UNKNOWN

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We are comprised of a 221-bed hospital, 21 physician clinics, home care services, comprehensive cancer care and a vast scope of award-winning services located throughout Marysville and the surrounding areas. Positions and instructs patients prior to examination, adjusts the x-ray equipment and determines proper voltage as well as current and desired exposure time for each radiograph.

Centered in the heart of Yuba-Sutter County, Adventist Health and Rideout has been one of the area's leading healthcare providers since 1907. We are comprised of a 221-bed hospital, 21 physician clinics, home care services, comprehensive cancer care and a vast scope of award-winning services located throughout Marysville and the surrounding areas. The allure of Marysville's community is complimented by its proximity to major metropolitan cities in the Bay Area and Sacramento, as well as just a quick drive to Lake Tahoe.Job Summary:Operates x-ray equipment to produce radiographs of designated portions of body as ordered by physicians. Positions and instructs patients prior to examination, adjusts the x-ray equipment and determines proper voltage as well as current and desired exposure time for each radiograph.Job Requirements:Education and Work Experience:<ul><li>Associate's Degree in radiological technology: Preferred</li></ul>Licenses/Certifications:<ul><li>American Registry of Radiologic Technologists \u2013 Radiography (ARRT-R): Required</li><li>Radiologic Tech (RT) in the state of practice: Required in CA and HI</li><li>Basic Life Support (BLS OR HS-BLS OR RQIBLS) certification: Required</li><li>Fluoroscopy license in state of employment: Required in CA within 6 months of hire</li></ul>Facility Specific License/Certifications:<ul><li>Fluoroscopy (FLUORO): Required</li></ul>Essential Functions:<ul><li>Performs screening procedures for diagnostic interpretation. Explains procedures to patients and answers questions. Prepares equipment for use as needed. Prepares examination rooms for patient exams. Positions patients for imaging exams. Monitors patients and ensures safety during exams.</li><li>Produces diagnostic images. Documents exam information. Reports important information to the physician.</li><li>Verifies exams on PACS.</li><li>Performs other job-related duties as assigned.</li></ul>Organizational Requirements:Adventist Health is committed to the safety and wellbeing of our associates and patients. Therefore, we require that all associates receive all required vaccinations as a condition of employment and annually thereafter, where applicable. Medical and religious exemptions may apply.Adventist Health participates in E-Verify. Visit <a href="https://adventisthealth.org/careers/everify/" rel="nofollow">https://adventisthealth.org/careers/everify/</a> for more information about E-Verify. By choosing to apply, you acknowledge that you have accessed and read the E-Verify Participation and Right to Work notices and understand the contents therein.

Mid-Columbia Medical Center

Radiologic Technologist - Full Time - Weekends Only - Day Shift

Cancer

Healthcare Providers

Home Care

Hospital

Patient Education

Picture Archiving and Communication System (PACS)

Radiography

Radiology

Essential Functions: Completes clinical reviews of acute medical patients using the Optum/Inter Qual tool to determine if the patient is in the right acute setting, receiving the right acute services, during the appropriate length of stay. Reviews patient medical records, assessing the appropriateness and necessity of proposed treatments, and collaborating with healthcare providers and insurance companies to ensure a seamless care experience and the practicing of financial stewardship and denial prevention.

Located in the metropolitan area of Sacramento, the Adventist Health corporate headquarters have been based in Roseville, California, for more than 40 years. In 2019, we unveiled our WELL-certified campus - a rejuvenating place for associates systemwide to collaborate, innovate and connect.Whether virtual or on campus, Adventist Health Roseville and shared service teams have access to enjoy a welcoming space designed to promote well-being and inspire your best work.Preferred candidate will be based in Roseville, CA, Glendale, CA or Portland, ORJob Summary:Plays a critical role in ensuring that patients receive high-quality care while efficiently utilizing medical resources. Reviews patient medical records, assessing the appropriateness and necessity of proposed treatments, and collaborating with healthcare providers and insurance companies to ensure a seamless care experience and the practicing of financial stewardship and denial prevention. Focuses on maximizing patient outcomes and optimizing resource allocation. Utilizes exceptional clinical knowledge, excellent communication skills, and the ability to thrive in a fast-paced and ever-changing healthcare environment.Job Requirements:Education and Work Experience:<ul><li>Associate's Degree in nursing or equivalent combination of education/related experience: Required</li><li>Bachelor's Degree in Nursing (BSN): Preferred</li><li>Five years' acute hospital experience required with preferred experience in critical care areas: Required</li><li>Two years' utilization review experience using the Optum/Inter Qual product within the last 12 months: Required</li></ul>Licenses/Certifications:<ul><li>Registered Nurse (RN) licensure in the state of practice: Required</li></ul>Essential Functions:<ul><li>Completes clinical reviews of acute medical patients using the Optum/Inter Qual tool to determine if the patient is in the right acute setting, receiving the right acute services, during the appropriate length of stay.</li><li>Participates in annual Optum/Inter Qual training required. Takes the required annual Optum/Inter Qual Interrater Reliability (IRR) test with a minimum passing score as defined in the yearly departmental goals.</li><li>Meets weekly productivity metrics within 90 days of completing orientation and maintains on a weekly basis as defined in the yearly departmental goals. Meets quality audit metrics within 90 days of completing orientation and maintained on the audit cadence set within the department as defined in the yearly departmental goals.</li><li>Completes all required departmental education assigned with timeliness and accuracy. Follows all departmental workflows in communication variances to the on-site care management teams when appropriate. Reviews and analyzes medical records to assess the necessity and appropriateness of treatments and interventions.</li><li>Collaborates with healthcare professionals to develop and implement comprehensive patient care plans. Facilitates communication between the patient, healthcare team, insurance providers, and other stakeholders to ensure a coordinated and efficient care process. Stays up to date with the latest healthcare regulations, insurance guidelines, and evidence-based practices to ensure the delivery of optimal healthcare services.</li><li>Performs other job-related duties as assigned.</li></ul>Organizational Requirements:Adventist Health is committed to the safety and wellbeing of our associates and patients. Therefore, we require that all associates receive all required vaccinations as a condition of employment and annually thereafter, where applicable. Medical and religious exemptions may apply.Adventist Health participates in E-Verify. Visit <a href="https://adventisthealth.org/careers/everify/" rel="nofollow">https://adventisthealth.org/careers/everify/</a> for more information about E-Verify. By choosing to apply, you acknowledge that you have accessed and read the E-Verify Participation and Right to Work notices and understand the contents therein.

RN, Care Manager, Utilization Management (Part-Time, Weekend)

Analysis Skills

Audit Metrics

Cadence

Clinical Validation

Communication Skills

Health Insurance

Health Plan

Healthcare

Insurance Regulations

Internal Rate of Return (IRR)

Medical Records

Metrics

Nursing

Patient Assessment

Patient Care

Patient Care Denials

Quality Metrics

Registered Nurse (RN)

Resource Management

Service Delivery

Stewardship

Utilization Management

Experienced RequiredBachelor's degree in a relevant scientific discipline (biology, biochemistry, immunology, etc.) with 3+ years of experience in quality control testing, analytical development, or GMP; OR a Master's degree in relevant scientific disciplines with 1+ years of experience . Work ConditionsMany roles must be able to work at either Orca Bio Sacramento location (3400 Business Dr. or 7910 Metro Air Pkwy) based on operational needs, as well as regularly participate in video-based meetings.

YEAR

More than one million people in the United States today are fighting blood cancer. While a traditional allogeneic stem cell transplant has been the best hope for many, the transplant itself can prove fatal or lead to serious conditions, such as graft vs. host disease. Orca Bio is a late-stage biotechnology company redefining the transplant process by developing next-generation cell therapies with the goal of providing significantly better survival rates with dramatically fewer risks.With our purified, high-precision investigational cell therapies we hope to not only replace patients' bloodand immune systems with healthy ones, but also restore their lives. We have built a state-of-the-art, 100,000-square-foot manufacturing facility in Sacramento, CA (7910 Metro Air Pkwy) to ensure the consistent and reliable delivery of our high-precision cell therapy products. This site is essential to advancing our clinical pipeline and supporting future commercial availability of our life-saving therapies. The Specialist, Quality Assurance position is a key role in meeting the quality policy through their management of the different quality systems, including production records and deviation system management. The ideal candidate will be responsible for managing the quality systems, including deviations, change control, corrective and preventive actions (CAPA), and document management. Additionally, this role involves making timely batch disposition decisions to ensure quality standards are met before product release, supporting the rapid processing times required by our product. You will have the unique opportunity to make a difference in the lives of many patients as Orca Bio develops next-generation cell therapies. Physical Demands <ul><li>Production Associate Roles: Must have visual acuity of 20/20 (corrected or uncorrected) and normal color vision to safely perform critical tasks such as visual inspection of materials, equipment, and labeling, including distinguishing color-coded components in a GMP environment. </li><li>Most roles must be able to meet cleanroom gowning requirements, including wearing full gowning (face coverings, gloves, hoods, goggles) for extended periods, as needed. Use of cosmetics (makeup, painted nails), jewelry, or facial piercings is not permitted in the cleanroom, and any skin conditions that cause shedding must be disclosed. </li></ul>Work Conditions<ul><li>Many roles must be able to work at either Orca Bio Sacramento location (3400 Business Dr. or 7910 Metro Air Pkwy) based on operational needs, as well as regularly participate in video-based meetings. Also, may be required to work scheduled overtime, weekends, or holidays based on business needs. </li></ul>Responsibilities Quality System Management: <ul><li>Oversee the management of quality systems including deviations, change controls, CAPAs, and document control. </li><li>Ensure that all deviations are investigated thoroughly and timely, identifying root causes and implementing effective corrective actions. </li><li>Review and approve change controls to ensure compliance with regulatory requirements and internal procedures. </li><li>Maintain and improve CAPA processes to ensure effective resolution of quality issues. </li></ul>Batch Disposition: <ul><li>Evaluate batch records and associated documentation to make informed batch release decisions. </li><li>Collaborate with manufacturing and quality control teams to ensure all products meet regulatory and quality standards before release. </li><li>Monitor and document any quality issues related to batch production and implement corrective measures as necessary. </li></ul>Document Management: <ul><li>Maintain the document management system to ensure all quality-related documents are accurate, current, and compliant with regulatory standards. </li><li>Conduct regular reviews of quality documentation to ensure adherence to established protocols and procedures. </li></ul>Regulatory Compliance: <ul><li>Stay informed of current regulations, industry trends, and best practices in pharmaceutical quality assurance. </li><li>Assist in preparing for internal and external audits, ensuring that all quality systems and documentation are audit-ready. </li></ul>Training and Support: <ul><li>Provide training and guidance to staff on quality systems, processes, and compliance requirements. </li><li>Serve as a point of contact for quality-related inquiries and issues, fostering a culture of quality within the organization. </li></ul>Continuous Improvement: <ul><li>Participate in continuous improvement initiatives to enhance the effectiveness and efficiency of quality systems and processes. </li><li>Identify areas for improvement within quality operations and suggest appropriate solutions. </li><li>Track completion of quality records and maintain metrics. </li><li>Perform other duties as requested by supervisor/manager to support Quality </li><li>Work collaboratively with cross-functional teams, including manufacturing, research and development, and quality assurance, to support the overall quality of cell therapy products. </li></ul>General Requirements<ul><li>Communicate effectively with team members and contribute to a positive and collaborative work environment </li><li>Actively participate in group and project teamwork; project and process improvements </li><li>Strong organizational skills and the ability to manage multiple tasks concurrently </li><li>Willingness to learn and adapt in a fast-paced, dynamic environment </li><li>Adhere to cGMP policies and procedures, including documentation activities </li><li>Able to wear appropriate personal protective equipment </li><li>Willingness to work overtime as required </li></ul>Experienced Required<ul><li>Bachelor's degree in a relevant scientific discipline (biology, biochemistry, immunology, etc.) with 3+ years of experience in quality control testing, analytical development, or GMP; OR a Master's degree in relevant scientific disciplines with 1+ years of experience </li><li>Understanding of FDA regulations, GMP compliance, and quality system processes </li><li>Experience in quality control or GMP within a cell therapy or biopharmaceutical manufacturing environment is preferred </li><li>Able to meet project and testing timelines </li><li>Detail-oriented with a commitment to data integrity and accuracy, and an ability to identify problems with data management </li><li>Able to work collaboratively to respond to changing priorities and challenges </li><li>Ability to work both independently and collaboratively with a multi-disciplinary team in a fast-paced and regulated environment </li><li>Prior experience doing internal audits and document control management </li></ul> $75,000 - $90,000 a year The anticipated annual salary range for this job is based on prior experience in the role/industry, education, location, internal equity, and other job-related factors as permitted by law. For remote-based positions, this range may vary based on your local market. Full-time employment positions will also be eligible to receive pre-IPO equity and annual bonus, in addition to competitive medical, dental, and vision benefits, PTO, 401(k) plan, life and accidental death and disability coverage, and parental leave benefits. Other perks include subsidized daily lunches and snacks at our on-site locations. Who we are We are driven by a passion for science and compassion for patients. We act with urgency to ensure our treatments are one day accessible to all who need them. We live by our core values of passion, courage, and integrity. Excellence in our work means the chance to unlock a better quality of life for our patients, and with that comes tremendous responsibility. We innovate on a path that hasn't been paved. We embrace an entrepreneurial spirit and take calculated risks to achieve our mission. We aren't afraid to ask "why not" and challenge the status quo. We maintain a start-up culture of camaraderie and leadership by example, regardless of title. We're proud to be an equal opportunity employer, and recognize that celebrating our differences creates stronger, lasting solutions that better serve our team, our patients and their healthcare providers. Notice to staffing firms Orca Bio does not accept resumes from staffing agencies with which we do not have a written agreement and specific engagement for a particular opening. Our employment activities, inquiries and offers are managed through our HR/Talent team, and all candidates are presented through this channel only. We do not accept unsolicited resumes, and we rarely outsource recruitment. We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

Weekend Healthcare Jobs in Auburn, CA

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Weekend Healthcare Jobs in Auburn, CA

Radiologic Technologist - Full Time - Weekends Only - Day Shift Mid-Columbia Medical Center

RN, Care Manager, Utilization Management (Part-Time, Weekend) Mid-Columbia Medical Center

Specialist, Quality Assurance - Weekend Shift (Friday-Monday) Orca Bio

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