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Preferred Healthcare Staffing is seeking a travel Skilled Nursing Facility (SNF) Occupational Therapist for a travel job in San Francisco, California.. Occupational Therapist (OT) - Skilled Nursing Facility. We are looking for a talented Occupational Therapist with skilled nursing experience to work at an excellent healthcare facility in San Francisco, California.. This is a fantastic opportunity to build upon your occupational therapy skills while advancing your OT career.. We pride ourselves on honesty, building lasting relationships, and genuinely taking care of our HCPs. We believe this helps to achieve our mutual goal: better patient care.
Provides continuous availability for medical and technical questions to our client patients, our patient care staff, and ancillary care providers.. Adheres to privacy, compliance, and quality programs and other regulatory and compliance standards of the Practice and the Crossover Medical Group.. Completion of an ACGME approved Residency in Family Medicine or Internal Medicine. Current Certification or active participation in the exam process leading to certification by a Family Medicine or Internal Medicine Specialty Board.. Knowledge of and experience with managed healthcare systems including, quality assurance, quality improvement, risk management, and population health and disease management programs
CAPA management, including investigation, documentation, and timely closure of exception reports.. Post-market surveillance data coordination and reporting.. OUS/ Redline procedures/ Report ability/ experience/ CAPA. Post Market Surveillance experience is as plus/ Analyst work. Experience in ensuring compliance with Quality Management Systems, including complaints coordination, batch release, exception reports, CAPA, document control, surveillance, testing, batch and sample retention, and metric maintenance.
Interim HealthCare offers online courses and training to help build your skills, gain specializations and earn CEUs. And, if your goal is to become a nurse or other healthcare professional, we will support you with tuition discounts that pave the way forward.. Leaders in our industry, Interim HealthCare is hiring Home Health CNAs who are committed to providing exceptional patient care and eager to grow in their career.. Help with daily activities such as bathing, toileting, dressing, grooming, hygiene, nail/skin care, eating and nutritional intake. Founded in 1966, Interim HealthCare is the nation’s first home care company and a leading employer of Certified Nursing Assistants (CNAs).. Interim HealthCare is an equal opportunity employer that is committed to diversity and inclusion in the workplace.
These characteristics have allowed us to forge strong, authentic bonds with the caregivers, patients, health care professionals (HCPs) and community members we serve.. Provide regulatory advice and information to cross-functional teams and to other functional areas (i.e., CMC, nonclinical, and clinical) for product development and planning to support the timely achievement of company and department goals.. A degree in a life science or closely related discipline with a higher degree preferred (e.g., MSc, MPH, PhD, PharmD).. A minimum of 15 years direct pharmaceutical regulatory affairs, including 5 years of International Regulatory experience is required.. Experience in a small company and hands-on marketing application experience from preparation through submission and approval in a non-oncology, rare disease indication is strongly preferred in regions including, but not limited to EU, APAC, and LATAM.
Process and Organizational Effectiveness.. Take personal responsibility for the Notification of Regulatory activities and related database entry/data accuracy for allocated projects. At least three-year experience working in a medical device manufacturing company, preferably with capital medical equipment, highly desired. AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion. It is AbbVie's policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.
Will also be responsible for resolving orders via the EA (External Adjudication) queue.. Determines if prescription requires physician clarification or if it should be forwarded to therapeutic intervention or doctor phone calls for follow-up.. Assists in patient services as required, taking incoming prescription medication questions/concerns from patients.. Assists in the doctor phone call area and/or therapeutic intervention as assigned and contacts physicians to resolve any questions or concerns.. Maintains established procedures concerning quality assurance, security of controlled substances, and disposal of hazardous waste drugs.
Perform data review supported by Clinical Research Scientist(s) (CRS), participate in protocol deviation meeting that will occur monthly or as needed.. Create or support the creation of relevant clinical documents of high quality, such as study protocol protocol(s), investigator brochure (IB), informed consent forms (ICF), case report forms (CRF), Clinical study report (CSR), NDA/MAA registration documents, and scientific publications.. Successful completion of MD training mandatory; 3 years of clinical experience in treating oncology patients or a completed fellowship in a Hematology-Oncology program.. 8 years of combined experience in oncology clinical research and drug development in academic and/or industry, including experience as a medical monitor and (sub)investigator in oncology clinical trials.. 3 years in industry leadership as medical lead for an oncology development program(s) with direct or indirect management of cross-functional areas (e.g., clinical operations, biostatistics, data management, biomarker, pharmacovigilance, quality, etc.)
Lead the development and review of key documents, including statistical analysis plans, clinical study reports, and regulatory filings (e.g., NDA, BLA, MAA).. Ensure compliance with industry and regulatory standards, including ICH, GCP, FDA, EMA, and CDISC.. Strong knowledge of statistical methods for clinical trials, regulatory guidelines, and CDISC standards (SDTM, ADaM).. Director of Finance and Administration, Biomedical Data Science. Director, Early Clinical Development (MD), Autoimmune Cell Therapy
The Associate Director of CMC Regulatory Affairs provides support for all CMC regulatory activities related to the ongoing development, registration, and life-cycle management of RYTELO (imetelstat) and other potential future development product candidates.. The position is remote with a corporate headquarters in Foster City, CA and Parsippany, NJ. The Associate Director reports to the Senior Director, CMC Regulatory Affairs.. Support other US/EU/labeling and operations groups within global Regulatory Affairs on behalf of CMC regulatory as needed. Provide review and input on updates to CMC regulatory documents (e.g., QOS/Module 3) for submission to regional regulatory agencies and contribute to preparation of registration dossiers (e.g., NDA and MAA). Breadth of global CMC regulatory affairs experience in drug development and for commercialized products is required with a good all-round understanding of Module 3 content and requirements
The technologist is licensed in all scopes of practice as defined by the State of California Radiologic Health branch, and performs routine to complex diagnostic and therapeutic nuclear medicine procedures using radiopharmaceuticals to assist in diagnosis and/or treatment in both the inpatient and outpatient environment.. Responsible for performing radiation safety and quality control procedures on all Nuclear Medicine equipment as required by the department.. Oversee advanced nuclear medicine fusion imaging procedures to ensure diagnostic precision and optimal patient care.. Possession of a valid Nuclear Medicine Technologist certification and state licensure is required.. Extensive experience with fusion imaging modalities, including PET/CT and SPECT/CT, is preferred.
Arcellx is a public, clinical-stage biotechnology company reimagining cell therapy by engineering innovative immunotherapies for patients with cancer and other incurable diseases.. Maintain detailed knowledge of global regulatory environment relevant for cell therapies and regenerative medicine.. Join us in our quest to reimagine cell therapy and destroy cancer.. Director, CMC Regulatory Affairs Biologics. Clinical Research Regulatory Affairs Manager
This position is responsible for the management, operation, and upkeep of the Quality Assurance activities and support Inspection readiness activities for GxP (GMP, GLP, & GCP) programs.. ESSENTIAL DUTIES AND RESPONSIBILITIES: Perform quality oversight of cGMP activities which include independently setting up and/or optimizing processes for, drug substance and drug product manufacturing, labeling, batch record review and lot disposition. as needed for consistency with applicable regulations and for compliance with company's GMP Quality System. Identify and support continuous improvement projects in collaboration with CMC, QC and RA to achieve quality, reliability and efficiency improvement objectives. Provide quality assurance support in the technology transfer, scale-up, validation and manufacturing at CMO.
The Ceribell System is a novel, point-of-care electroencephalography ("EEG") platform specifically designed to address the unmet needs of patients in the acute care setting, and is being used in hundreds of community hospitals, large academic facilities and major IDN's across the country.. This role will also assist on maintaining quality systems, supporting Corrective and Preventive Actions (CAPA), Non-conformance Reports (NCR), complaints, audits, and overall Quality Management System (QMS) functions.. Participate in design control activities to ensure software quality throughout the product lifecycle, including planning, development, testing, and post-market surveillance.. Bachelor's degree in Computer Science, Biomedical Engineering, Electrical Engineering, Quality Engineering, or a related technical field (Master's ), or equivalent experience.. Certification in quality management or software quality (e.g., ASQ, CMMI) is a plus.
Primary responsibilities include executing test plans, updating test reports, debugging and writing defect reports, verifying fixes, developing test automation scripts, and building automation solutions.. Experience with automation scripts using tools like Selenium WebDriver, Appium, Protractor, Mocha, Jasmine, and TestNG. Good understanding of web technologies including HTML, CSS, XML, JSON, and RESTAPIs. Good knowledge of modern front-end frameworks such as Vue.js, React, Angular. Experience with databases, API, backend systems, and mobile testing (iOS/Android)
Kforce has an enterprise client that is seeking a Quality Assurance Tech in Sunnyvale, CA. We are seeking a talented and highly motivated Quality Assurance Engineer (QAE) for a contract position. Experience with HTML, JavaScript, Java and SQL is desired but not required.. The pay range is the lowest to highest compensation we reasonably in good faith believe we would pay at posting for this role. We offer comprehensive benefits including medical/dental/vision insurance, HSA, FSA, 401(k), and life, disability & ADD insurance to eligible employees.
Produce Facility Monitoring reports, Unannounced Visit reports, Quality Assurance Reviews, Corrective Action Plans, Immediate Danger Reports, Sanctions, and correspondence, and file material as needed.. Coordinate with SARC case management, SARC BCBA team, SARC Health Services Unit to arrange and facilitate EBSH, CCH, and ARFPSHN Quality Assurance Reviews.. Coordinate with DDS and lead any reviews with DDS for EBSH/CCH and FHA. Attend and provide support for relevant meetings, including Mortality, Let’s Talk, Quality Assurance Advisory, Residential and Day program round table, etc.. Standards Compliance Coordinator
Perform visual and dimensional/mechanical inspection of raw materials such as, machined parts, optics, chassis, assemblies, packaging materials (labels, software, product inserts, optics, etc. Follow BDIS Environmental, Health and Safety (EH&S) policies and procedures. Computer literate with basic knowledge or Microsoft Windows & Office, SAP, Minitab, etc. Staff Software Quality Assurance Engineer Quality Assurance Quality Control Engineer Commercial Kitchen Equipment and Refrigeration Technician San Francisco Bay Area $130,000.00-$165,000.00 2 weeks ago.. Process Validation Engineer (Manufacturing Processes and QC Test Methods) Technician II Quality Control - First Shift We’re unlocking community knowledge in a new way.
Minimum of 3-5 years practical experience in a quality, laboratory or cGMP regulated production environment in 21 CFR regulated industries (i.e., food, dietary supplements, personal care, medical devices, etc.. Familiarity / knowledge of cGMPs, HACCP/food safety, laboratory safety, GFSI/SQF, ISO, National Organic Program and Kosher guidelines a plus. An innovative leader in the organic food industry, Nutiva (www. nutiva.com) is the world's best-selling brand of organic coconut, hemp, chia and redpalm superfoods. We donate 1% of sales to support sustainable agriculture.
Experience with biologics, tissue/organ or cord blood/stem cells or equivalent. Autoimmune disorder, for example, lupus, fibromyalgia, rheumatoid arthritis, HIV/AIDS. Neurodivergence, for example, attention-deficit/hyperactivity disorder (ADHD), autism spectrum disorder, dyslexia, dyspraxia, other learning disabilities. Pulmonary or respiratory conditions, for example, tuberculosis, asthma, emphysema. Traumatic brain injury