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The Travel Oncology Registered Nurse (RN) provides specialized cancer patient care on a temporary basis in Saint Helena, California.. The role involves working 36 hours per week in 12-hour day shifts for a 13-week duration, delivering high-quality oncology nursing services.. PRIDE Health is seeking a travel nurse RN Oncology for a travel nursing job in Saint Helena, California.. PRIDE Health is the minority-owned healthcare recruitment division of Pride Global—an integrated human capital solutions and advisory firm.. Travel Nurse, Oncology Nursing, Registered Nurse, Cancer Care, Healthcare Recruitment, Temporary Nursing Job, Patient Care, Travel Healthcare, Nursing Benefits, Healthcare Staffing
Software Quality Assurance Analyst(s) Company: Inspirisys Solutions North America, Inc.. Limited domestic travel and/or occasional relocation to various u
The ideal candidate will have a strong background in testing cloud, mobile and web development, and will work closely with the engineering team and product management teams to create and execute on the companys roadmap. Agile Process : Able to work with software development projects using SCRUM techniques with 1-2 week Sprint cycles.. Managing Hybrid Remote Teams : Managing and improving teams will be a prime focus.. Driving Test Processes: Familiarity with modern testing methodologies including mobile, web and cloud automation.. Strong knowledge of QA test tools and processes
Design, develop, automate and execute test cases for front end and backend features for our Balloon.com product. Experience with tools such as SOAPUI, JMeter, Grinder or Selenium. Experience with using CI tools such as Jenkins and Bamboo. A Bachelor's degree in Computer Science, Electrical Engineering, Computer Information Systems or an equivalent combination of formal education and directly related experience, is required. Django is a registered trademark of the Django Software Foundation |DjangoJobs is not associated with the Django Software Foundation
Our international business services provide molecular insights to the top 10 MNC BioPharma’s to support biomarker-driven clinical trials in US, EU, APAC including China.. We are seeking a strategic and experienced Chief Commercial Officer (CCO) / VP of Sales with a robust background in healthcare to lead our commercialization efforts.. Develop and support tailored business strategies for early and growth-stage companies in precision medicine, biopharma, and life sciences.. Demonstrated success in developing tailored business strategies for early and growth-stage companies in precision medicine and biopharma.. Covenant House California: Chief Executive OfficerAPPLY BY: July 11, 2025 Chief Executive Officer at The Cultural Conservancy San Francisco Bay Area $175,000.00-$200,000.00 3 weeks ago
Axolabs specialises in a new class of drugs whose active ingredients are chemically derived from DNA or RNA. They are called oligonucleotide or nucleic acid therapeutics. In this role, you will support the Quality Assurance function at our brand new therapeutic GMP oligonucleotide facility. Quality Systems: Coordinate key quality processes including Change Control, Audits, CAPAs, QA holds, Material Rejection Reports, Deviations, QMS, Technical Complaints, and QA reporting. A 4-year college degree in Engineering, Chemistry, Biochemistry, Biological Sciences, or a related field, or an equivalent combination of education, training, and industry experience. Experience in CAPA, Deviation and Nonconformance reporting, internal auditing, and supplier management.
One of our missions at Agilent is to enable our customers to make new discoveries in the genomics field by providing array-based and Next Generation Sequencing workflow products as well as to gain genetic insights that can be used for pre- and postnatal diagnosis. Drive quality compliance projects and continuous improvement activities such as Kaizen, PDCA and Six Sigma.. Bachelor's in scientific fields (molecular biology, biochemistry, chemistry) or engineering (chemical engineering, bioengineering).. Agilent Technologies, Inc. is an Equal Employment Opportunity and Affirmative Action employer. Agilent Technologies, Inc., is committed to diversity in the workplace and strives to support candidates with disabilities.
At Everlane, we believe luxury should be as effortless as it is conscious.. We are looking for a Quality Control Associate to join our QA function of the Sourcing team at Everlane.. Implement and execute Everlane's global inspection and testing program in partnership with factories, third-party partners, and cross-functional teams. California Residents: At Everlane, we carefully consider a wide range of compensation factors, including your background and experience.. Everlane is deeply committed to respecting and protecting your data privacy.
The Sr. Director, GMP Quality Assurance is responsible for providing leadership, direction, and Quality Assurance (QA) oversight of contract manufacturers (CMOs) and service providers for drug substance (DS), drug product (DP), packaging and labeling, and distribution of multiple products.. The Sr. Director, GMP Quality Assurance provides QA expertise and guidance in supporting the development and product quality strategy for CMC teams and is responsible for execution of the day-to-day quality activities of CMO manufacturing, including but not limited to, disposition of all materials, deviation resolution, CAPA(s), change control(s), expiry/retest extension, product complaints and overall documentation supporting the suitability of batches.. The Sr. Director of GMP Quality Assurance is a fully remote role and will preferably be based on the US West Coast.. Serve as the QA lead for all GMP-related activities including supplier qualification, tech transfer, scale-up, manufacturing (DS, DP, FDP), and disposition of clinical materials.. At least 18 years of experience in GMP Quality Assurance at an operational level supporting manufacturing and quality control in a pharmaceutical or biotech environment.
Perform high-quality diagnostic X-ray examinations as directed by physicians.. Operate and maintain X-ray equipment, ensuring it is properly calibrated and functioning.. Follow established radiation safety standards and infection control guidelines.. Certification: ARRT (American Registry of Radiologic Technologists) certification in Radiography required.. Experience: A minimum of 1-2 years as a Radiologic Technologist, preferably in an outpatient or clinical environment.
Manage advanced clinical research studies for product development initiatives in the contact lens industry.. Be aware of basic regulatory requirements related to medical devices (GCP/IRB/Design Control/FDA & ISO standards/EU MDR, etc.). Understanding of biological and optical contributors to contact lens safety and performance.. Minimum 2 years’ experience in the contact lens or medical device industry.. Clinical or Research degree in Vision Science, Visual Optics, Physiological Optics, or Optometry/Ophthalmology highly preferred.
As the Technical Recruiter at Charta, you'll play a pivotal role in designing, implementing, and scaling our talent acquisition strategy to attract world-class team members.. As Charta Health’s first Technical Recruiter, you’ll partner with our Talent Lead to scale the engineering, data, and AI teams that power our product.. You’ll own full-cycle searches for critical technical roles, refine our recruiting toolkit, and help shape a best-in-class candidate experience, all within a fast-growing AI health-tech startup.. Growth opportunities in a fast-paced, innovative tech startup. Lively fully in-person (5 days per week)work culture at our headquarters in downtown San Francisco
We're seeking a Product Verification and Validation Engineer to join our medical devices compliance team, focusing on wearables and Software as a Medical Device (SaMD).. You will work on cutting-edge wearable technologies, including augmented reality glasses, wrist wearables, and other innovative devices.. Sensor validation: Working with advanced sensors, such as electrodermal activity (EDA) sensors, heart rate variability (HRV) sensors, and other physiological sensors.. Experience with Six Sigma tools (e.g. MSA, Gage R&R, ANOVA, DOE etc). Please note that Meta may leverage artificial intelligence and machine learning technologies in connection with applications for employment.
Reporting to the Clinic Director and in consultation with the Department Chair, the Clinical Services, the Support Specialist plays a pivotal role in the advancement of the Department of Audiology’s mission.. University of the Pacific recognizes that diversity, equity, and inclusion is foundational to the success of our valued students and employees.. We prioritize policy and decision-making that demonstrates awareness of, and responsiveness to, the ways socio-cultural forces related to race, gender, ability, sexuality, socio-economic status, etc.. Preferred Qualifications Certification in medical billing and coding or similar credentials.. Demonstrated experience in advancing social justice, equity, and inclusion in a university setting.
Within our portfolio of companies, International SOS, headquartered in Houston, Texas provides contracted healthcare support to Government defense and civil agencies and government contractors, including support to military exercises and operations, diplomatic missions, natural disasters, and refugee care.. The National Patient Safety Risk Manager (PSRM) provides management, expertise and oversight of a comprehensive quality, health, safety, and risk management program for the medical services contract and medical units of the U.S. Customs and Border Protection (CBP), U.S. Border Patrol Station Medical Units, and Office of Field Operations Ports of Entry Medical Units.. Contracted medical staff will be working alongside uniformed Customs and Border Protection (CBP) Agents/Officers in secured federal facilities along the southwest border of the United States.. CBP's Office of the Chief Medical Officer (OCMO) employs a trauma informed care model to provide frontline medical care for persons in CBP custody in accordance with Enhanced Medical Support Efforts CBP Directive (2210-004).. Serves as direct supervisor for the Electronic Health Records Specialist, providing administrative oversight, mid-term review, and annual performance evaluation, under the guidance and oversight of the NPSQMD.
The Clinical QA Director is responsible to ensure quality is embedded throughout the lifecycle of all the ongoing clinical programs through oversight, assessment and monitoring, risk assessment tools and risk mitigations.. Free access to Genentech Bus & Ferry Share program. Free onsite gym and a kitchen stocked with yummy snacks and drinks!. Neurodivergence, for example, attention-deficit/hyperactivity disorder (ADHD), autism spectrum disorder, dyslexia, dyspraxia, other learning disabilities. Traumatic brain injury
Axolabs specialises in a new class of drugs whose active ingredients are chemically derived from DNA or RNA. They are called oligonucleotide or nucleic acid therapeutics.. Join us at LGC as a Quality Assurance Specialist III - Therapeutics and be a part of our innovative team!. In this role, you will support the Quality Assurance function at our brand new therapeutic GMP oligonucleotide facility.. Quality Systems: Coordinate key quality processes including Change Control, Audits, CAPAs, QA holds, Material Rejection Reports, Deviations, QMS, Technical Complaints, and QA reporting.. Experience in CAPA, Deviation and Nonconformance reporting, internal auditing, and supplier management.