Join our team as a night shift, full-time, Medical Surgical, 4th-West Patient Care Technician (PCT) in Westwood, NJ.. Hackensack Meridian Pascack Valley Medical Center is a 128-bed, full-service, acute-care community hospital with a new emergency department, a state-of-the-art maternity center, a women's imaging center, and an ICU.. The Patient Care Technician plays a vital role in the healthcare delivery setting often having more patient contact than any other team member, including doctors and nurses.. Current Basic Life Support (BLS) Certification by the American Heart Association (AHA) or the American Red Cross (ARC).. Certified Nursing Assistant (CNA)
RN MDS Coordinator. Familiar with Reimbursement system of Medicare, Medicaid & Case Management. Preferred Skilled Nursing Facility Experience as an MDS Nurse. Touchstone Emergency Assistance Foundation Grants. Compassionate team members are the key to revealing our vision to be the leading post-acute healthcare solution in the markets we serve.
BS/BA, preferably in regulatory affairs or science, Masters in Regulatory Affairs preferred.. Five years of direct work experience in medical device regulatory affairs is required. Excellent organizational, technical writing and communication skills. Experience with various types of preclinical testing, such as biocompatibility, electrical safety, and useability.. Lean Six Sigma experience and/or certification
Wellington Regional is proud to have provided high quality healthcare services to the residents of Palm Beach County since 1986.. We are proud of our robust continuing education options and opportunities for skills diversification and career advancement as a PCT with UHS. We want to help you succeed and grow in your profession and enjoy a sense of belonging and trust that comes through your expanding experience.. About Universal Health ServicesOne of the nation’s largest and most respected providers of hospital and healthcare services, Universal Health Services, Inc. (UHS) has built an impressive record of achievement and performance.. Qualifications Patient Care Technician (PCT) Job Requirements:High school graduate or equivalent preferred.. Computer skills, order entry and ADT functionRole and ResponsibilitiesPerforms various customer care activities and related services in the patient care area including monitoring and interpreting cardiac telemetry rhythm strips, receptionist and secretarial duties, and patient care tasks.
Whether your abilities are in direct patient care or one of the many other areas of healthcare administration and support, everyone at Parkland works together to fulfill our mission: the health and well-being of individuals and communities entrusted to our care.. By joining Parkland, you become part of a diverse healthcare legacy that’s served our community for more than 125 years.. Maintains, updates, and utilizes knowledge of sanitation, infection control, safety, supplies and equipment usage to optimize customer care and services.. Parkland Health and Hospital System prohibits discrimination based on age (40 or over), race, color, religion, sex (including pregnancy), sexual orientation, gender identity, gender expression, genetic information, disability, national origin, marital status, political belief, or veteran status.. As part of our commitment to our patients and employees’ wellness, Parkland Health is a tobacco and smoke-free campus.
Regulatory Affairs Specialist (IVDR).. On behalf of our client a medical device company we are seeking for a Regulatory Affairs Specialist to support in their transition efforts for the EU’s In Vitro Diagnostic Regulation (IVDR). Update the labeling conversion tracking log using manufacturing schedules, fill dates, lot numbers, and change request information. Bachelor’s degree in Biochemistry, Biology, Medical Technology, or related field. 3+years of experience in Regulatory Affairs, Quality Assurance, R&D, Manufacturing, or Project Management within the IVD industry.
On-Board Scientific is hiring a Regulatory Affairs Specialist in. Title: Regulatory Affairs Specialist. Bachelor’s degree in Chemistry, Biology, Toxicology, or a related field. Familiarity with OSHA, TSCA, RCRA, and Export regulations is desirable. The On-Board Family of Companies conducts operations through its Corporate Headquarters located in East Windsor, NJ along with Regional Offices in New Castle, DE and Wake Forest, NC. On-Board’s Mission is to provide “Flexible Service by applying the talents of our people, work processes and technology to meet our clients’ expectations in a Safe, Responsible and Dependable manner.”
Work Arrangement: Fully remote, travel 25% - 50% (at most). Position Summary: Telephonic outreach to members, addressing gaps in care, barriers to care, and improving member experience.. Telephonic outreach to members, addressing gaps in care, barriers to care i.e., transportation, offering in-home test kits for gap closures.. Bachelor’s Degree in Healthcare, Public Health, Registered Nurse, Psychology, Social Work, Health Administration, or related health field or equivalent work experience.. Preferred: Associate Nursing Degree, Project Management/Lead, Case Management.
REGULATORY AFFAIRS MANAGER The Opportunity The function of a Regulatory Affairs Manager is to combine knowledge of scientific, regulatory and business issues to enable products that are developed, manufactured or distributed to meet the required legislation.. Experience with 510(k) applications, IDEs, PMA or PMA supplements and US device regulations and / or experience with EU and other international medical device regulations and submissions.. Bachelor's degree in science (biology, chemistry, microbiology, immunology, medical technology, pharmacy, pharmacology), math, engineering, or medical fields.. Strong working knowledge of regulatory requirements for US, EU (EU MDR), and other international geographies.. Certification is a plus (such as RAC from the Regulatory Affairs Professionals Society).
Join to apply for the Regulatory Affairs Manager role at American Vanguard.. AMVAC, an American Vanguard company, has an opportunity for a Regulatory Affairs Manager with EPA experience. We focus on four innovation platforms: Proven Chemistries, Precision Agriculture, GreenSolutions, and Sustainability Solutions for plant and soil health. The Regulatory Affairs Manager will be appointed to participate as an active member of Industry regulatory or scientific committees and will have the opportunity to network with Industry peers.. Get notified about new Regulatory Affairs Manager jobs in Newport Beach, CA.
The Research Nurse II is responsible for providing nursing technical expertise and overall execution of clinical trials, with an emphasis on later phase (II-III) clinical trials and an introduction to phase I trials.. The incumbent will be expected to follow Good Clinical Practice (GCP) and all organizational policies and procedures for patient safety and data integrity, including but not limited to the Institutional Review Board (IRB), Food & Drug Administration (FDA), Code of Federal Regulations (CFR), and International Conference on Harmonization (ICH) guidelines.. Utilizes nursing education to contribute to study start-up activities, including site initiation visits, protocol review of feasibility and suggestions for revision, study and clinical staff training.. The Masonic Cancer Center (MCC) is an NCI-designated Comprehensive Cancer Center dedicated to cancer research, education, and patient care for the citizens of Minnesota and the surrounding region.. At the University of Minnesota, we are proud to be recognized by the Star Tribune as a Top Workplace for 2021, as well as by Forbes as Best Employers for Women and one of America's Best Employers (2015, 2018, 2019, 2023), Best Employer for Diversity (2019, 2020), Best Employer for New Grads (2018, 2019), and Best Employer by State (2019, 2022).
Wellington Regional is proud to have provided high quality healthcare services to the residents of Palm Beach County since 1986.. wellingtonregional.com Benefits for our Patient Care Technician (PCT) include: Tuition Assistance Loan Forgiveness Tuition savings to continue your nursing education In-house Nurse Residency Transition-to-Practice Orientation (20 CEUs) Career development opportunities across UHS and our 300+ locations!. Diverse programming to expand your experience HealthStream online learning catalogue with plenty of free CEU courses Competitive Compensation & Generous Paid Time Off Excellent Medical, Dental, Vision and Prescription Drug Plans 401(K) with company match and discounted stock plan Pet Insurance SoFi Student Loan Refinancing Program •More information is available on our Benefits Guest Website: benefits.. uhsguest.com If you would like to learn more about the PCT position before applying, please contact Kenra Layton, Nurse Recruiter at Lorkenra.. Computer skills, order entry and ADT function Role and Responsibilities Performs various customer care activities and related services in the patient care area including monitoring and interpreting cardiac telemetry rhythm strips, receptionist and secretarial duties, and patient care tasks.
Join to apply for the Regulatory Affairs Manager role at Shell Energy. Actively participate in developments and proceedings before federal agencies including FERC, CFTC and DOE. Monitor federal and state legislative activity and coordinate with Corporate Relations teams to ensure messaging alignment and timely distribution of information about any developments that impact company positions or operations.. Minimum of 5 years industry experience in energy regulation primarily in U.S. and specifically with federal agencies, i.e. FERC, CFTC, DOE. We are excited to play a key role in the move to net carbon emissions while providing the oil and gas needed by society for many decades to come.
We have an unwavering commitment to safely and reliably deliver electricity and natural gas to millions of people.. Manages the development and execution of regulatory policies and strategies in collaboration with internal stakeholders that support CNP’s corporate strategy, goals and objectives with participation of the appropriate CNP groups or departments.. Partners with a cross functional team for the development of recommendations to management for the need and timing of general rate cases and major filings to support CNP’s corporate strategy, goals and objectives.. Maintains good working relationship with regulators, their staffs, internal colleagues including legal, government affairs, rates groups, and customers.. Access to discounts at fitness clubs and an on-site wellness center at our headquarters in Houston
We are seeking a Regulatory Affairs Manager to join our team to lead and broaden the impact of our ongoing regulatory affairs efforts across the United States.. Prepare and implement annual (and ad-hoc) strategic planning to detail Scale’s efforts to improve state and ISO/RTO markets for microgrids, including renewable energy, dispatchable generation and battery storage deployment.. 5+ years in regulatory affairs, energy policy, or market strategy roles, ideally within renewable energy, utilities, or microgrids.. Familiarity with distributed energy technologies (e.g. microgrids, energy storage) and utility program dynamics in one or more key markets is preferred.. Scale Microgrids (“Scale”) is a fully integrated distributed energy platform focused on designing, implementing and financing innovative distributed clean energy solutions.
WHOOP is seeking a Regulatory Affairs Manager (Medical Devices) to navigate and manage regulatory affairs for Medical Device Software in the US. In this role, you will work with the WHOOP Medical Device Team to act as a champion of U.S. Regulatory activities throughout the medical device lifecycle.. As a Regulatory Affairs Manager, you will be responsible for various regulatory & quality functions, such as leading regulatory submissions, implementation of quality system processes, collaborating with the WHOOP Medical Device Team throughout the product development process, and ensuring compliance with the Quality Management System (QMS).. Implement post-market surveillance, including complaint handling, adverse event reporting (MDR), and field actions. Bachelor’s Degree in Life Sciences, Regulatory Affairs, Biomedical Engineering, or related field, or equivalent practical experience. Nice to Have: Experience with Consumer Wearable Products, General Wellness Products, Digital Health or Mobile Medical Applications
The Wellness Pet Company crafts and produces premium natural pet food, treats, dental chews, and supplements.. We believe that natural, premium nutrition focused on proven health outcomes is the foundation of creating mutual wellbeing for pets and their families.. We are currently seeking a Regulatory Affairs Associate to join our team.. Research export requirements for animal products to ensure regulatory compliance in market.. BS in a technical discipline (Food Science, Animal Science, Nutritional Science, or similar discipline).
Manages regulatory affairs, including product registrations, licensing (CRHB, SS&DRs, CMDR, RMLs), export control, and submissions for international markets.. Experience: 5+ years in medical device or pharmaceutical regulatory affairs, including 5+ years of management experience and 5+ years preparing regulatory submissions (FDA, EU MDR, international).. Proficiency in MDSAP, MDD, EU MDR/IVD, FDA, QSR/QMSR, ISO standards.. Experience with design control, manufacturing, process development, QA/QC.. Proficient in Microsoft Office Suite, ERP systems (e.g., Microsoft Dynamics), and flowcharting programs.
If you can do all of this artfully displaying passion and humility, look no further than the Medical Sales Representative role at Biocodex!. The Medical Sales Representative will report to the Senior Manager, Medical Sales USA. The primary function will be to focus on growing both the current book of business and developing new selling relationships with our HCP customers.. The Medical Sales Representative Role is responsible for identifying key opportunities within their territory by 1) increasing HCP understanding, advocacy, and recommendations for Florastor via product education and as a result, 2) grow current sales while simultaneously creating new business for revenue acceleration.. The Medical Sales Representative will need to have a clear understanding of the science behind Florastor, and what makes it both unique and compelling to medical professionals & consumers alike in the U.S. marketplace.. At the same time, the Medical Sales Representative must be comfortable in a selling environment where many of their competitors are larger companies offering significant sampling and high levels of direct-to-consumer marketing.
Our Clinical Research and Pharmacovigilance team push the boundaries of global healthcare through research and innovation. As a Pharmacovigilance (PV) Senior Specialist, you will be responsible for adverse event management including aggregate and individual case safety report (ICSR) health authority submissions and compliance monitoring. Demonstrated solid pharmaceutical industry experience in Pharmacovigilance/Drug Safety.. Work with a passionate Pharmacovigilance and Regulatory Affairs Team. You can put your empathy, creativity, digital mastery, or scientific genius to work in collaboration with a diverse group of colleagues who pursue and bring hope to countless people who are battling some of the most challenging diseases of our time.