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StartDate: ASAP Available Shifts: 8 D Pay Rate: $1883.79 - $2064.15 Discover an exciting opportunity in Cupertino, CA, where the natural beauty of Rancho San Antonio County Park and the cultural allure of the Cupertino Cherry Blossom Festival await.. The skilled nursing facility is recognized with a 5-star Medicare Rating, ensuring you work within a highly respected environment committed to patient care excellence.. As an Occupational Therapist, you'll handle daily 8-hour shifts focusing on personalized therapeutic interventions that will support patient recovery and independence.. Embrace this fulfilling role in a community acclaimed for its innovation and scenic charm.. occupational therapist, occupational therapy, OT, therapist, patient care, healthcare, health care, skilled care, skilled occupational therapist, skilled care occupational therapist, skilled
We are one of the largest private duty nursing companies in the nation and growing!. Flexible scheduling- full-time, part-time, or PRN. Days, nights, and weekend shifts— we will work with your availability!. Weekly and/or Daily Pay. Our homecare is always delivered from a place of heartfelt compassion and empathy, and every one of our Licensed Vocational Nurses (LVN)s works together to make sure we achieve outstanding clinical outcomes.. As an employer accepting Medicare and Medicaid funds, employees must comply with all health-related requirements in all relevant jurisdictions, including required vaccinations and testing, subject to exemptions for medical or religious reasons as appropriate.
This unique opportunity is at a prestigious facility looking to hire a traveling therapist.. This exciting area offers many recreational activities.. As a premier travel therapy company, Host Healthcare offers top pay, excellent benefits, and personalized service.. The ideal candidate for this position will be dedicated to providing patients with the highest level of service.. The ideal candidate will also be knowledgeable in Medicare, Medicaid, and private insurance, as well as the ability to complete relevant insurance documentations.
Enterprise Medical Recruiting is partnering with a PACE program in Modesto, California, to hire a dedicated and compassionate Physician Assistant.. Comprehensive benefits package, including: Health insurance Loan Forgiveness Program (PSLF) HPSA area designation (Primary Care Score of 18) FTCA occurrence-based malpractice insurance Paid licensure/dues 403B matching program and defined pension plan contribution CME support and vacation time. The All-Inclusive Care for the Elderly (PACE) program supports seniors in receiving the care they need while living in their communities.. Individuals aged 55+ with Medicare or Medicaid (or both) who require a nursing home level of care but can safely live in the community with PACE support.. The program covers all necessary services, including provider visits, medications, home care, transportation, hospitalizations, and nursing home stays when required.
The Principal Regulatory Affairs Specialist provides regulatory leadership for product manufactured by PROCEPT BioRobotics (“company”) from development through marketing approval and commercialization. The initial role of the Principal Regulatory Affairs Specialist will be as an individual contributor, reports to the Senior Director of Global Regulatory Affairs. Knowledge of EU MDR regulations is required.. It starts with our live induction program that serves as an incubator for cross-functional team building, an immersion in Procept’s history, jam-packed interactive sessions with executive leadership and a crash-course in the mission and purpose of what we do. We offer a comprehensive benefits package that includes full medical coverage, wellness programs, on-site gym, a 401(k) plan with employer match, short-term and long-term disability coverage, basic life insurance, wellbeing benefits, flexible or paid time off, paid parental leave, paid holidays, and many more!
Hit Apply below to send your application for consideration Ensure that your CV is up to date, and that you have read the job specs first.. Pulmonx is looking for a Sr Regulatory Affairs Specialist to join our team supporting all regulatory aspects of our groundbreaking medical devices.. If you enjoy a mix of both tactical and strategic hands-on work with a strong group of Regulatory Affairs experts, please apply!. Stay current with industry trends and best practices in international regulatory affairs.. Minimum of 3-5 years of experience in regulatory affairs, specifically with Class II or Class III medical devices.
Director of Regulatory Affairs (San Francisco, CA). Oversee the preparation, review, and submission of regulatory documents, including INDs and FDA submissions.. Guide project teams in interpreting and communicating regulatory requirements.. Education: BA/BS degree in biological or physical sciences preferred.. Proficient in MS Office and experience with document management systems.
Their reach is global and they are the industry leader in their specialty, with a second location in Asia. The investment into R&D is significant with several products in the pipeline at various stages and their financial standings are strong.. The Principal Regulatory Affairs Specialist hired will report to the Senior Director of Regulatory and Quality, with sights to build out an RA team as needed.. Assess regulatory impact of post-market changes on labeling, design, materials, manufacturing process, sterilization, or packaging and notify regulatory agencies and NB of substantial changes.. 5-10 years experience in regulatory affairs within the medical device industry. Authoring experience in FDA product submissions (IDE, PMA, 510k)
We are passionate about advancing scientific discoveries to become important medicines for rare disease patients. The Associate Director, Global Regulatory Affairs provides management of all aspects of assigned regulatory activities for the dedicated regions and related to the development and commercialization of novel liver drugs including quality, preclinical and clinical areas of drug development. The role is responsible for ensuring full regional regulatory compliance, and overseeing submissions and approvals of regulatory procedures including but not limited to IND, NDA, MAA. Strong understanding of US FDA, EU and international pharmaceutical guidance, regulations, drug development process, and industry standard practices. Experience with regulatory submissions (e.g. New Drug Applications (NDA/NDS/MAA), post marketing measures, Paediatric Investigation Plans (PIP) and Orphan Drug Designation (ODD) activities).
With more than 30 ongoing studies across a wide range of disease areas, including endocrinology, oncology, metabolism, and neurology, we remain dedicated to advancing the possibilities of cortisol modulation.. What began as a ripple of scientific truth is now poised to unleash a sea change of discovery representing a fundamental shift in the way we understand and treat disease.. Proficiency in use of MS Office applications (Word, Outlook, Excel, Powerpoint), Adobe Acrobat, electronic document management systems (eg, Veeva Vault, Box, SharePoint), and templates (eg, StartingPoint). BA/BS degree in a scientific field required; advanced scientific degree (PhD, PharmD, or MS) preferred. Knowledge of endocrinology, oncology, neurology and/or metabolic disease areas preferred
Sr Regulatory Affairs Specialist (Ad/Promo) (Remote) - Shockwave.. Senior Regulatory Affairs Specialist -Vascular (on-site).. Senior Regulatory Affairs Specialist – Vascular (on-site).. Regulatory Affairs Manager – Heart Failure (on-site).. Regulatory Affairs Manager – Vascular (on-site)
We are partnering with a well established Biotech company here in the SF Bay Area as they search for their next Associate Director of Regulatory Affairs. Oversee the planning, preparation, and submission of regulatory documents to global health authorities (e.g., FDA, EMA), including INDs, CTAs, DMFs, BLAs, and MAAs. Partner with regulatory operations to build and maintain submission timelines and global regulatory plans. Bachelors degree in Life or Health Sciences required; advanced degree (MS, PhD, PharmD) strongly preferred. 810 years of industry experience in pharmaceuticals or biotechnology, with a minimum of 46 years in regulatory affairs.
Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report.. This position will be responsible for supporting the maintenance of the Global Regulatory Affairs filing system and the Registration Tracking System (RTS) database.. Maintain the Global Regulatory Affairs filing system including the filing of submissions and correspondence both electronically and hard copy. Maintain the RTS database to ensure submission, regulation updates, and correspondence data is accurately entered in a timely manner. Can effectively and efficiently organize Regulatory Affairs documentation to ensure accurate filing and timely retrieval of documents, can multi-task workload to ensure tasks are completed in a timely manner, knowledge of database systems to ensure information is accurately entered and easily retrievable.
We pride ourselves on a collaborative workplace culture, offering fully remote roles, regular opportunities to connect with team members, and meaningful work.. We accept Medicaid, Medi-Cal, Medicare, and Commercial insurance, allowing us to serve a diverse range of patients.. Must be comfortable using computers and video-conferencing software; previous telemedicine experience is a plus.. Qualifications and skills Unrestricted independent license (LMFT, LCSW, LMHC or LPC) in good standing. Are you interested in providing affordable mental health care to Medi-Cal, Medicaid, or Medicare clients at a rate of $70 per hour?
Oversee the SNF's infection control, employee health, staff development, and Minimum Data Set (MDS) processes.. Bachelor's Degree in Nursing or 4 Years job experience as long term care, geriatric and/or rehabilitative nurse with specialization in the field of work in a Skilled Nursing Facility. 3 Years job experience as long term care, geriatric and/or rehabilitative nurse with specialization in the field of work in a Skilled Nursing Facility. Industries Non-profit Organizations. RN Manager, Care Management - Case Management RN, Nurse Lead, Part Time, Cardiac Rehab, Saint Helena We’re unlocking community knowledge in a new way.
We are home to a regional Center of Excellence for Leukemia and Lymphoma, with a robust clinical trial portfolio, including enrollment of patients on national clinical trials (SWOG, ECOG, NRG, NCI).. Opportunities to participate in and be part of a sub-specialty regional hematology group, clinical trial enrollment (SWOG, ECOG, NRG, NCI), teaching, and Commission on Cancer Accredited team who focuses on state-of-the-art personalized cancer care.. Clinical experience in both benign and malignant hematology, sickle cell, hemophilia, and solid tumors of all types, including brain tumors. FOR ADULT OPPORTUNITIES, you may also contact Bo Chau at: Bo. Chau@kp.org or call 510-418-9952.. FOR PEDIATRIC OPPORTUNITIES, you may also contact Judy Padilla at: Judy. G.Padilla@kp.org or call: 510-368-4513.
Our employees are our greatest asset as we work to achieve our bold ambitions, and we’re looking for the next wave of passionate and ambitious people ready to make a direct impact.. PharmD/PhD with 8+ years’ experience in the biopharma industry, including extensive experience working in regulatory or a related discipline OR. Extensive experience participating in cross-functional projects and teams with responsibilities related to clinical trials or other drug development activities.. Significant experience participating in cross-functional projects and teams with responsibilities related to clinical trials or other drug development activities.. Similar Jobs (5) Director, CMC Regulatory Affairs – Biologics locations United States - California - Foster City time type Full time posted on Posted 30+ Days Ago Executive Director, Global Clinical Supply Chain - Oncology locations United States - California - Foster City time type Full time posted on Posted 30+ Days Ago Executive Director, Global Head of Medical Affairs Technology locations 2 Locations time type Full time posted on Posted 30+ Days Ago
Nurse Coordinator: Previous RNC (nurse coordination) and Epic experience required.. Inpatient ICU, MedSurg, or Endoscopy experience is necessary due to high triage volume for the GI center.. Facility Location: Known as the "Birthplace of Silicon Valley" and home to Stanford University, Palo Alto offers a blend of tradition and innovation.. Located 35 miles south of San Francisco, this college town features a charming downtown, parks, cultural offerings, and excellent travel nursing opportunities.. About the Company: At AMN Healthcare, we aim to be the most trusted, innovative, and influential partner in helping healthcare organizations deliver quality patient care that evolves to be more human, effective, and achievable.
One of California's most highly respected senior living communities is seeking a dedicated and experienced Director of Nursing to join their leadership team.. We're looking for a Director of Nursing with proven leadership experience in senior living or hospital settings who is ready to take their career to the next level.. Career scholarships & continuing education support. Clinical Nursing Director - Perioperative Services RN - Executive Director - Surgical Services - Nursing Administration - CMC - Full Time - 8 hour - Days Concord, CA $236,204.00-$354,306.00 2 weeks ago. Health Service Director- LVN- Sign on bonus offered!
As an AE, you will be responsible for owning the full sales cycle for mid-market and growth accounts, with a focus on building relationships across Quality, Regulatory Affairs, and Post-Market Surveillance teams. You’re a consultative seller with deep curiosity about your customer’s business and a track record of success in complex sales environments. Top pharmaceutical companies, food manufacturers, medtech companies, and service firms from around the globe rely on Redica Systems to mine and process government inspection, enforcement, and registration data. This enables them to quantify risk signals from their suppliers, identify market opportunities, benchmark against peers, and prepare for the latest inspection trends. Our data and analytics have been cited by major media outlets including MSNBC, The Wall Street Journal (WSJ), and The Boston Globe.