. Work Schedule and Additional Information Full time employment Work hours are 8 00 AM to 4 00 PM, Monday Friday, with 30 minute lunch. Work hours may be negotiable based on operational needs. Telework You may have the opportunity to telework, part time after the successful completion of the required probationary period. In order to telework, you must have a securely confi

Analytics Advisory Associate Manager, L8 Location Burlington, NJ Accenture is a leading global professional services company that helps the world's leading businesses, governments and other organizations build their digital core, optimize their operations, accelerate revenue growth and enhance citizen services creating tangible value at speed and scale. We are a talent an

. Work Schedule and Additional Information Full time employment Work hours are 8 00 AM to 4 00 PM, Monday Friday, with 30 minute lunch. Work hours may be negotiable based on operational needs. Telework You may have the opportunity to telework, part time after the successful completion of the required probationary period. In order to telework, you must have a securely confi

The Regulatory Affairs Specialist drafts, submits and gains clearance for 510(k) submissions, and approval for IDE/PMA submissions to the Food and Drug Administration (FDA) for class II and class III products. This position entails development of FDA submissions, requires working knowledge of products under review and of relevant regulations and guidance documents. This i

. Work Schedule and Additional Information Full time employment Work hours are 9 00 AM to 5 00 PM, Monday Friday, with a 30 minute lunch. Work hours may vary based on operational needs. Telework You may have the opportunity to telework, part time after the successful completion of the required probationary period. In order to telework, you must have a securely configured

Coordinates and prepares document packages for regulatory submissions for new and mature products, ensuring compliance with local and regional registration requirements. Compiles all materials required in submissions, license renewal and annual registrations. Recommends changes for labeling, manufacturing, marketing and clinical protocol for regulatory compliance. Monitor

BNY Mellon is a global investments company dedicated to helping its clients manage and service their financial assets throughout the investment lifecycle. Whether providing financial services for institutions, corporations, or individual investors, BNY Mellon delivers informed investment management and investment services in 35+ countries. As of July 18, 2023, BNY Mellon

The Compliance Manager works with the Director of Compliance and Chief Compliance Officer to support our Global business on compliance matters relating to adherence to relevant policies, codes, laws, and regulations impacting business operations. The Compliance Manager will assist with various aspects of our compliance program, including compliance training, auditing and

Primary Office Location 503 Martindale Street 4th Floor. Pittsburgh, Pennsylvania. 15212. Join our team. Make a difference for us and for your future. Position Title Contact Center Quality Assurance Analyst Business Unit Retail Operations Reports to Manager of Contact Center Quality Assurance Position Overview This position is responsible for monitoring Primary Contact Ce

Senior Associate, Data Management & Quantitative Analysis Bring your ideas. Make history. BNY Mellon offers an exciting array of future forward careers at the intersection of business, finance, and technology. We are one of the world's top asset management and banking firms that manages trillions of dollars in assets, custody and/or administration. Known as the "bank of b

Senior Regulatory Affairs Associate Experience Biologic CMC 5+ years of experience Supported the CMC activities related to Vaccine/Biologic manufacturing and control including authoring of submission dossiers related to new application, post approval variations Understanding of EU/CA/WHO/US regulations & guidance allowing appropriate review and compilation of data to appr

Participates in and identifies specific tests while executing test scenarios for unit, process, function, system integration, regression and acceptance testing. Defines criteria for testing, analyzes results of testing sessions and presents testing results to project stakeholders. Reviews applicable requirements in order to develop complex test cases, scenarios and script

include Works individually and as a team to engage with potential and active program participants Assists during direct service delivery to facilitate participant flow and throughput Assists program participants both during direct service delivery and telephonically in identifying personal recovery goals, assisting in setting objectives for each goal, and determining inter

The Lead Regulatory Affairs Specialist leads the preparation of document packages for regulatory submissions for new and sustaining enhanced technologies, software enabling and robotics systems within the Surgical Intelligence (SI) portfolio, to ensure compliance with local and regional registration requirements. The Lead Specialist will be responsible for coordinating pr

Coordinates and prepares document packages for regulatory submissions for new and mature products, ensuring compliance with local and regional registration requirements. Compiles all materials required in submissions, license renewal and annual registrations. Recommends changes for labeling, manufacturing, marketing and clinical protocol for regulatory compliance. Monitor