A company is looking for a CMC Regulatory Affairs Specialist. ...
Regulatory Affairs Specialist (R&D/QA). Provide regulatory support for products that will be transitioning from the IVDD to IVDR CE Marking. Quality Assurance, Research & Development, Marketing) to collect and coordinate information and regulatory documentation to assemble IVDR compliant tec...
Key Responsibilities:Develop and implement the Quality Management System (QMS) and Technical Documentation for medical devicesCommunicate, manage, and train internal teams and external partners on regulatory and quality mattersMaintain and improve the QMS, integrate regulatory processes into busines...
Responsible for advancing regulatory labeling practices, enhancing labeling processes, and integrating technology to streamline future operations. Bachelor’s degree in Life Sciences, Regulatory Affairs, or a related field. Minimum of 7-10 years of experience in regulatory affairs or labeling f...
A company is looking for a Regulatory Affairs Senior Specialist in Sunnyvale, CA, US. ...
Regulatory Affairs Specialist (R&D/QA). Provide regulatory support for products that will be transitioning from the IVDD to IVDR CE Marking. Quality Assurance, Research & Development, Marketing) to collect and coordinate information and regulatory documentation to assemble IVDR compliant tec...
RRIC has enterprise-wide exposure to lines of business, regulatory and risk reporting stakeholders as well as the external financial reporting and regulatory reporting infrastructures and frequently coordinates with internal audit. Experience supporting Regulatory Exams (Domestic and Int'l), Audits,...
The Associate Director of Regulatory Operations - Labeling will lead and oversee the strategic and operational aspects of regulatory labeling for medical devices. Provide expertise in regulatory standards, mentor team members, and stay current with industry trends and regulatory changes. The positio...
Work with global regulatory affiliates to compile global regulatory impact for changes on commercialized medical device products. GCP (Good Clinical Practice), Regulatory Affairs Operations, Regulatory Affairs Strategy. Perform regulatory assessments for US, EU, and Canada for changes on commerciali...
RRIC has enterprise-wide exposure to lines of business, regulatory and risk reporting stakeholders as well as the external financial reporting and regulatory reporting infrastructures and frequently coordinates with internal audit. Experience supporting Regulatory Exams (Domestic and Int'l), Audits,...
Regulatory Affairs Specialist (R&D/QA). Provide regulatory support for products that will be transitioning from the IVDD to IVDR CE Marking. Quality Assurance, Research & Development, Marketing) to collect and coordinate information and regulatory documentation to assemble IVDR compliant technical f...
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A company is looking for a Senior Technical Program Manager. ...
A company is looking for a Project Manager, Deployment. ...
A company is looking for a Regulatory Affairs, Senior Associate. ...
A company is looking for a Director of Legislative & Regulatory Affairs. ...
A company is looking for a Senior Manager, Accounting Projects. ...
Key Responsibilities:Develop global regulatory strategies for Acute Care and Monitoring productsLead interactions with regulatory agencies and ensure compliance with regulationsProvide oversight of regulatory review of advertising and promotion materialsRequired Qualifications:Bachelor's Degree and ...
A company is looking for a Legal Quality Assurance Specialist for a remote IME position in the United States. ...
A company is looking for a Compliance Specialist. ...
A company is looking for a Project Manager. ...
A company is looking for a Regulatory Affairs Senior Manager - Regional Regulatory Lead. ...
A company is looking for a Quality Assurance Specialist. Key Responsibilities:Prepare and execute test plans for various types of testing during the CI/CD pipelineIdentify and track software defects, collaborating with development teams for resolutionDevelop and maintain test automation frameworks a...
A company is looking for a Director, Global Regulatory Affairs Lead Consultant. ...