Director Of Outpatient Quality, Network Administration, Full-Time, Days MarinHealth Medical CenterDirector Of Outpatient Quality, Network Administration, Full-Time, DaysNovato, CaliforniaMarinHealth is already realizing the benefits of impressive growth and has consistently earned high praise and accolades, including being Named One of the Top 250 Hospitals Nationwide by Healthgrades, receiving a 5-star Ranking for Overall Hospital Quality from the Centers for Medicare and Medicaid Services, and being named the Best Hospital in San Francisco/Marin by Bay Area Parent, among others. Reporting to the VPMA and Executive Director of Quality, the Director of Outpatient Quality is responsible for clinical quality strategy development, clinical data analytics, regulatory readiness, supporting a thriving patient safety/risk safety culture through cross-functional collaboration to ensure the consistent delivery of high-quality, patient-centered care.
Compliance QA Director Exelixis IncCompliance QA DirectorAlameda, CA$190,000–$269,000 / yearli>Acts as the Subject Matter Expert for current global regulatory compliance expectations and proactively reviews changes in regulatory requirements and industry environment that would necessitate future changes and drives completion of impact assessments. Responsible for setting the strategic plan for maintaining organizational inspection readiness across the organization and developing an annual inspection readiness plan, ensures activities are completed, and drives continuous improvement initiatives.
Home Health Director of Quality Outcomes CompassusHome Health Director of Quality OutcomesPetaluma, CA$124,180–$153,632 / yearS/he audits documentation, compiles and reviews clinical performance data for quality and regulatory compliance, participates in activities to support survey readiness, provides education to support clinical development and positive outcomes, and works closely with Program leadership. Collaborates effectively with Home Health Regional Executive of Clinical Operations, Director(s) of Clinical Services and members of senior leadership to assure clinical excellence in each location.
Manager/ Director of Quality Assurance Crystal PharmatechManager/ Director of Quality AssurancePleasanton, CaliforniaOur guiding principle of "getting the crystal form and formulation right the first time for Phase I" not only expedites the progression of your molecule to IND filing and Phase I clinical trials, but also minimizes the necessity for human PK bridging studies. Our key differentiator is our integrated and specialized services, including API solid-state research, crystallization, preformulation, formulation development and manufacturing, clinical supply.
Manager/ Director of Quality Assurance CRYSTAL PHARMATECH INCManager/ Director of Quality AssurancePleasanton, CA10+ years of relevant regulatory affairs experience in the bioanalytical CRO or biotechnology/pharmaceutical industry, or a combination of education and experience. Crystal Bio Solutions, a member of Crystal Pharmatech, is a leading biologics analytical organization with operations in the San Francisco Bay Area and New Jersey.
Director of Quality Engineering Netskope IncDirector of Quality EngineeringSanta Clara, CAp>This is a high-impact technical leadership role perfect for a hands-on seasoned QE leader who has experience running large quality engineering and tool development organizations. Oversee the long term testing / pre-production environment strategy, ensuring high availability and stability for testing environments used by the entire company.
Senior Director of Quality Assurance Jones Lang LaSalle IncSenior Director of Quality AssuranceOakland, CA$192,000–$210,000 / yearData and Metrics Governance • Understand and support existing key performance indicators (KPIs) and quality metrics to ensure process improvements align with organizational objectives • Assess impact of proposed system and data changes on established governance frameworks and data integrity • Collaborate with data governance teams to evaluate risks and opportunities related to metrics and reporting when implementing process changes • Analyze performance data to identify trends, opportunities, and areas for improvement while maintaining alignment with existing measurement systems. • Model: Operational Excellence Focus • Location: San Francisco Bay Area preferred; other northern California locations considered • Success Metrics • Successful implementation of quality improvement initiatives • Measurable improvements in operational KPIs and process efficiency • Effective stakeholder engagement and cross-functional collaboration • Timely completion of assigned projects and deliverables • Knowledge transfer and capability building within client organization.
NewDirector of Quality Excellence PHILDirector of Quality ExcellenceSan Francisco, CaliforniaRemoteThrough its digital stakeholder experiences, patient access services, market access solutions, and distribution models, pharma manufacturers can deliver affordable and timely therapy access to patients, resulting in more patients staying on their treatment plans longer. Demonstrated ownership of software quality assurance for operational or customer-facing platforms, including test automation, release validation, and partnering with Engineering on defect prevention and resolution.
Director, Quality (Clinical) Braveheart BioDirector, Quality (Clinical)San Francisco, CaliforniaThe Director of Quality will serve as a senior quality leader for Braveheart Bio and will be responsible for clinical quality oversight, clinical data integrity, GCP inspection readiness, and support of nonclinical quality activities as needed for our late-stage clinical program in hypertrophic cardiomyopathy (HCM). This leader will partner closely with Clinical Development, Regulatory, Biometrics, PV, Data Management, Medical, Legal and external CRO and vendor partners to ensure effective, inspection-ready clinical quality oversight across all programs.
NewSenior Manager/Associate Director, Quality Countable LabsSenior Manager/Associate Director, QualityPalo Alto, CA$180,000–$215,000You will partner directly with R&D, engineering, manufacturing, and external partners (CDMOs and suppliers) to set quality strategy, drive execution, and establish the systems and culture needed for long-term regulatory readiness. Lead risk management activities (e.g., FMEA, risk assessments, hazard analysis) across product lines; ensure risk files are current, properly documented, and integrated into design and manufacturing decisions.
GCP/GVP QA Director Exelixis IncGCP/GVP QA DirectorAlameda, CA$185,000–$263,000 / yearp>The GCP/GVP QA Director is accountable for Good Clinical Practices (GCP) and Good Pharmacovigilance Practices (GVP) systems and activities, drives compliance and continuous improvement, ensures that Quality is integrated throughout GCP/GVP processes, supports internal/external audits, implements Quality Risk Management (QRM), tracks and trends key metrics, and ensures clinical data integrity. EDUCATION/EXPERIENCE/KNOWLEDGE & SKILLS: Education: BS/BA degree in related discipline and a minimum of 13 years of related experience; or, MS/MA degree in related discipline and a minimum of 11 years of related experience; or, PhD in related discipline and a minimum of 8 years of related experience; or, Equivalent combination of education and experience.
NewDirector of Quality Pivotal Systems Corp IncDirector of QualityFremont, CAReporting to the Chief Technology Officer (CTO), you will lead the Quality Engineering function and work closely with cross-functional teams to establish and maintain robust quality assurance processes throughout the product life cycle. Testing and Validation: Oversee the design and execution of testing processes, including automated and manual testing, to validate software functionality, performance, and security.
Director of Quality Assurance, Clinical Caribou Biosciences, Inc.Director of Quality Assurance, ClinicalBerkeley, CA$220,000–$235,000 / yearli>Provide Clinical Quality Assurance (GCP) strategic and technical leadership and Subject Matter Expertise (SME) to clinical study teams; Partner with the teams to effect appropriate and timely documentation of quality event management, including CAPA plans in support of product pipeline. The successful candidate must have the ability to execute QA tasks independently; effectively represent QA in a GCP, PV, and GLP focused team settings and manage quality related activities related to clinical vendors, investigator sites and regulatory agencies.
Director, Global Supplier Quality Management BioMarin Pharmaceutical IncDirector, Global Supplier Quality ManagementCA$176,000–$242,000 / yearn n nn nn nnn n n nt ttntt nttttttntttt ntttttSearch JobsntttttntttttLocationntttttntttttSearch RadiusnttttttttttnttttttWithin 25 milesnttttttWithin 50 milesnttttttWithin 100 milesnttttttWithin 250 milesnttttttWithin 500 milesnttttttWithin 1,000 milesnttttttWithin 2,000 milesnttttttWithin 5,000 milesntttttntttttntttttntttttntttt ttttntttntt ttnt n nnn nt nt ntt nttt ntttt Youxe2x80x99re leaving the BioMarin website. b'nnnnnnnn Director, Global Supplier Quality Management - BioMarin Corporatennnn n n nnntntntntntntntntntntntntntntntntnnnnnnnnnnnnnnnnnnnnnn nn n n n n tttt n n n n n n n Companyn n n About Us n Leadership Team n Board of Directors n Responsibility n Giving n Patient Support n n n n n n Sciencen n n Our Science n Research & Development n Manufacturing n Clinical Trials n Publications n External Scientific Support n n n n n n Products & Pipelinen n n Overview n Products n Pipeline n Expanded Access n Medical Information n n n n n n Newsn n n Newsroom n Stories n Press Releases n Company Statements n n n n n n Careersn n n Careers at BioMarin n Fellowships n n n n n n Investorsn n n n n n n Locations n Contact n n n ttttttn n n n n Locations n Contact n n n n n n n n Searchn n n n tn tttttttttttttttn n n n n n n n n n tttttttn n n n n n ttn n n n n Search BioMarinn n n n n n n n nnn n n n n Back to Jobsn n n nn nn n n nn n n n n n United Statesn n n n n n n BioMarin Pharmaceuticaln nn n n Director, Global Supplier Quality Management n Location: United States n Workstyle: Remote Only n Apply n nn n Who We Are n BioMarin is a leading, global rare disease biotechnology company focused on delivering medicines for people living with genetically defined conditions.
Medical Director, Utilization Management - Promise Blue Cross and Blue Shield AssociationMedical Director, Utilization Management - PromiseOakland, CAp>Finally, at the direction of the Promise Chief Medical Officer or VP, Medical Director, Medical Management, the Medical Director will be responsible for engaging in organization-wide quality improvement efforts and promoting a culture of continuous improvement throughout the organization and contracted provider partners in each regional market. The Medical Director serves as a role model for other clinical staff and is a knowledgeable resource in Medi-Cal regulatory requirements, measurement of health care quality (HEDIS and CAHPS) and California Department of Health Care Services' population health strategies to reduce health care inequities in vulnerable populations and communities.
Assistant Director UCSF Medical CenterAssistant DirectorSan Francisco, CAJob Summary: Under the supervision of the Associate Director for Clinical Research Programs, the Assistant Director, Clinical Research Operations, oversees the day-to-day staffing operations of their assigned research programs, including Clinical Research Managers, Clinical Research Supervisors and/or senior staff. The Assistant Director will manage 4 - 5 direct reports at the Clinical Research Manager (Clin Rsch Supv 2), and Clinical Research Supervisor (Clin Rsch Supv 1) levels, provide management oversight of approximately 20-25 FTE clinical research staff (Clinical Research Supervisors, Sr.
NewLead Quality Systems Engineer The Hiring MethodLead Quality Systems EngineerFremont, CaliforniaThis is a highly visible role responsible for leading the site's Quality Management System (QMS), ensuring ISO 9001 compliance, driving continuous improvement initiatives, and partnering across Engineering, Manufacturing, Operations, Corporate Quality, and executive leadership. Reporting directly to the Director of Quality & Reliability, this individual will become the site's primary quality systems expert, leading internal and external audits, managing quality documentation, improving Cost of Quality (COQ) metrics, and helping prepare the organization for continued growth.
Lab Assistant UCSF Medical CenterLab AssistantSan Francisco, CADuties include (but not limited to) checking, measuring, and cutting the small hair sample to the Sponsor's determined length and further cutting the samples into smaller pieces into a vial; weighing the appropriate amount of the cut hair per the requested method into a test tube in preparation for the drug analysis; calibrating the laboratory balances; helping to check, print, and file iMonnit and change the freezer and refrigerator charts; helping to log in hair samples received from clinical studies from the NIH-supported HIV clinical trials network (utilizing the laboratory information management system (LDMS) for specimen tracking and inventory storage); helping to organize inventory and stored hair samples; aiding in calibrating pipettes and fixing equipment; and other miscellaneous office and laboratory duties. The UCSF Hair Analytical Laboratory (HAL) - based in the Division of HIV, Infectious Diseases and Global Medicine - analyzes antiretroviral, anti-tuberculosis (anti-TB), antibiotic, and controlled substance concentrations in small hair samples (but may include other biological specimens such as plasma, serum, whole blood, dried blood spot (DBS), urine, nail, etc.) as biomarkers of adherence and exposure to anti-HIV and/or anti-TB therapy and in the context of HIV and TB prevention and treatment studies using assays developed and validated according to the Federal Drug Administration (FDA) guidance for bioanalytical methods and the National Institute of Health's (NIH's) Division of AIDS' (DAIDS) Clinical Pharmacology Quality Assurance Program (CPQA).
SUD California Based Group Facilitator Charlie HealthSUD California Based Group FacilitatorSan Francisco, CARemotep>By clicking "Submit application" below, you agree to Charlie Health's Privacy Policy and Terms of Service.. Participate in collaborative Therapy Treatment Team (Tuesdays) and Group Supervision (every other Friday) with your assigned Charlie Health Group Quality Supervisor or Group Quality Director, peers and other Clinical Leadership team members.
Senior Director / Director - CMC/GMP Quality Assurance Semnur, Inc.Senior Director / Director - CMC/GMP Quality AssurancePalo Alto, CA$235,000–$285,000p style="margin:0in 0in 8pt;line-height:107%;font-size:11pt;font-family:'calibri' , sans-serif;color:black">We are looking for an enthusiastic and talented Chemistry, Manufacturing, and controls (CMC) -Good Manufacturing Practice (GMP) Quality Assurance candidate (CMC-GMP QA) who is experienced in the current good manufacturing practices (cGMP) related quality assurance, and who thrive on challenges and changes of Chemistry, Manufacturing and Controls area, who can roll up their sleeves, put on multiple hats and have a can-do attitude without a lot of oversight or instruction. product development records, manufacturing batch records (MBR/EBR), process validation records (PV/PPQ), analytical records (AD/AV), release/disposition of GMP batches, product quality complaints.
RN Part Time PACS Group IncRN Part TimeCAli>Develop and maintain a good working rapport with inter-department personnel, as well as other departments within the facility to ensure that nursing services and activities can be adequately maintained to meet the needs of the residents. • Assist the Director and/or Infection Control Coordinator in identifying, evaluating, and classifying routine and jobrelated functions to ensure that tasks in which there is potential exposure to blood/body fluids are properly identified and recorded.
RN PRN PACS Group IncRN PRNCAli>Develop and maintain a good working rapport with inter-department personnel, as well as other departments within the facility to ensure that nursing services and activities can be adequately maintained to meet the needs of the residents. • Assist the Director and/or Infection Control Coordinator in identifying, evaluating, and classifying routine and jobrelated functions to ensure that tasks in which there is potential exposure to blood/body fluids are properly identified and recorded.
NewRN - Part-Time Weekend PACS Group IncRN - Part-Time WeekendCAli>Develop and maintain a good working rapport with inter-department personnel, as well as other departments within the facility to ensure that nursing services and activities can be adequately maintained to meet the needs of the residents. • Assist the Director and/or Infection Control Coordinator in identifying, evaluating, and classifying routine and jobrelated functions to ensure that tasks in which there is potential exposure to blood/body fluids are properly identified and recorded.
NewSCM Manager UCSF Medical CenterSCM ManagerSan Francisco, CAResponsible for managing and coaching a team of hospital laboratory technicians in a fast-paced environment; maintaining adequate staffing levels by scheduling coverage and evaluating workload for 24 hours/7-day operation; reviews and updates existing procedures and teaching materials to employees, CLS, and phlebotomy students; responsible for quality assurance and performance/process improvement in SCM. May also require knowledge of highly technical sub-specialty areas, such as, but not limited to, enzyme assay, steroid assay, radioimmunoassay, toxicology, electrophoresis, rheumatology, tissue typing, virology, sequencing, genomics, precision medicine, and other specialized send-out/reference lab/ specialty lab testing.