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Abbott is seeking a passionate, experienced Senior Regulatory Affairs Specialist to join our team on-site in Plymouth, or St. Paul, MN. In this role, you will lead the preparation and submission for regulatory approvals and identify and resolve problems.
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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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Collaborate cross-functionally with research, translational, clinical, and regulatory teams to advance cell therapy programs from preclinical development through to clinical trials and commercialization.
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Support Sr Stock Plan Administrator with maintenance of company’s equity data using Fidelity Stock Plan. Ensure global equity reporting and compliance with international tax and regulatory requirements, including year-end equity related tax filings.
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What you will Bring: Juris Doctorate degree from an accredited Law SchoolActive license to practice law, with either admission to the bar of the State of Minnesota or a limited in-house counsel license to practice law in the State of Minnesota 4+ years of in-house, law firm and/or regulatory agency experience in the areas of ethics and compliance.
$113,800 - $179,300 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Key activities for the Director include setting strategic direction for the global business, meeting revenue & profitability targets globally, building a high-performance marketing team, and working cross-functionally to integrate marketing strategies with quality, legal, regulatory, operations, clinical, medical affairs, reimbursement, and sales.
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Must possess a working knowledge of toxicology and preclinical regulatory requirements as they relate to the development and registration of medical devices and an eagerness to learn and develop scientific competence beyond their current skills.
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Familiarity with inventory control, OSHA, HACCP and other regulatory requirements. Regularly inspect facility for safety hazards and either resolve them or report them to the safety manager as appropriate.
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Coordinates compliance with regulatory agency requirements - OSHA, ADA, FMLA, CDC, MN Dept of. filing First Report of Injury and acting as liaison between team member, manager, health care provider.
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Other duties assigned by manager. Direct: Union and/or non-union warehouse on-floor associates (Loaders, Selectors, Receivers, Forklift drivers, etc.) PCQI certification a plus. Review performance, coach on productivity and safety targets, and deliver disciplinary action.
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Meyer Contracting Inc, is seeking qualified applicants for a Heavy Civil Estimator/Project Manager to join our team. We look forward to welcoming a talented Estimator/Project Manager to our team.
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We are seeking an energetic, dedicated professional to join our team in Maple Grove, MN as an Assistant Property Manager. 3+ years leasing or Assistant Property Manager experience. As an Assistant Property Manager, you will help us fulfill our mission of connecting residents to community.
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The department has an immediate opening for a Highway Project Manager who will perform various duties. These examples are not all-inclusive and are intended to be illustrative of the primary responsibilities of an Anoka County Highway Project Manager.
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Reporting to the Manager-Biological Safety Engineering, you will work cross-functionally and collaborate with R&D, NPD, CRO’s, Regulatory Agencies internal/external scientists and other stake holders.
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Highway/Heavy Civil Construction Project Manager. 3+ years Project Management/Construction Management experience; diversified Highway/Heavy Civil Construction experience preferred; Design-Build project experience a plus.
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regulatory affairs jobs Title: affairs manager Company: Jobget in Maple Grove, MN
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