Regulatory Affairs Assistant Salary at Act Labs BETA

Overview: Founded in 1965, UC Irvine is a member of the prestigious Association of American Universities and is ranked among the nations top 10 public universities by U.S. News & World Report. The campus has produced five Nobel laureates and is known for its academic achievement, premier research, innovation and anteater mascot. Led by Chancellor Howard Gillman, UC Irvine has more than 36,000 students and offers 224 degree programs. Its located in one of the worlds safest and most economically vibrant communities and is Orange Countys second-largest employer, contributing $7 billion annually to the local economy and $8 billion statewide. To learn more about UC Irvine, visit www.uci.edu. The UCI Center for Clinical Research was built on the belief that running clinical trials should be a seamless experience. We work across the UCI enterprise to offer patients, investigators, and industry partners the quick and effortless support they need to participate in and run successful clinical tr

Job Description Job Description REGULATORY SPECIALIST NEEDED FOR A VERY BUSY COSMETIC MANUFACTURER! CALL/TEXT MARIA AT 661-775-2570 ASAP! Duties: Assist in maintaining the Quality Management System and Regulatory Affairs Program. Maintain FDA, NRC, and CA-RHB product registrations and licensing. Author, review, and submit License applications and Regulatory product registrations. Liaise and communicate with regulatory agencies and customers regarding licensing inquiries, product registrations, and import and export compliance regulations. Maintain/support EZIP’s Quality System documentation. Maintain technical files for CE Marking/medical devices and other products. Create and edit procedures/forms. Support Customer Contact Program. Evaluate customer complaints and communicate the results of corrective action evaluations, conformance to product specifications, and preventive actions taken. Maintain CAPA system including issuance, follow-up, and closure of CAPAs. Lead auditor for intern

Overview: In collaboration with the Directors, Unit Supervisors and/or Director of Nursing, this position is responsible for staffing nursing areas. Effectively performs all tasks required to provide staffing that meets regulatory agency and hospital standards. Is also responsible for assuring that the bodies of deceased patients are legally and expediently released to the appropriate agency. This position requires the full understanding and active participation in fulfilling the Mission of SGVMC. It is expected that the employee demonstrate behavior consistent with the Core Values. The employee shall support SGVMCs strategic plan and the goals and direction of the performance Improvement Plan (PIP). Responsibilities: Specific Job Duties: Initiates daily nursing office activity sheet and updates throughout the day. (Sends to nursing office report group the following day) Maintain licenses, certifications, competencies of per diems, agency staff and travelers on file. Entry of all paper

Job Description Job Description Work Location: Sunnyvale, California Salary Range: $80,000 - $140,000 Job Type: Full-Time Onsite Our Company: Founded in 2010, iHealth Labs is dedicated to empowering people to live healthier lives. The company is a leading provider of cloud-connected medical devices, personal health care devices, and home-based tests and is at the forefront of the digital health revolution. In November 2021, iHealth's COVID-19 Antigen Rapid Test received Emergency Use Authorization from the U.S. Food and Drug Administration for over-the-counter sales. Since then, iHealth has become a key supplier of at-home COVID tests to the federal government, state governments, nonprofits, and individual consumers. iHealth Labs is a leader in digital health solutions, with a mission to revolutionize the healthcare industry by making quality health management accessible and affordable for all. Job Responsibilities: In this role, you will be part of the regulatory team responsible for

Job Description Job Description REGULATORY SPECIALIST NEEDED FOR A VERY BUSY COSMETIC MANUFACTURER! CALL/TEXT MARIA AT 661-775-2570 ASAP! Duties: Assist in maintaining the Quality Management System and Regulatory Affairs Program. Maintain FDA, NRC, and CA-RHB product registrations and licensing. Author, review, and submit License applications and Regulatory product registrations. Liaise and communicate with regulatory agencies and customers regarding licensing inquiries, product registrations, and import and export compliance regulations. Maintain/support EZIP’s Quality System documentation. Maintain technical files for CE Marking/medical devices and other products. Create and edit procedures/forms. Support Customer Contact Program. Evaluate customer complaints and communicate the results of corrective action evaluations, conformance to product specifications, and preventive actions taken. Maintain CAPA system including issuance, follow-up, and closure of CAPAs. Lead auditor for intern

Job Summary: The Director Ambulatory Practice supports the Medical Group Administrative Team as the recognized leader in understanding and interpreting standards for ambulatory clinical practice, as well as applying, evaluating and improving those standards to ensure ambulatory clinical practices meet all regulatory requirements and organizational policies and procedures, concurrently supporting the quality, service and financial goals and objectives of Kaiser Permanente. For the Medical Office Buildings and other ambulatory hospital-based settings associated with the Medical Center, the Director Ambulatory Practice is accountable for designing , implementing, evaluating and improving systems, methods and strategies to maintain and improve the compliance of ambulatory care service delivery, clinical quality, clinical processes/systems, performance, patient satisfaction / safety, practice standards and the effectiveness of patient care with regulatory and organizational / institutional

**Overview** MedAlliance, in partnership with Cordis, specializes in the development of ground-breaking technology and commercialization of advanced drug device combination products for the treatment of coronary and peripheral artery disease. Our mission is to revolutionize healthcare by creating next-generation solutions that address unmet and critical medical needs. MedAlliance is headquartered in Switzerland, with offices in Germany, Singapore, UK and the United States (Irvine, CA). If you love a challenge and are ready to have a direct, positive impact on the lives of millions, then this is the place for you. Join us, and let's improve the wellbeing of millions, together. We are the people behind the people who keep saving lives. ****Prefer someone in Irvine, CA but open to remote.**** MedAlliance (Cordis) are seeking a highly skilled and motivated Principal Regulatory Affairs Specialist to join our dynamic team. This role will play a crucial part in preparing and submitting PMA mo

USC's Zilkha Neurogenetic Institute (ZNI) is seeking a Research Associate to join its team at the Health Sciences Campus. ZNI is the recipient of two large, multi-center, multi-year program project grants. This grant-funded position, under the guidance of Drs. Zlokovic and Toga, will develop business models to efficiently manage the program's business activities including day-to-day activities, contractual agreements, allocation of funds, and regular income/expense reports. The candidate will be required to assist with the preparation and submission of all grant-related reporting for these projects and will work with the PIs, department, sponsor and institution to provide assistance involving regulatory affairs and IRB processes, including protocol submissions, subject recruitment and coordination of MRI/PET studies across 4 different sites (Washington University, Banner Alzheimer's Institute, Mayo Clinic, USC). This position is the point of contact for all non-scientific business and