- Cardinal Health (Topeka, KS)
- **_What Regulatory Affairs and Clinical Submissions contributes to Cardinal Health_** The _Manager, Regulatory Affairs ( Clinical Submissions)_ is ... or timelines. + **Leadership & Team Development** + Lead, mentor, and develop junior regulatory affairs staff, providing training and guidance on regulatory … more
- Veterans Affairs, Veterans Health Administration (Leavenworth, KS)
- …as a Supervisory Health Systems Specialist - Credentialing and Privileging Manager . They oversee all functions related to healthcare providers' professional ... are efficiently and effectively accomplishing quality work that is compliant with regulatory requirements and procedures, TJC standards, laws, and VHA C&P policies… more
- Sumitomo Pharma (Topeka, KS)
- …of expiry dates and communicates changes to contract manufacturing organizations, testing laboratories, clinical sites and regulatory affairs as needed. + ... and suppliers of drug substances and drug products used for investigational clinical trials and/or commercial phases. The Senior Manager ensures compliance… more
- Edwards Lifesciences (Topeka, KS)
- …our innovations and how our products transform patients' lives. As part of our Clinical Affairs team, you'll hone your scientific curiosity and passion for ... clinical trials with skill levels exceeding the requirements of the Associate Manager Required + Experience in clinical trial design, indication lead +… more
- Eurofins (Lenexa, KS)
- …robust and clinically meaningful results available + Develop effective working relationship with Regulatory Affairs to assure that clinical lab is ... forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global...Basic Function and Scope of Responsibility: The Laboratory Operations Manager is primarily responsible for successful day to day… more
- Fujifilm (Topeka, KS)
- …+ Proven track record working with Marketing, Business Development, Engineering/QA, and Regulatory Affairs . + Competitive knowledge of Medical IT and Imaging ... US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements and all...at least 1-2 years direct experience as a Product Manager within HCUS/MIPD + Strong understanding of clinical… more