Displaying 1-10 of 1000 results
Inpatient Regulatory Affairs RN Manager
Clinical Management Consultants - San Francisco, California
A Northern California not-for-profit hospital is seeking a Regulatory Affairs Nurse Manager to join their team. The facility is part of an extended network of hospitals that provide quality care for patients in Northern and Central California. The Nurse Manager will be provide coordination for all aspects of regulatory involvement, including accreditation and licensure (Title 22). The RN Manager will interact and communicate with all licensing and regulatory entities, including but not limited to CMS, TJC, CDPH and OSHA. The Regulatory Affairs and Accreditation Manager will train survey … (see more)
Senior Project Manager, Regulatory Science - Acerta
AstraZeneca Pharmaceuticals LP - San Francisco, California
Legal / Law Related
Acerta Pharma is a leader in the field of covalent binding technology and is applying this technology to create novel, highly selective therapies for cancer. In February 2016, AstraZeneca acquired a majority share of Acerta Pharma via a USD $4 billion investment and is a committed partner to the development of these innovative drug candidates. Acalabrutinib is Acerta's lead program which was developed based on our discovery efforts. It is an investigational covalent Bruton tyrosine kinase (BTK) inhibitor currently under investigation in multiple Phase 3 clinical trials. The clinical program … (see more)
Manager, Regulatory Affairs
Dart NeuroScience LLC - San Diego, California
Legal / Law Related
Working in a team environment, the Regulatory Affairs Manager will be responsible for executing regulatory strategy as well as hands-on management of all technical and operational aspects related to the regulatory lifecycle (e.g., from preclinical candidate designation through registration) of assigned DNS products. Strategic Planning Represent the Regulatory Affairs department on multidisciplinary product development teams Participate in the development and implementation of regulatory strategy for one or more programs Research regulatory precedent related to product class and … (see more)
Manager, Global CMC Regulatory Affairs (1 of 3) - San Diego
J&J Family of Companies - San Diego, California
Janssen Research & Development, L.L.C., a Johnson & Johnson company, is recruiting for a Manager, Global CMC Regulatory Affairs - to be based in Titusville, NJ, Raritan, NJ, Spring House, PA or LaJolla, CA. Janssen Research & Development, LLC discovers and develops innovative medical solutions to address important unmet medical needs in oncology, immunology, neuroscience, infectious diseases and vaccines, and cardiovascular and metabolic diseases. Please visit http://www.JanssenRnD.com for more information. Janssen Pharmaceuticals, Inc. provides medicines for an array of health concerns in … (see more)
Regulatory Affairs Project Manager
Abbott - California
At Abbott, we're committed to helping you live your best possible life through the power of health. For more than 125 years, we've brought new products and technologies to the world -- in nutrition, diagnostics, medical devices and branded generic pharmaceuticals -- that create more possibilities for more people at all stages of life. Today, 94,000 of us are working to help people live not just longer, but better, in the more than 150 countries we serve. Please note that candidates need to be eligible to work in the U.S. without Abbott sponsorship. This position leads project submissions for … (see more)

Senior Regulatory Affairs Project Manager - Tustin
Advanced Clinical - California
Overview Our client needs a Senior Regulatory Affairs Project Manager who sees the world differently. Were looking for professionals with 7+ years experience in the medical device industry, who dont see obstacles but opportunity when it comes to assisting people to lead better lives. The Senior Regulatory Affairs Project Manager position is full-time, and is located in Irvine, CA. Were looking for problem solvers, innovators and those inspired by the work we do in making a difference today and with future generations. Responsibilities Serves as a member on project teams. Identifies regulatory … (see more)
Quality & Regulatory Affairs Manager - Trans Med (12379) - D
City of Hope - California
Job Description About City of Hope City of Hope, an innovative biomedical research, treatment and educational institution with over 5,000 employees, is dedicated to the prevention and cure of cancer and other life-threatening diseases and guided by a compassionate, patient-centered philosophy. Founded in 1913 and headquartered in Duarte, California, City of Hope is a remarkable non-profit institution, where compassion and advanced care go hand-in-hand with excellence in clinical and scientific research. City of Hope is a National Cancer Institute designated Comprehensive Cancer Center … (see more)
310 Regulatory Affairs Manager
Netsource, Inc. - Oakland/East Bay, California
Legal / Law Related
Skills: BS Degree, FDA Regulator Experience, Medical Devices Industry. FDA Experience. ISO/ 3485. 21CFR Part II Please note that this is a permanent position. This position is responsible for supporting sites manufacturing Medical Devices and or Medical Components which is part of the Commercial Strategice Business Unit. The support include providing guidance and oversight on Quality Management System development and implementation in compliance with applicable FDA QSR (21 CFR part 820), ISO13485, ISO 14971, IEC60601-1 and any other applicable ISO standards and global Medical Device … (see more)
Quality & Regulatory Compliance Coordinator
NorthBay Healthcare - Marin County/North Bay, California
Accounting / Finance
Job Description req2226 Quality & Regulatory Compliance Coordinator Full Time, FTE: 1 NorthBay Medical Center Fairfield, CA The Quality & Regulatory Compliance (QRC) Coordinator is responsible for hospital facility operations quality and regulatory compliance monitoring program management, ensuring that NorthBay Healthcare's facilities Compliance Management Program (CMP) is in a continuous state of readiness for inspection by any Authority Having Jurisdiction, including CMS, The Joint Commission, OSHPD and CDPH. The QRC Coordinator works collaboratively with facilities … (see more)
Applications Architect (Regulatory Programs)
MemorialCare Health System - California
Healthcare / Nursing
Applications Architect (Regulatory Programs) - (MEM002131) Description The Applications Architect independently provides specific systems consulting, systems analysis, and overall leadership related to the acquisition, coordination, integration, and use of complex, enterprise computing systems throughout MHS entities. Applies expert level knowledge of Meaningful Use (MU), or regulatory programs affecting healthcare information technology, to provide leadership, guidance, and coordination of technological optimization of the electronic health record (EHR). Applies in-depth knowledge of … (see more)
Displaying 1-10 of 1000 results

* The accuracy of search results can be improved by using quote marks around phrases.

Register for FREE!