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We are seeking a regulatory affairs specialist to assist with ensuring regulatory compliance. The Regulatory Affairs team is highly cross-functional and work will center on collaborating with internal scientific, business and operational teams to address compliance needs of our novel probiotics and dietary supplements.
ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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As part of the Regulatory Affairs Asia Pacific (APAC) team, on-site at our Diabetes Care Division HQ location in Alameda, CA. As an individual contributor, the function of a Regulatory Affairs Specialist is to provide support for the regulatory department to ensure efficient and compliant business processes and environment.
$65,900 - $131,900 a yearFull-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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As an individual contributor, the function of a Senior Regulatory Affairs Specialist is to provide support for the regulatory department to ensure efficient and compliant business processes and environment.
$83,600 a yearExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Regulatory Affairs Specialist II On-site in Alameda, CA. Provide consultation/advice to regulatory specialist for change control and product development. Handle regulatory activities involved in documentation, labeling, and field support.
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Medical Device regulatory affairs experience. 5+ years of regulatory affairs experience. Responsible for regulatory activities, including product registrations, impact assessment, etc.
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Experience working collaboratively across various departments, including Software Development, Clinical, Project/Product Management, Marketing, Regulatory Affairs, Labeling, and Legal. The Intermediate Quality Specialist will maintain a document revision control and numbering system, perform internal audits of all policies, procedures, work instructions and forms and maintain the Quality Manual with associated SOPs as defined by our corporate strategy.
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Exempt/Non Exempt: Non Exempt Years Experience: 2-5 years regulatory experience and/or 2 years relevant industrial experience typically with a quality, product-development/support, or scientific affairs function Skills: Knowledge of regulations and standards affecting IVDs and/or biologics Education: BS preferred in a technical discipline like biology, chemistry, microbiology, immunology, medical technology, etc.
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Exempt/Non Exempt: Non Exempt Experience: 2-5 years regulatory experience and/or 2 years relevant industrial experience typically with a quality, product-development/support, or scientific affairs function, 5 Required education level/certifications: BS, MS Skills: Knowledge of regulations and standards affecting IVDs and/or biologics Education: BS preferred in a technical discipline like biology, chemistry, microbiology, immunology, medical technology, etc.
ExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Under the direction of the Manager, Regulatory Affairs & Compliance, the Regulatory Compliance Specialist supports the compliance program by coordinating implementation of new and revised healthcare rules and requirements as are communicated by state agencies.
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Immediate hiring for Regulatory Specialist II. Provides consultation/advice to regulatory specialist for change control and product development. Regulatory Specialist II - Medical - W2 only.
ExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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This Senior Regulatory Affairs Specialist will have an opportunity to work on new to market technology that is improving the field of diagnostic imaging and saving patient lives. Senior Regulatory Affairs Specialist-Remote Based-West Coast.
RemoteExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Experience Background (Any): Medical Device, Pharmaceutical, Regulatory Affairs, Quality Assurance, SW Engineering, APAC regulatory submission, or APAC-related work under Quality Assurance/Engineering.
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Job Summary: Under the direction of the Manager, Regulatory Affairs & Compliance, the Regulatory Compliance Specialist supports the compliance program by coordinating implementation of new and revised healthcare rules and requirements as are communicated by state agencies.
Full-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Responsible for filing necessary applications and handling all government interactions pertaining to the regulation process for products requiring governmental approval.
ExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Collaborate with clinical development, regulatory affairs, biometrics, and related cross-functional teams to gather and integrate data into regulatory documents. Develop and implement a strategic plan for the company's medical writing activities, ensuring alignment with clinical development, regulatory affairs, and overall business goals.
Full-timeExpandApply NowActive JobUpdated 13 days ago
regulatory affairs specialist jobs in Oakland, CA
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