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This Regulatory Affairs Manager – Digital Health Technology will work on-site at our Alameda, CA location in the Diabetes Care Division. This Regulatory Affairs Manager – Digital Health Technology will provide support for the regulatory department to ensure efficient and compliant business processes and environment.
$218,500 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Provide Materials Science support to global Product Stewardship initiatives and regulatory compliance as needed. Experience of Product Stewardship, Regulatory, Operational and/or Research & Development is preferred.
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Advance staff's existing expertise in defined areas of import/export compliance as needed by the business structure or the ongoing changes in the regulatory environment. Provide leadership and direction to ensure site compliance with all relevant US Customs regulations and trade laws, including 19CFR, 15CFR, FDA, USDA, and other US regulatory agency requirements.
$190,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Experience in one or more of the following areas: order management, order fulfillment, logistics, customer service, master scheduling, inventory planning, inventory control, manufacturing, supplier quality, regulatory affairs or engineering.
$190,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Knowledge of regulatory requirements and standards governing wastewater treatment, discharge, and environmental protection (e.g., EPA regulations, NPDES permits) Stay informed about emerging trends, technologies, and regulatory developments in wastewater treatment and process engineering, and apply this knowledge to project design and execution.
$145,300 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Cross-functional collaboration/interaction with Clinical Affairs, R&D, Regulatory, Quality, OEC, Legal, Global Marketing & Commercial teams. Creation of up-to-date clinical/medical content required for internal or external education surrounding products in the portfolio or disease state awareness, as well as review/approval of ad promo materials or other assets which require medical/legal/regulatory review.
$286,700 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Support all Company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements. Complies with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments.
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Business processes related Quality, Regulatory, Environmental Health & Safety and Building security systems. Responsible for delivery of projects with multiple systems within the Quality, Regulatory and Engineering domains.
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Our Plano or Austin, Texas locations, currently have an opportunity for a Regulatory Affairs Manager. Experience acting as liaison between the Company and the various appropriate regulatory agencies, ensuring that communications on both sides are germane, specific and convey all necessary detail.
$190,000 a yearFull-timeExpandApply NowActive JobUpdated 23 days ago - UpvoteDownvoteShare Job
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Understanding of FDA regulatory issues related to medical device products and/or diabetic disease states is helpful but not required. Project coordination with internal cross-functional teams consisting of R&D, Regulatory, Legal, Purchasing, Operations, and Quality to develop packaging and labeling items for new products or revisions to existing products.
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Contributes to the development, establishment and maintenance of supplier quality engineering methodologies, systems and practices which meet company and regulatory requirements. Abbott Rapid Diagnostics is part of Abbott’s Diagnostics family of businesses, bringing together exceptional teams of experts and industry leading technologies to support diagnostic testing which provides important information for treatment and management of diseases and other conditions.
$145,300 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Abbott is a global healthcare leader that helps people live more fully at all stages of life. Abbott is an Equal Opportunity Employer, committed to employee diversity. At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life.
$39.15 an hourFull-timeExpandApply NowActive JobUpdated 22 days ago - UpvoteDownvoteShare Job
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Interacts directly with functional groups including R&D groups, Preclinical, Regulatory, Analytical Chemistry, and Quality groups in the Abbott various business Divisions and CROs. Senior-level contributor responsible for serving as a lead SME in biocompatibility and focuses on the toxicological and biocompatibility evaluation of products and technologies required for product approvals and patient safety of Abbott medical devices in accordance with applicable global regulatory guidelines.
ExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Coordinate and lead regulatory compliance activities related to the EHS programs and Abbott GEHS Technical Standards. Review new hazardous materials and assess incoming material for Safety Data Sheets (SDS), unique usage, storage characteristics, regulatory requirements, and exposure controls.
$96,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Working at Abbott. Experience with laser cutting, electro polishing, coil winding and braiding preferred.
$46.45 an hourFull-timeExpandApply NowActive JobUpdated 1 month ago
regulatory job Company: Abbott in Beech-grove, Indiana
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