Liquidity Regulatory Reporting Analyst/Manager Location: NYC, NY (Onsite position / No Remote work) Longterm contract As a Liquidity Manager specializing in LCR, 2052a, NSFR, Governance, and Controls. Nice to have: Extensive expertise in leveraging tools such as Axiom, Tableau, and SQL to ensure financial institutions maintain optimal liquidity positions while adhering to regulatory requirements.
Liquidity Reporting Manager Location: NYC, NY (Onsite position / No Remote work) Longterm contract Required Skills: Deep understanding of Liquidity Coverage Ratio (LCR), 2052a, Net Stable Funding Ratio (NSFR), and governance frameworks. Generate/Produce daily consolidated FR 2052a results
Who we are: Bloomberg is known for keeping our clients ahead of the competition, and it's no secret that regulation has become the name of the game in recent years. Following increased regulations around the world, the Post Trade group was created to capitalize on opportunities to better support our clients' regulatory needs. The Enterprise Reporting team is responsible for providing a product to our clients that takes away the complexity across various regulations. The Bloomberg Regulatory Repo
We are the leading provider of professional services to the middle market globally, our purpose is to instill confidence in a world of change, empowering our clients and people to realize their full potential. Our exceptional people are the key to our unrivaled, inclusive culture and talent experience and our ability to be compelling to our clients. You'll find an environment that inspires and empowers you to thrive both personally and professionally. There's no one like you and that's why there
About the Role: Grade Level (for internal use): 13 The Team: This is a commercial position within S&P Global Market Intelligence, Regulatory Compliance Division. This position will report into the of Commercial Head Managed Services but work closely with the Sales, Operations, Technology / Product team across Regulatory Compliance. Responsibilities and Impact: Our comprehensive services bring greater transparency to financial markets, helping to reduce risk and create opportunity. We provide ex
About this role: Wells Fargo is seeking a Software Engineering Senior Manager (Global Regulatory Reporting) as part of the Wholesale Operations Technology (WOT) Organization. This role will be accountable for the Wells Fargo Global Transaction Reporting ecosystem and will work closely with the Regulatory Reporting Product owner and team. This role will oversee the work to support three global regions (Americas, EMEA and APAC). Critical to this role will be a strong understanding of OTC products
Company Description AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on Twitter, Facebook, Instagram,
Responsibilities: Hands on development of quality (i.e. readable, performing and supportable) AXIOM Code, delivering the functionality detailed in the technical specifications Hands on development of Autosys, Unix, and Perl scripts, delivering the functionality detailed in the technical specifications Development and review of PL/SQL code to support data sourcing into Axiom. Review FRD documents to ensure the functional requirements are well understood. Review PL/SQL codes to handle perform
Software Guidance & Assistance, Inc., (SGA), is searching for a Regulatory Affairs Senior Manager for a FULL TIME assignment with one of our premier Pharmaceutical Services clients in Hawthorne, NY. Responsibilities: US Agent for all Firm's products, responsible for communication between the FDA and manufacturing sites. Communicate and follow-up status with FDA for any Chemistry, Bioequivalence and Patents issues and correspondences on both pending and approved applications Lead, guide and t
Job Title: Senior Regulatory Affairs Specialist (Medical Devices) Location: Remote Duration: Long term contract Job Description: -Subject Matter Expert for Class II and Class 510(K) submission. -Hands on experience with 510(k) authoring, submissions, and communicating with the FDA. -Hands on experience with software as a Medical Device (SaMD) and validation requirements and applicable consensus standards. Key Responsibilities- -Authoring US FDA 510(k) submission using eSTAR submission tool.
Please note that this is a 1 year contract position. HIGHLIGHTED SKILLS: - Role can be 100% REMOTE - May travel for a possible mandatory meeting onsite (Raritan, NJ) for 1-2 days, not very often at all - Bachelors Degree required - Pharmacovigilance experience needed - Must be flexible / adaptive - Must be able to problem solve, and know when to ask for help - Working within the Global Environment / Global Teams - Regulatory Affairs experience - MAIN ASPECT OF ROLE: Support Aggregate Tracking p
Technical Writer Location: Remote work Duration: 7 months Job description: We are seeking a Technical Writer to join our team and support the IT Operations project tracks within the ISO initiative. In this role, you will collaborate closely with the IT Ops project management team to conduct working sessions and engage with external stakeholders across various ISO tracks. The immediate focus of this position is to work collaboratively with the Infrastructure and Technology, IT Business Engagement
