- Abbott (Sylmar, CA)
- …of device and Cardiac Rythm Management solutions The Opportunity - We are seeking a Regulatory Affairs Project Manager to join our Cardiac Rythm ... Management team in Sylmar CA. As an individual contributor, the function of a Regulatory Affairs Project Manager is to combine knowledge of scientific, … more
- AbbVie (Irvine, CA)
- …Instagram, YouTube, LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The Manager , Regulatory Affairs for Chemistry Manufacturing & ... implements, and documents policies and procedures within the regulatory affairs department under supervision of manager . Participates in initiatives internal… more
- Grifols Shared Services North America, Inc (Orange, CA)
- …8 or more years of experience in positions of increasing responsibility within Regulatory Affairs or related field within the Biologics, Biotech or ... Hiring Ordinance.** Learn more about Grifols (https://www.grifols.com/en/what-we-do) **Req ID:** 527460 **Type:** Regular Full-Time **Job Category:** Regulatory Affairs… more
- Edwards Lifesciences (Irvine, CA)
- …and how our products transform patients' lives. As part of our Clinical Affairs team, you'll hone your scientific curiosity and passion for evaluating data to ... with principal investigators, dedicated medical professionals, patient advocacy groups, and regulatory authorities, you will drive the evidence needed to optimize… more
- Terumo Neuro (Aliso Viejo, CA)
- …with Associates across all departments in R&D, Operations, Quality, and Regulatory Affairs to achieve company objectives and resolve project issues. + Manage ... **12788BR** **Title:** Manager , Engineering R&D **Job Description:** Manage individuals from...development through the application of the scientific process and project management. Job duties: + Manage a group of… more
- Edwards Lifesciences (Irvine, CA)
- …and how our products transform patients' lives. As part of our Clinical Affairs team, you'll hone your scientific curiosity and passion for evaluating data to ... with principal investigators, dedicated medical professionals, patient advocacy groups, and regulatory authorities, you will drive the evidence needed to optimize… more
- J&J Family of Companies (Irvine, CA)
- …+ Collaborate closely with functional areas, including Marketing, Therapy Advancement, Clinical Affairs , Medical Affairs , Regulatory , and R&D, to ensure ... & Johnson MedTech - Electrophysiology, is seeking a Marketing Manager , Event Strategy to join our team in Irvine,...Event Strategy will assist in driving the strategic formulation, project management, and execution of all US Commercial customer… more
- Medtronic (Northridge, CA)
- …engineering (mechanical, electrical, firmware, software, manufacturing), operations, marketing, clinical regulatory affairs , quality and other key business ... Venture programs. In this exciting role as a Program Manager , you will have responsibility for providing program leadership...medical device domain + Strong program management skills + Project Management Certification, such as PMP + MBA or… more
- Edwards Lifesciences (Irvine, CA)
- …and how our products transform patients' lives. As part of our Clinical Affairs team, you'll hone your scientific curiosity and passion for evaluating data to ... with principal investigators, dedicated medical professionals, patient advocacy groups, and regulatory authorities, you will drive the evidence needed to optimize… more
- Edwards Lifesciences (Irvine, CA)
- …and how our products transform patients' lives. As part of our Clinical Affairs team, you'll hone your scientific curiosity and passion for evaluating data to ... with principal investigators, dedicated medical professionals, patient advocacy groups, and regulatory authorities, you will drive the evidence needed to optimize… more
- Edwards Lifesciences (Irvine, CA)
- …and how our products transform patients' lives. As part of our Clinical Affairs team, you'll hone your scientific curiosity and passion for evaluating data to ... with principal investigators, dedicated medical professionals, patient advocacy groups, and regulatory authorities, you will drive the evidence needed to optimize… more
- AbbVie (Irvine, CA)
- …strong medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie's customers, markets, business operations and emerging issues. ... Oversee project -related training of investigators, study site personnel, and AbbVie...scientific content of protocols, Investigator Brochures, Clinical Study Reports, regulatory submissions and responses and other program documents. Lead… more
- AbbVie (Irvine, CA)
- …strong medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie's customers, markets, business operations, and emerging issues. ... Oversee project -related training of investigators, study site personnel, and AbbVie...scientific content of protocols, Investigator Brochures, Clinical Study Reports, regulatory submissions and responses, and other program documents. Experience… more
- Medtronic (Irvine, CA)
- …complex technical problems, collaborating closely with cross-functional teams including Manufacturing, Regulatory Affairs , R&D, and Supplier Quality to determine ... methodologies, statistics, and data analysis to ensure product safety and regulatory compliance. This role also involves close collaboration with cross-functional… more
- Edwards Lifesciences (Irvine, CA)
- …products and therapies + Interface with R&D, manufacturing, clinical development, clinical affairs , quality and regulatory personnel to ensure compliance with ... testing, fatigue test to success etc. + Work with project teams as a subject matter expert (SME) to...reduce conservatism + Be an SME in communication with regulatory bodies + Mentor other engineers and technicians +… more
- Edwards Lifesciences (Irvine, CA)
- …and how our products transform patients' lives. As part of our Clinical Affairs team, you'll hone your scientific curiosity and passion for evaluating data to ... with principal investigators, dedicated medical professionals, patient advocacy groups, and regulatory authorities, you will drive the evidence needed to optimize… more