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Backgrounds preferred as Child Life Specialist (CLS), Certified Occupational Therapist Assistant (COTA), Speech Language Pathologist Assistant (SLPA), Developmental Interventionist (DI) or similar educational background.
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This includes, but is not limited to, Internal and External Audits, Regulatory Filing and Certifications, Regulatory Compliance activities, Change Control, Training, Document Control, Record Retention, Product and Customer Complaints Handling, and CAPA Program, which includes the Deviations, Corrective Action, and Preventive Action.
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Use sales planning and reporting system as directed.
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Ensure compliance with regulatory requirements for complaints by documenting them in GCMS Trackwise quality management system, and managing related follow up activities. Accountable for complying with all Regulatory requirements with respect to complaint handling and maintaining the accuracy of data within BSC business systems.
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Reporting to the School Director and under the direction of the Director of Student Support, the Education Specialist will work in close collaboration with the classroom Facilitator supporting all students in a general education classroom.
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A valid certificate from a Department of Consumer Affairs Medical Board-approved agency to work as a Medical Assistant:American Association of Medical Assistants. California Correctional Health Care Services (CCHCS) is dedicated to enhancing public safety and promoting successful community reintegration through education, treatment, and active participation in rehabilitative and restorative justice programs.
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Grounds Specialist (Full-Time) | SCI Jobs. Ability to operate hand-held tools and equipment, including, but not limited to a shovel, pick, rake, sledge hammer, lawn mower, weed trimmer and leaf blower.
$16.65 - $21.55 an hourFull-timeExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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As one of the most comprehensive social service agencies in LA County, MHALA provides integrated mental health, physical health, wellness, employment, housing, education and outreach services, with special programs for transition age youth and Veterans.
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Experience advising management officials on various HR processes and advising on the procedural and regulatory requirements governing HR functions and or processes and assisting and developing other HR personnel.
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Role Description We are Allianz Engineering, Construction & Power, one of the leading engineering insurance and inspection service providers in the UK. Our inspection service helps businesses evaluate their engineering risks and meet their health and safety, legislative and regulatory compliance requirements.
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Handle/manage all duties related to the execution of US/OUS Class 3 Medical Device Clinical Trials in line with GCP, Regulatory and Compliance requirements. This position plays a key role in the development and execution of pre-clinical, feasibility and first-in human trials intended to support regulatory registration of new indications and new medical devices, as well as physician-initiated and company sponsored, and grant funded clinical trials.
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Minimum of 12 months of Med/Surg/Telemetry or Critical Care nursing experience preferred with regard to regulatory guidelines and standard of practice and/or at the discretion of the Manager/ Director.
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Location: Remote (Virtual/Work From Home)
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Follow OSHA regulations and other regulatory agencies relating to job site safety, demonstrates safe work practices. ABOUT US Tremco Construction Products Group (CPG) brings together Tremco Incorporated's Commercial Sealants & Waterproofing and Roofing & Building Maintenance operating divisions; Dryvit Systems, Inc.; Nudura Inc.; Willseal; Weatherproofing Technologies, Inc. and Weatherproofing Technologies Canada, Inc. Structures with Tremco CPG systems are easier to build and maintain, virtually impervious to the elements, and can provide any look desired.
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Collaborate with other cross-functional teams (Quality, R&D, Regulatory, CROs, statisticians) Drive study related activities from pre-clinical/clinical protocol design to Human Factors input, data management, study start-up/execution/close-out for one or several studies.
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regulatory affairs jobs Title: regulatory affairs specialist Company: Amgen in Santa Clarita, CA
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