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Requirements: ARRT Preferred Basic Life Support Current State License 1-2 years experience is required To provide radiation therapy treatment to patients prescribed by the Radiation Oncologist for the treatment of cancer patients, must be Radiation Therapy certified (RRT).. Experience on various Radiation Therapy equipment including Varian, GE, TOMO, etc.. Responsibilities: A Radiation Therapist provides radiation oncology treatments, radiation oncology treatment preparation, including simulation, medical intake, treatment planning preparation and quality assurance activities.. Works with radiation oncologist on simulation treatment schedule and performs simulations.. Delivers radiation treatments per radiation oncologist orders.
MedPro Healthcare Staffing , a Joint Commission-certified staffing agency, is seeking a quality Cath Lab Technologist for a contract with one of our top healthcare clients.. Assists in the performance of various invasive cardiac or peripheral vascular diagnostic and therapeutic procedures.. Functions under the direction and immediate supervision of the cardiologist/radiologist performing the procedure.. Assists cardiologist during procedures by operating ancillary equipment, anticipating and obtaining catheters, wires and other necessary inventory and medications as ordered.. Key Words: Cath Lab Technologist, EKG Tech, Electrocardiograph Tech *Weekly payment estimates are intended for informational purposes only and include a gross estimate of hourly wages and reimbursements for meal, incidental, and housing expenses.
Software Quality Assurance Analyst(s) Company: Inspirisys Solutions North America, Inc.. Limited domestic travel and/or occasional relocation to various u
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
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
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow.. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio.. For more information about AbbVie, please visit us atwww.. abbvie.com. Follow @abbvie onX,Facebook,Instagram,YouTube,LinkedInandTik Tok.. AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.
The Registered Nurse (RN) provides patient-centered care through the nursing process of assessment, diagnosis, planning, implementation, and evaluation.. Participates in performance improvement initiatives, including data collection and process development, to enhance patient outcomes and care delivery.. Emergency Services RN: Provides immediate and critical care to patients with urgent medical needs.. Assists in trauma procedures (chest tube insertion, peritoneal lavage).. To apply, please email jordan_mangas@chs.net
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.
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.
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.
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.
Job Title: Clinical Outcomes and Utilization Management Nurse. We are currently hiring a Clinical Outcomes and Utilization Management Nurse to work onsite in our San Francisco, CA office.. 35 years of clinical experience in home health, quality review, or care management. Experience in utilization review, quality assurance, or regulatory compliance strongly preferred. MondayFriday schedule (no weekends or field work)
The company aims to leverage cutting-edge biological research to create breakthrough medicines addressing high unmet needs across multiple therapeutic areas, including neurology, pulmonology, cardiology, nephrology, and endocrinology.. Founded in 2015, the company has built a portfolio of 20+ drug development programs ranging from preclinical to late-stage development in multiple therapeutic areas including genetic dermatology, precision oncology, cardiology, endocrinology, neurology, pulmonology, and renal disease, with two approved drugs.. Collaborate with (and serve as a clinical/medical resource) for cross-functional colleagues (clinical operations, statistics, regulatory affairs, CMC team, medical affairs, etc. Help ensure Clinical Study Team compliance with FDA, EMEA, ICH, and GCP guidelines and internal SOPs.. Experience in rare disease fields and/or dermatology, hepatology, or non-malignant hematology is a plus.
The Pharmaceutical Sales Rep Professional will act as the primary customer contact for demand creation by marketing pharmaceutical products to physicians.. Specifically, the Pharmaceutical Sales Rep is responsible for promoting healthcare products per the laws, regulations, and company policies governing the promotion of the healthcare product.. Each Pharmaceutical Sales Rep has an assigned territory and reports to a Sales Manager.. In this strategic sales role, the Pharmaceutical Sales Rep provides current and comprehensive clinical knowledge of pharmacology products to customers and effectively communicates the clinical and economic benefits of the pharmacology product in accordance with approved promotional labeling.. Each Pharmaceutical Sales Rep is also responsible for collaborating with other field-based team members/Account Managers responsible for servicing and educating the target customer and their practice.
Licensed Vocational Nurse (LVN). Pioneers in our industry, Interim HealthCare Staffing is an employer of choice to LVNs nationwide.. Take patient vitals, do assessments, document progress and report changes to RN supervisor. Founded in 1966, Interim HealthCare Staffing is the nation’s first healthcare staffing company and a leading employer of Licensed Vocational Nurses (LVNs).. Join a nationwide network of LVNs who have discovered the balance and fulfillment that healthcare staffing brings.
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.
Vituity is seeking a Board Eligible / Certified Internal Medicine physician to join as a Reservist Hospitalist Medical Director in a flexible travel role across the nation.. Opportunities to attend Diversity, Equity and Inclusion events including LGBTQ+ History, Dia de los Muertos Celebration, Money Management / Money Relationship, and more.. Superior Health Plan Options. Diversity, Equity and Inclusion (DEI) initiatives including LGBTQ+ History, Dia de los Muertos Celebration, Money Management / Money Relationship, and more.. Hospitalist, Medical Director, Internal Medicine, Vituity, Physician Partnership, Telemedicine, Travel Physician, Patient Care, Healthcare Innovation, Diversity and Inclusion
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.