset creation, regulation requirements for claims and training ... ** Director , Global Professional Education and Sales Training -...and delivery. + Collaborate with internal teams (Marketing, Compliance, R&D and Sales). Build external relationships with HCPs and… more
- Fujifilm (Springfield, IL)
- …senior product manager, product/technical director ). + Minimum 8 years of medical device experience with strong clinical background. + Prior experience in ... R&D , operations, regulatory, global marketing, infection control, other companies/ device manufacturers, etc.) + Build and maintain strong relationships with Key… more