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The Associate General Counsel provides a full range of legal advice and services related to health benefits law, insurance law, commercial law, contracts law and regulatory and compliance issues.. Juris Doctorate degree. Ability to provide timely and responsive legal support for business partners located in the Central and Eastern Time Zones. Relevant legal experience in health law, commercial healthcare insurance, Medicaid managed care, Medicare Advantage, litigation, contracting and/or healthcare provider legal support. We believe everyone–of every race, gender, sexuality, age, location and income–deserves the opportunity to live their healthiest life.
Join to apply for the Associate General Counsel - Remote role at UnitedHealthcare.. Juris Doctorate degree.. Ability to provide timely and responsive legal support for business partners located in the Central and Eastern Time Zones.. Relevant legal experience in health law, commercial healthcare insurance, Medicaid managed care, Medicare Advantage, litigation, contracting and/or healthcare provider legal support.. We believe everyone-of every race, gender, sexuality, age, location and income-deserves the opportunity to live their healthiest life.
Piper Health & Sciences is seeking an experienced and strategic Associate Director of Regulatory Affairs to lead regulatory planning and submission activities for biotechnology company in the Minneapolis, MN area. Serve as the regulatory lead for the tissue engineering program, advising on regulatory pathways and submission strategies. Stay current with evolving FDA regulations and guidance relevant to biologics and regenerative medicine. Strong understanding of FDA regulatory requirements and biologics development. Regulatory affairs, ind, investigational new drug, ectd, clinical research, biotechnology, biopharma, tissue, organ, stem cell, cmc, regulatory, biologics, fda, gcp, good clinical practices, regulatory writing, regulatory submissions
This unique opportunity is at a prestigious facility looking to hire a traveling therapist. This exciting area offers many recreational activities. As a premier travel therapy company, Host Healthcare offers top pay, excellent benefits, and personalized service. The ideal candidate for this position will be dedicated to providing patients with the highest level of service. The ideal candidate will also be knowledgeable in Medicare, Medicaid, and private insurance, as well as the ability to complete relevant insurance documentations.
The Regulatory Affairs Specialist plays a key role in supporting the registration and compliance of pesticide products across state and federal agencies.. Manage all state pesticide product registrations , including new applications, renewals, label amendments, and sales reporting.. Assist in interpreting and applying state, federal, and international pesticide laws and regulations.. Experience: 2+ years in Regulatory Affairs, Compliance, or a technical field (preferred).. Operates effectively within EOS, embracing clarity, accountability, and structured problem-solving
Job Summary: As a hematologist/oncologist at Allina Health, you will join a dedicated team passionate about providing transformative and enhanced care for individuals diagnosed with cancer each year in the Minneapolis/St. Paul area.. Accredited by ACS, CoC, NAPBC, and APEx in support of oncology quality, excellence, and stewardship. Allina Health Cancer Institute is seeking a board-certified/board-eligible medical oncologist/hematologist to join our growing practice.. Graduate of an accredited ACGME Hematology/Oncology fellowship training program required.. Over 20 oncology nurse navigators supporting patients and families throughout their journey.
An independent and not-for-profit system since 1924, Children's Minnesota is one system serving kids throughout the Upper Midwest at two free-standing hospitals, nine primary care clinics, multiple specialty clinics and seven rehabilitation sites.. The national honor recognizes the top diverse healthcare executives and organizations influencing public policy, care delivery, and promoting diversity, equity and inclusion in their organizations and the industry.. We also utilize extracorporeal membrane oxygenation (ECMO) and continuous renal replacement therapy (CRRT) when needed.. Our patient population requires complex care, including hemodynamic monitoring, critical medication management, maintenance of systemic perfusion and management of organ failure.. Children's Minnesota requires proof of COVID-19 vaccine, and as recommended by the Centers for Disease Control and Prevention (CDC), immunity to vaccine preventable infectious diseases, prior to employment.
Obtain necessary pre and post treatment vital signs and weight and perform vascular access evaluation pre- treatment Initiate dialysis treatment according to prescribed orders including blood flow (QB) and dialysate flow (QD).. Perform and record Pre and Post dialysis evaluation, weight, and vital signs with initial identification Responsible for calculating and entry of individual patients’ dialysis machine programming for Ultrafiltration (UF) goal; treatment time; and UF modeling as prescribed.. Ensure collection of lab specimens by appropriate lab courier.. Assists in assuring patient understanding or home dialysis products, benefits of home and how home dialysis can work for them.. Assist in assuring patient understanding of treatment options including demonstration of the peritoneal dialysis set-up.
Joining DaVita as Patient Care Technician (PCT) is an exciting opportunity to jump start your career in the health care industry!. We also have dedicated training to become a Facility Administrator, and training to become a Regional Operations Director.. To monitor patients before, during and after dialysis treatment including measuring and recording stats, patient observations, and hemodialysis machine setup.. Building long-term relationships with your patients who are suffering from end stage renal disease and are receiving treatment on average 3 times/week.. Health care experience a plus including: BONENT Certified, Certified Hemodialysis Technician (CHT), Certified Nursing Assistant (CNA), Certified Medical Assistant (CMA), or Phlebotomy certification.
The Executive Director (Registered Nurse, RN) in Hospice supervises all aspects of patient care, all activities of professional staff and allied health personnel, regulatory requirements compliance, financial performance, and quality assurance performance improvement activities for agency.. Immediately available (or has Alternate Designee) to be on-site during business hours or immediately available by telephone when off-site conducting agency business, available after hours as needed.. The Executive Director or designee RN, such as a Patient Care Manager, will receive daily reports on patients from staff.. Must be a licensed physician; licensed registered nurse; licensed social worker; or a Bachelor's degree college graduate with at least three (3) years of documented success in discipline/field of study and a minimum of one (1) year of full time experience in a hospice, home health, or other health care delivery system setting.. By applying, you consent to your information being transmitted by Nexxt to the Employer, as data controller, through the Employer's data processor SonicJobs.
Sholom offers a continuum of care ranging from senior apartment homes and assisted living to short-term rehab and skilled nursing care, hospice services, memory care, adult day services and meals on wheels. Sholom has built a reputation for excellence in providing high quality elder care, with both campuses being recognized as Five Star facilities for overall quality from the Centers for Medicare & Medicaid. The NAR/Care Specialist provides direct care to residents to maintain their highest practical physical, mental, and psychosocial well-being through quality care. Perform nursing care responsibilities, assisting residents with all NAR nursing cares in accordance with care plans and all safety protocols. Free membership to Sholom’s Fitness and Vitality Centers
They are at the core of who we are as a Star Tribune Top Workplace 2019-2024.. Collaborating with various departments, you'll assist in new product development and monitor supplier management to ensure ingredient excellence.. Required: Bachelor's degree in science, microbiology, food science, or equivalent experience. Desired: REHS, SQF Practitioner, Seafood HACCP, PCQI Certification, CFPM, Sensory Training, Labeling Training, Food Defense/Food Fraud, Lean Six Sigma, and/or equivalent experience. Ability to maintain compliance with USDA, FDA, HACCP, OSHA and all other regulatory agencies while complying with good manufacturing practices
Site: The Spaulding Rehabilitation Hospital Corporation. As a not-for-profit, we support patient care, research, teaching, and community service, striving to provide exceptional care.. Familiarity with electronic health records (EHR) systems and healthcare software.. The base pay information provided offers an estimate based on the minimum job qualifications; however, it does not encompass all elements contributing to your total compensation package.. The Spaulding Rehabilitation Hospital Corporation is an Equal Opportunity Employer.
Element has an opportunity for a Quality Assurance Coordinator who will be primarily responsible for assisting the Quality Manager with policies, practices, and systems for the Quality Assurance functions within Company operations.. This position also serves as the Export compliance and 5S Coordinator.. Coordinate and oversee 5S and Export Compliance programs which includes, at a minimum, monthly reporting and training events.. 2+ years of experience in a quality-related role within the TIC industry or a regulated technical environment.. From early R&D, through complex regulatory approvals and into production, our global laboratory network of scientists, engineers, and technologists support customers to achieve assurance over product quality, sustainable outcomes, and market access.
Looking for candidates local to the Maple Grove MN or St Paul MN area. The Global Regulatory Services (GRS) Quality Compliance Project Lead is responsible for supporting the RA procedure harmonization and related maintenance activities post harmonization. Regulatory processes have been harmonized across 6 Client medical device business units Support GRS own
Effortless documentation : Conversational and Dragon dictation.. PointClickCare, MatrixCare, and American HealthTech are the most commonly used facility EHR systems. Participating in Theorias Chronic Care Management, Transitional Care, RPM and other medical quality initiatives and programs. Leading the charge in healthcare innovation, Theoria Medical offers a unique blend of medical excellence and technological advancement, primarily serving the post-acute and primary care sectors.. Our extensive network includes multispecialty physician services and RPM, covering skilled nursing facilities across the country.
This includes strategies for gaining CE Mark under EU MDR. Coordinates, compiles, and submits US regulatory filings for new and modified products, including PMAs, PMA Supplements, pre-submissions, IDEs, 510(k)s, PMA & IDE Annual Reports. Demonstrated experience authoring/supporting a variety of regulatory submissions for US and EU, such as original PMAs, PMA Supplements, pre-submissions, IDEs, 510(k)s, and MDR Technical Documentation. Compensation for non-exempt (hourly), non-sales roles may also include variable compensation from time to time (e.g., any overtime and shift differential) and annual bonus target (subject to plan eligibility and other requirements).. Compensation for exempt, non-sales roles may also include variable compensation, i.e., annual bonus target and long-term incentives (subject to plan eligibility and other requirements).
The Regulatory Affairs Manager is responsible for leading regulatory functions and serves as management representative. Oversee, supervise, and provide direction in the following areas: Regulatory Strategy, Product Registration and Market Clearance, Device History Record Review, Employee Training, Design History File Maintenance, and Labeling. Assess the impact of changes on current clinical investigations and FDA filings. Bachelor's Degree or equivalent is required; Minimum of 10 years progressively responsible experience in the medical device industry is required; Minimum of 7 years within quality systems and/or regulatory compliance functions is required. This position is subject up to travel up to 15% of the time to include both domestic and international travel.
This person will report to the Global Regulatory Operations – Quality & Compliance Senior Manager.. These activities include: managing GRS CAPA tracker, quality review for verification, lead CAPA correction and corrective action delegated activities and tasks.. Develop, redline, and compile feedback on GRS owned procedure, work instructions, forms, and templates. Windchill experience (not required, but a plus). Delta Dental plan with 2 free cleanings and insurance discounts
We are the first publicly-traded biotech or pharmaceutical company to take the form of a public benefit corporation.. The cure for end-stage life-threatening diseases like PAH, PH-ILD, PF, and many others is an organ transplant, but only a small percentage of donated organs are available to address the vast need.. We believe an unlimited supply of tolerable, transplantable organs will eliminate the transplant waiting list and cure end-stage organ diseases for which transplant is not currently an option.. We are looking for a regular strategist who will advise on regulatory pathways, manage documentation and timelines, and support the preparation and execution of regulatory submissions for our whole tissue engineering program.. Must have written an IND and submitted it in ECTD format through the ESG portal