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Experience as a Program Manager at Medtronic or medical device industry in Clinical Research or Clinical/Medical Affairs, Regulatory, Quality, Engineering, Health Care. Work across the Medtronic Clinical and Regulatory enterprise and adjacent functional partners by offering a variety of services: Program & Project Management, Process Improvement, Value Stream Excellence, Project Management Training & Coaching, Strategic Planning Facilitation, Council/COE Facilitation, Kaizen Facilitation, and MPS/Green Belt coaching.
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Administer the process of applying for permits related to mining activity, including coordination with management, legal staff, and local/state regulators, across all regulatory programs, including air quality, water rights, process and stormwater discharge, Army Corps/WACA/TEP/LGU floodplain and wetlands, and endangered species.
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Support the Companys general legal needs, including commercial and government contracts, advertising, regulatory compliance, international product distribution and litigation management. The successful candidate requires a strong background in developing and managing IP legal strategy, ideally as in-house counsel for a company in the CPG space.
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Responsibilities Management of the Coordination with City, County, and Federal agencies to maintain regulatory compliance for entitlements and environmental issues. #CB #LI-DT1 Type Regular Full-TimeManagement of the Coordination with City, County, and Federal agencies to maintain regulatory compliance for entitlements and environmental issues.
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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.
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Identify optimal reimbursement pathways for portfolio pipeline (coding/coverage/payment) Collaborate with new product development teams and clinical/regulatory colleagues to ensure health economics and market access needs are incorporated into product development plans, clinical trials and regulatory strategies Participate as contributing member on cross-functional evidence planning teams.
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Regularly interact with the Regional Environmental Manager (REM), regulatory agencies, and division associates. Regularly interact with and assist division associates to achieve storm water and air quality regulatory compliance.
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Facilitate communication and exchange of documents between stakeholders (e.g., internal personnel such as Regulatory Affairs, R&D Engineering, Clinical Engineering, A&P and Marketing, Library Services, Quality Engineering, Post-market Surveillance Group, Clinical Affairs, Risk Management, Program Management, as well as external vendors such as CROs, Medical Writers and Physician Reviewers.
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Work to Corporate Regulatory/Product Stewardship team and provide updates as needed, Support all Company initiatives as identified by management and in support of Quality Management Systems (QMS) and other regulatory requirements.
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Adheres to Integer Core Beliefs and all safety and quality requirements including, but not limited to: Quality Management Systems (QMS), Environmental Management Systems (EMS), U.S. Food and Drug Administration (FDA) regulations, Company policies and operating procedures, and other regulatory requirements.
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The Regulatory Affairs Specialist will develop strategies and submissions for projects and issues related to regulatory documents, global submissions, investigations, product development planning, and regulatory agency interaction for blood products and biologics.
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Stay compliant with DOT/FMCSA and OSHA regulations including completion of training activities as required by DSG policy and/or regulatory authorities. Dakota Supply Group (DSG) is seeking an Overnight CDL Class A Delivery Driver in our Plymouth, MN location.
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Strong knowledge in all areas of import / export, regulatory and logistics management. Responsible for import logistics system team including carrier contract negotiations and import customs clearance.
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Ensures members of this team maintain compliance with internal policies related to admissions, assessment and intake processes and procedures, as well as compliance with requirements set forth by the MN Department of Health for hospital licensure, The Joint Commission, CMS, and other regulatory bodies.
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Job Summary The Maintenance Technician I supports the FedEx Ground Industrial Maintenance for material handling to complete preventative and predictive maintenance and repair of material handling systems.
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regulatory affairs jobs Title: regulatory affairs specialist Company: Jazz Pharma in Osseo, MN
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