Collecting information
Organizing data
TravelNurseNetwork is working with Cynet Health to find a qualified Labor/Delivery RN in Redwood City, California, 94063!. Collaboration with the healthcare team is essential for ensuring optimal patient outcomes.. Applicants must be committed to continuous learning and professional development in maternal child health.. A focus on patient safety and high standards of care is paramount.. Matching talented nurses like you with high-paying travel jobs at the best facilities across all 50 states.
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.
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.
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.
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
Reproductive Partners San Diego is a leading Southern California fertility clinic, internationally and nationally recognized for our success in IVF - in vitro fertilization, egg freezing and other fertility treatments for our patients. The Medical Billing Specialist plays a key role in the financial operations of our fertility clinic by ensuring accurate and timely billing of patient accounts, insurance claims processing, and payment posting. Review and process daily billing for fertility-related services, including IVF, IUI, lab testing, and surgical procedures.. High school diploma or equivalent required; Associate’s degree or certificate in Medical Billing/Coding preferred.. Experience with medical billing software (e.g., eIVF, Nextech, Athena, or similar)
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.
We are 29,000 strong and operate 1,500+ pet care centers in the U.S., Mexico and Puerto Rico, including 250+ Vetco Total Care hospitals, hundreds of preventive care clinics and eight distribution centers.. Bachelor’s degree and 5+ years of experience in contract management, legal operations, or commercial negotiations.. Proficiency with contract management systems and Microsoft Office Suite; experience with tools like DocuSign, Salesforce, or CLM platforms is a plus.. Sr Supply Chain Manager / Senior Procurement Manager. Senior Employee Benefits Account Manager
Specific tasks may include design of clinical development program plans, as well as clinical protocol development, medical monitoring of clinical trials, and analysis of study data and preparation of trial reports and related regulatory documents.. This individual will have a solid understanding of all phases of clinical drug development with particular expertise in first in human/early phase clinical trials, translational science, and operational excellence.. Assist in the preparation and review of documents for regulatory reports including drafting of clinical scientific documents such as IND, IND amendments, Investigator Brochures, Annual Reports (DSUR), and other FDA/HA submissions. MD, DO, PharmD or equivalent degree with 5+ years of clinical/clinical research experience in academia, industry or similar setting with a minimum of 3 years of Biopharmaceutical Industry experience; 5+ years Biopharmaceutical Industry experience will be a plus. It is the policy of Qpex Biopharma to undertake affirmative action for protected veterans and individuals with disabilities in compliance with all federal, state, and local requirements to recruit a diverse pool of protected veteran and individuals with disabilities applicants and to ensure that our employment practices are, in fact, non-discriminatory.
Join to apply for the Quality Assurance Manager role at Cooper Steel. The Field Quality Manager is responsible for managing the implementation of quality procedures on construction project sites.. The Field Quality Manager coordinates with project managers, site supervisors, and quality inspectors to proactively address quality issues, reduce rework, and maintain documentation for compliance and reporting.. AWS Certified Welding Inspector (CWI). Sign in to set job alerts for “Quality Assurance Manager” roles.
This includes batch record review, review of raw materials, deviation investigation, label issuance, and word processing, tracking, issuing, distributing, and archiving company-wide GLP/GCP/GMP controlled documentation, training, and facility support systems. Support clinical product manufacturing by batch record review, label printing, product packaging, and shipping. Conduct or coordinate deviation investigations, corrective and preventative actions (CAPA), change controls, company-wide training, and internal audits. Process controlled documentation through the GxP (GLP / GCP / GMP) documentation system, including but not limited to word processing, tracking, issuing, distributing, and archiving, utilizing manual or an electronic document management system. Familiar with Quality Systems and records management in a cGMP environment.
It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organizations.. It also has a rapidly developing presence in highly specialized and molecular clinical diagnostic testing and in-vitro diagnostic products.. Knowledge of cGMP, GLP, Eudralex Volume 4, and ISO regulations are a plus.. Bachelor’s or Master’s degree in Chemistry or closely related science field from a four year college / university or equivalent education and job experience; at least one year of previous employment history in a regulatory environment such as GMP / GLP, ISO or equivalent.. Familiarity with at least one scientific technique (HPLC, GC, etc.)
The individual will be responsible for providing education and support to trial team staff in the implementation of, and adherence to processes and workflows, controlled documents, tools, and templates to enhance the quality of study documents and the TMF. Incumbent will identify process improvement opportunities and will support process re-engineering.. Incumbent will contribute to the development of training materials while serving as a subject matter expert in both QA, QC and TMF. Incumbent will participate in the creation of a quality and education program through which staff involved in the conduct of clinical research, therapeutic and non-therapeutic protocols, will be educated and trained on current industry standards.. Act as subject matter expert and TMF point of contact for study teams and partners. Performs key TMF duties in accordance with established guidelines and work instructions (e.g., TMF set-up, management, completeness and timeliness monitoring, reports and metrics, closeout, and TMF quality control (QC)/ quality assurance (QA) activities, etc.. Collaborate with study teams to ensure all appropriate documents have been filed prior to specific study milestones (e.g., site activation, amendments, close-out and TMF delivery) or according to contract requirements
Specialized experience must demonstrate the following: monitoring and evaluating contract quality assurance programs to ensure compliance with contract specifications for ship repair and overhaul.. Specialized experience must demonstrate the following: providing assistance in monitoring contract quality assurance programs to ensure compliance with contract specifications for ship repair or overhaul.. Successful completion of a master's degree or equivalent graduate degree with major study in quality assurance, statistics, mathematics, production management, industrial management, computer science, engineering, engineering technology, physical sciences, textiles, or another field related to the position.. A bachelor's degree with superior academic achievement with major study in quality assurance, statistics, mathematics, production management, industrial management, computer science, engineering, engineering technology, physical sciences, textiles, or another field related to the position.. Industries Government Administration and Strategic Management Services
It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organizations. It also has a rapidly developing presence in highly specialized and molecular clinical diagnostic testing and in-vitro diagnostic products. Knowledge of cGMP, GLP, Eudralex Volume 4, and ISO regulations are a plus. Bachelor’s or Master’s degree in Chemistry or closely related science field from a four year college/university or equivalent education and job experience; at least one year of previous employment history in a regulatory environment such as GMP/GLP, ISO or equivalent. Familiarity with at least one scientific technique (HPLC, GC, etc.)
Conducts surveillance of workforce activities and uses statistical sampling, audit, and observation techniques to evaluate compliance with policies and procedures and adherence to contract requirements.. Provides monitoring reports to QA Manager.. Computer literate, able to use various software programs for correspondence, reports, statistical compilation and analysis, and database access. With a dedicated and passionate team, Equus puts the industry’s best practices to work by focusing on the development, design, and delivery of demand-driven workforce solutions. Equus Workforce Solutions is proud to be an Equal Opportunity Employer.
The individual will be responsible for providing education and support to trial team staff in the implementation of, and adherence to processes and workflows, controlled documents, tools, and templates to enhance the quality of study documents and the TMF. Incumbent will identify process improvement opportunities and will support process re-engineering.. Incumbent will contribute to the development of training materials while serving as a subject matter expert in both QA, QC and TMF. Incumbent will participate in the creation of a quality and education program through which staff involved in the conduct of clinical research, therapeutic and non-therapeutic protocols, will be educated and trained on current industry standards.. Act as subject matter expert and TMF point of contact for study teams and partners. Performs key TMF duties in accordance with established guidelines and work instructions (e.g., TMF set-up, management, completeness and timeliness monitoring, reports and metrics, closeout, and TMF quality control (QC) / quality assurance (QA) activities, etc.). Collaborate with study teams to ensure all appropriate documents have been filed prior to specific study milestones (e.g., site activation, amendments, close-out and TMF delivery) or according to contract requirements