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Senior Regulatory Affairs Manager (EU) Procurement Operations Specialist (DCPROs), DCSP. Senior Product Manager - Technical , Customer Growth, Product Management, OTIE. Senior Regulatory Affairs Manager (EU.
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Similar Jobs (1) Sr. Specialist, International Regulatory Affairs, Critical Care locations USA - California – Irvine time type Full time posted on Posted 2 Days Ago. As a Senior Specialist, International Regulatory Affairs, you complete and maintain regulatory approvals and clearances of assigned products.
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We are looking for Senior Regulatory Affairs Specialist for our client in Irvine, CA. Job Title: Senior Regulatory Affairs Specialist. Participate in providing guidance and feedback to business unit regulatory teams on registration requirements for new and renewal registrations, product and process changes, and review of labeling content and guidance on process improvement projects, based on prior experience and responses from affiliates.
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Regulatory Affairs Specialist. Supports all business segment initiatives as identified by divisional management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements.
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Regulatory Affairs, Quality and Compliance, Product Management/Marketing. As we continue to grow as one, QuidelOrtho, we are seeking a Technical Communications Specialist II. The Technical Communications Specialist II produces technical publications and communications to support the safe and effective use and servicing of Ortho Products.
$53,000 - $96,000 a yearFull-timeExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Minimum of 3 years of labeling experience or relevant experience in the pharmaceutical industry (e.g., Medical Affairs, Regulatory Affairs, Clinical, Pharmacovigilance). The Global Labeling Therapeutic Area group is accountable for developing labeling content and maintaining the target product labeling for developmental products, Core Labeling documents (e.g., CCDS, CCPPI, CCIFU) and US labeling for marketed products; and supporting country Regulatory Affairs in the development and maintenance of the EU Labeling and other country's Local Labeling.
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Minimum 5 years in Regulatory Affairs, including leadership roles. Ensure effective execution for new innovative consumer-centric products and the life cycle management of products in the portfolio across the following regulatory classes (OTC monograph drugs, dietary supplements, cosmetics, foods and medical devices.
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Day-to-DayInsight Global is seeking a Regulatory Affairs Specialist to join one of our largest chemical and water clients in the Eagan area. This person will be working within the Regulatory Affairs division working with SDS' to ensure all proper information is relayed for products created by the organization and ensuring they are meeting federal, state, and national regulations.
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Pulmonx is looking for an experienced Sr Regulatory Affairs Specialist to join our dynamic Regulatory Affairs Team in Redwood City, CA! At least 5 years of regulatory affairs experience in the medical device industry or equivalent experience.
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Serving as regulatory labeling point of contact on global Regulatory Affairs sub-teams to ensure delivery of labeling documents that meet quality and compliance standards and regulatory labeling requirements to support timely regulatory submissions for assigned products.
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This role will interface with other Insulet departments (e.g. Research and Development, IT-Cybersecurity, Sustaining, Engineering, Human Factors, and Regulatory Affairs) as well as other external parties on issues related to product development, launched product support, and software used for automation of the quality system.
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Job DescriptionJob DescriptionSalary: Reporting directly to the Licensing and Regulatory Affairs Manager and indirectly to the Chief Executive Officer, the Environmental Health & Safety (EHS) Specialist will facilitate and maintain the Companys EHS programs and procedures and serve a subject matter expert for safety regulations and best practices.
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Full-time work experience related to pharmaceutical industry, supply chain management (distribution), regulatory affairs or equivalent education and experience. Conduct testing with vendors, customers and serialization providers to ensure successful connectivity.
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Interface with representatives from key functional groups (Monitoring, Data Management, Research & Development, Manufacturing, Sales, Marketing, Regulatory Affairs, Legal, and European Clinical groups.
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The main function of a regulatory affairs specialist is to complete and maintain regulatory approvals and clearances of assigned products. Title: Sr Regulatory Affairs Specialist.
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