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Minimum of 5 years of experience as a Developer/Business Systems Analyst with a focus on QMS in the medical device industry, including expertise in Post Market Surveillance, Complaints Management, CAPA, Nonconformance, and Regulatory Submissions.
$80 - $85 an hourExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Reporting to the Clinical Research Manager of Blood & Marrow Transplantation and Cell Therapy (BMT-CT), the Clinical Research Coordinator Associate will be conversant in the goals, mission and priorities of the Institute, and utilize this knowledge to to manage data, enroll and follow patients on trial, and assist with regulatory and financial requirements of the trials.
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This role is a unique opportunity for an experienced Clinical Operations Professional with technical expertise in managing Phase I-III clinical trials in an industry setting and who has a strong knowledge of clinical operations, Good Clinical Practice (GCP), and US Food and Drug Administration (FDA) regulatory requirements.
$75 - $90 an hourExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Partner with local management to develop and implement a site CAPA process to address EHS program deficiencies and ensure EHS regulatory compliance. Proven track record to quickly interpret complex regulatory issues and provide recommended course of action.
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Provide technical expertise for all EHS programs, biosafety, machine safety, industrial hygiene, laser safety, ergonomics, contractor safety, and emergency preparedness. Review, update, develop required EHS programs including, but not limited to: IIPP, HMBP, HAZCOM, EAP, SOPs, LOTO/HECP, Confined Space Programs, Fire Prevention Programs, Biosafety, Lab Safety, Hot Works Program, Radiation/Laser Safety, Warehouse Safety and Chemical Inventory.
$90,000 - $135,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Facilities and Data Center Technician III must possess an in depth level of knowledge and will be responsible for the operational integrity and regulatory compliance of the facilities and data center electrical, mechanical, fire life safety systems, and communications infrastructure.
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Role: OFSAA Technical LeadTechno Functional expertise on OFSAA FCCM suite of productsExperience in the data flow within OFSAA AML, KYC, ECMKnowledge on OFSAA CTR (Current Transaction Reporting) and CRR (Customer Regulatory Reporting)Experience in PL/SQLExperience in Oracle OJET, Oracle Forms Framework, HTML, CSS, JavaScript, and Shell script.
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Specific responsibilities include: - Champion security: Follow best practices to meet the high standard of regulatory data security requirements. Specific responsibilities include: - Champion security: Follow best practices to meet the high standard of regulatory data security requirements.
$144,000 - $240,000 a yearExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Consistently ranked as number one in the space, NICE Actimize experts apply innovative technology to protect institutions and safeguard consumers and investors assets by identifying financial crime, preventing fraud and providing regulatory compliance.
$150Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Support projects or other initiatives from cross-functional groups and departments (i.e., Project Management teams, Scientific group, Quality/Compliance, Data Management, Biostatistics and Regulatory Affairs), and ensure adequate safety support and timely update of safety information to internal and external stakeholders.
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As a trusted community member, the CHW has a deep understanding of community needs and plays an integral & multifunctional role serving as a liaison between the community and the CRC. The CHW provides outreach in community settings, screenings for Medi-Cal eligibility, and schedules one-on-one appointments for enrollment application assistance in compliance with state and federal regulatory requirements, SCFHP policies and procedures, and business requirements.
$56,387 - $81,761 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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We research, develop, and commercialize innovative digital health products and solutions by bringing together the full capabilities of our team, including product strategy and management, clinical expertise, partnerships, UI/UX design, usability research, clinical research and validation, software development, AI / Gen AI, and regulatory submissions.
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This role reports to the Senior Manager of Quality and Regulatory Compliance within the IC/SP business unit. Respond to internal and external customer and/or regulatory compliance requests.
$112,500 - $168,750 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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This high visibility position is pivotal to our success as an organization, as this person will be a conduit of information between key Cepheid stakeholders, external government and regulatory agencies, the medical profession, other healthcare providers, and scientific communities.
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Responsible for annual compliance documents, tests and required regulatory filings (Section 125 testing, 5500 filings, ACA Filing, SAR, EDD and VDI, PCORI, ADP/ACP testing, etc. The ideal candidate is a subject matter expert in benefits administration for health and welfare plans, retirement programs, leave of absence management, wellbeing programs, employee communication, governance, and compliance.
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regulatory job Title: regulatory affairs specialist Company: Parexel in Santa Clara, CA
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