Collecting information
Organizing data
Hours: Monday - Friday 8 AM - 5 PM Potential Saturdays.. Additional Info: The Lead Clinician provides direct behavioral health services and ensures clinical procedures are followed across the organization. This role supervises designated Behavioral Health Clinicians (BHCs), provides consultation on complex cases, participates in chart reviews and case conferences, and collaborates with interdisciplinary teams to improve patient care and clinic operations. The clinician delivers routine, acute, and preventive behavioral healthcare, assesses and treats a range of conditions, and ensures accurate, timely documentation in the EHR. The position supports quality improvement initiatives and fosters a patient-centered environment. Requires a Ph. D./Psy. D., MSW, or MFT degree; CA licensure as a Psychologist, LCSW, or LMFT; 3+ years of clinical experience; and strong knowledge of trauma-informed care, crisis intervention, and EHR systems.
Our mission is to help people lead healthier, more fulfilling lives by improving access to trusted, affordable, and personalized mental healthcare. We are actively looking to hire talented Psychiatric Nurse Practitioner in the San Marcos area, who are passionate about patient care and committed to clinical excellence. Telemedicine and in-person flexibility. LifeStance is a national provider of mental healthcare services focused on evidenced-based, medically driven treatment services for children, adolescents and adults suffering from a variety of mental health issues in an outpatient care setting, both in-person at its clinics nationwide and through its digital health telemedicine offering. The company employs psychiatrists, psychologists, psychiatric nurse practitioners, and licensed therapists throughout the US.
We are only considering candidates local to the Northfield, IL location at this time.. JOB SUMMARY: Audit a broad, global supplier base against FDA regulations, ISO standards, and other applicable global regulatory requirements across the full spectrum of Medline products including sterile products, APIs, raw materials, medical devices, pharmaceuticals, biologics, cosmetics, medical foods, and dietary supplements, as well as contract sterilizers and laboratories.. Perform internal audits of Medline divisions and manufacturing sites.. Lead complex, critical, supplier regulatory projects involving cross-functional teams.
Director of Patient Care Services (DPCS)- Home Health - Registered Nurse (RN). We are seeking an experienced Director of Patient Care Services or RN Clinical Supervisor for San Diego, CA. RN License Required.. This is a full-time, permanent, salaried position with a trusted Home Health and Hospice operator.. Experience working in long-term care, hospice, home health, palliative care, or hospital environment — preferably as a Nursing Director or DON. Has been featured in The Wall Street Journal, Fortune, Business Week, CNN
We are only considering candidates local to the Northfield, IL location at this time.. JOB SUMMARY: Audit a broad, global supplier base against FDA regulations, ISO standards, and other applicable global regulatory requirements across the full spectrum of Medline products including sterile products, APIs, raw materials, medical devices, pharmaceuticals, biologics, cosmetics, medical foods, and dietary supplements, as well as contract sterilizers and laboratories.. Perform internal audits of Medline divisions and manufacturing sites.. Lead complex, critical, supplier regulatory projects involving cross-functional teams.
Medical Devices Systems Engineer.. opportunity with long-term potential and is located in.. San Diego, CA (Hybrid). Please review the job description below and contact me ASAP if you are interested. Employee benefits include, but are not limited to, health insurance (medical, dental, vision), 401(k) plan, and paid sick leave (depending on work location).
Perform selected nursing and administrative/clerical duties that assist in the delivery of primary health care and patient care management under the direction of a physician.. · Under proper supervision by a physician and/or laboratory director, perform specimen collection and simple laboratory testing common to a private medical practice, such as: urine drug tests, breath alcohol tests, urinalysis, blood glucose by finger sticks, etc.. · Prepare and maintain supplies and equipment for treatments, including sterilization.. · Adjust to quality assurance policies and procedures concerning all physical therapy issues.. · Obtains revenue by recording and updating financial information; recording and collecting patient charges; controlling credit extended to patients; filing, collecting, and expediting third-party claims.
Summary: Directly reports to QA & EHS Director.. Bachelor's Degree/Trade School/Military Service may be substituted with GED minimal education and specialized training and certifications in Quality Assurance with 5 years total waterfront experience with 3 years Quality Assurance experience to include NAVSEA Standard Item Compliance experience.. Safety, Quality Assurance and NAVSEA Standards for shipboard work.. Knowledgeable in shipyard, maritime, and commercial work practices, quality assurance, safety, Metal-work and contracting methods.. Knowledge of OSHA Regulations for Shipyard Employment, NAVSEA Standard Items, Joint Fleet Maintenance Manual (JFMM), NAVSHIPS Tech Manuals (NSTM), Level I, and DOD Standards, Military Specifications, Performance Standards, and other customer related specifications and standards.
Mirador is a next-generation precision medicine company focused on immunology and inflammation.. We are seeking a motivated individual to join our Regulatory Affairs team and be responsible for leading development and implementation of regulatory CMC strategy primarily for biological assets.. Plan, prepare, author, and / or review CMC-focused content for health authority submissions (e.g., scientific advice briefing packages, CTA, MAA) to health authorities to support clinical trials, registration, maintenance of registration, post-approval registration changes, and / or labeling of pharmaceutical products.. Drive strategy for M3 content for IND / IMPD / CTA and NDA / BLA / MAA in collaboration with CMC and Quality colleagues.. Global Regulatory Affairs CMC experience with biologics.
Fate Therapeutics is looking for an Executive Director or Senior Director in Regulatory Affairs to oversee and direct the strategic planning and execution of clinical regulatory activities essential for initiating and conducting clinical trials and securing regulatory approvals.. Provide strong cross-functional leadership for global filings including authoring/reviewing sections of IND/CTA, NDA/BLA/MAA, and other global submission documents in support of clinical trials and marketing applications, as well as their amendments, in conformance with local regulatory requirements.. Qualifications BS/MS/PhD degree in a life science with at least 12 years of progressive experience in Regulatory Affairs in the biotechnology or pharmaceutical industry.. Previous cell therapy product experience and regulatory knowledge is highly preferred.. Fate Therapeutics is a clinical-stage biopharmaceutical company dedicated to bringing a first-in-class pipeline of induced pluripotent stem cell (iPSC)-derived cellular immunotherapies to patients with cancer and autoimmune diseases.
What are we looking for in our Quality Assurance Analyst 2?. The Science Team at Russell Tobin & Associates is supporting a Medical Device organization that has an opening for Quality Assurance Analyst near San Diego, CA !. Join the QA Compliance team at Dexcom to support key quality functions including CAPA, Non-Conforming Events (NCE), Nonconforming Material Reports (NCMR), and Internal Audits. Experience with QMS in a regulated industry (medical device preferred).. We are the staffing arm of the Pride Global network, a minority-owned integrated human capital solutions firm, with additional offerings in vendor management, payroll programs, and business process optimization.
This position will serve as a construction quality assurance (QA) representative responsible for assisting Customs and Border Protection (CBP) in execution of construction along the borders of the United States.. This is a full-time, temporary position lasting 12-36 months.. Proficiency with project management software (Procore, Autodesk, etc. Ability to pass a government background investigation, including financial, criminal, residential, educational, foreign affiliation, prohibited substance use, and employment verifications; active U.S. Customs and Border Protection background investigation preferred.. Create a job alert for this search Quality Assurance Analyst
Alchemy Global Talent Solutions is supporting a global leader in the medical device manufacturing industry in the search for a Manufacturing Engineer to join their high-performance engineering team at a high-volume, fully automated facility in South Carolina.. Operating within an FDregulated, GMP-compliant environment, the role plays a critical part in improving equipment performance, reducing waste, and delivering process excellence.. Provide hands-on support in the troubleshooting and optimisation of cam-driven, pneumatic, and hydraulic production systems.. Demonstrated ability to lead process improvement initiatives using Lean Manufacturing methodologies.. Six Sigma certification (Green Belt or Black Belt) preferred.
Overview This position will serve as a construction quality assurance (QA) representative responsible for assisting Customs and Border Protection (CBP) in execution of construction along the borders of the United States.. This is a full-time, temporary position lasting 12-36 months.. Monitor the layout of work and inspection of all work in progress.. Proficiency with project management software (Procore, Autodesk, etc. Ability to pass a government background investigation, including financial, criminal, residential, educational, foreign affiliation, prohibited substance use, and employment verifications; active U.S. Customs and Border Protection background investigation preferred.
This is a float pool position that services the following Sharp Rees-Stealy locations: Rancho Bernando, San Diego Main, Scripps Ranch, and Sorrento Mesa.. California Licensed Vocational Nurse (LVN) - CA Board of Vocational Nursing & Psychiatric Technicians -REQUIRED. Patient/Guardian Education - Provide education as appropriate for: child development, asthma, autism, breastfeeding, healthy eating, use of medication equipment and/or medical equipment (i.e. Albueterol inhaler, crutches, etc. Skills as a Licensed Practical Nurse or Licensed Vocational Nurse.. Pediatric Advanced Life Support (PALS) - American Heart Association; California Licensed Vocational Nurse (LVN) - CA Board of Vocational Nursing & Psychiatric Technicians; AHA Basic Life Support for Healthcare Professional (AHA BLS Healthcare) - American Heart Association; Other
This role will be responsible for effectively facilitating change in care delivery by implementing best practices and procedures that positively impact the health care ecosystem as it relates to brain health initiatives (mental/behavioral health, dementia). The Senior Manager, Health Care Transformation will be responsible for creating, leading, and implementing changes to practice, process, and policy, as well as facilitating strategic conversations with the aim of developing national brain health programs. This role will collaborate closely with the Senior Director, Clinical Research & Telehealth to ensure the success of all initiatives. Convene strategic partners to generate new ideas and program opportunities related to brain health, including funders, policy makers, and key stakeholders.. Graduate degree in healthcare administration, public health, organizational leadership, or other related discipline
From our world-renowned Radiation Oncologists, highly trained Registered Nurses, Medical Physicists, Dosimetrists, and Radiation Therapists, and everyone in-between, our team of professionals works collaboratively to bring hope and healing to even the most aggressive cancer cases.. The Clinical Coordinator helps support and coordinate patient access, appointments and medical information and is the primary clinical contact which functions as a Navigator and Patient Advocate between patient, their family and the care team.. Serve as resource for information about services provided for inquiries from physician offices, potential patients and families from outside San Diego County.. Demonstrate proficiency of computer applications and EHR systems. Current Licensed Vocational Nurse (LVN) Certification
The role requires a deep understanding of clinical trial processes, regulatory compliance (GCP, FDA, ICH), and the ability to lead cross-functional teams to ensure high-quality, timely, and cost-effective trial execution.. Ensure inspection readiness at all times, including regular review of the Trial Master File (TMF).. Work closely with internal stakeholders including Clinical Development, Regulatory Affairs, Medical Affairs, and CMC to ensure alignment and smooth execution of clinical programs.. Proven track record of leading trials from start-up through close-out, including protocol development, site initiation, vendor management, and data review.. Strong knowledge of ICH GCP, FDA regulations, and global clinical research guidelines.
Employment Type: Contract on W2 (US Citizens or GC Holders Only). Job Description The Specialist, Clinical Customer Advocacy, is responsible for complaint management and event reporting, ensuring regulatory compliance with medical device reporting standards for domestic and international agencies.. Ensure timeliness and compliance with FDA regulations related to complaint review.. Coordinate and prepare responses for FDA and global regulatory agencies.. Education and Experience Bachelor’s degree in chemistry, engineering, nursing, or related fields preferred.
This position will serve as a construction quality assurance (QA) representative responsible for assisting Customs and Border Protection (CBP) in execution of construction along the borders of the United States.. This is a full-time, temporary position lasting 12-36 months.. Proficiency with project management software (Procore, Autodesk, etc. Ability to pass a government background investigation, including financial, criminal, residential, educational, foreign affiliation, prohibited substance use, and employment verifications; active U.S. Customs and Border Protection background investigation preferred.. Create a job alert for this search Quality Assurance Analyst