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Axiom Developer/Regulatory Reporting Consultant

United IT Solutions

Remote

Full-time

Role: Axiom Developer/Regulatory Reporting Consultant Location: Remote Job Type: Fulltime Job Description Design and develop Data Sources, Data Models, Shorthands, Portfolios, Aggregations, Free Form and Tabular Report and workflows using AXIOM controller view tool based on Regulatory report requirements. Development and review of PL/SQL code to support data sourcing into Axiom understanding end to end data flow from DB to AxiomStrong hands-on development experience with ETL jobs and creating t

Policy Legal: Regulatory Contractor

TalentBurst

San Francisco, California, USA

Full-time

Policy Legal: Regulatory Contractor 40 hrs./week June-July 2024 (2 months) Duties: The Legal team embodies the company's innovative and entrepreneurial spirit. We continue to break new ground in matters of policy and law around the world. Where some see obstacles, we see opportunities to find creative and practical solutions. We're an adventurous, fast-moving group that supports many functions and teams across the company. We are looking for candidates interested in law and policy who can as

Sr. Regulatory Operations Specialist

Zachary Piper Solutions, LLC

Philadelphia, Pennsylvania, USA

Full-time

Piper Companies is currently seeking a Sr. Regulatory Operations Specialist to support a growing and innovative cell and gene therapy company in Philadelphia, PA (Hybrid Schedule). Responsibilities for the Sr. Regulatory Operations Specialist Coordinate diverse regulatory submissions by collaborating with internal teams and stakeholders, and develop content plans for IND & CTA dossiers. Lead interactions with external publishing teams to compile IND or CTA submissions, including reports and

Regulatory and Client relationship management

Net2Source Inc.

New Jersey, USA

Full-time

Role: Regulatory and Client relationship management Work Location: New Jersey Or Chicago, IL Hire Type: Fulltime 1.The candidate should be Assertive, 2.Situational Leadership, 3.Process Mapping Competency 4.RAPS (or equivalent) Certification is nice to have 5.1 2 years of business development and client relationship management desirables Experience in 2-3 additional LS specific domain areas would be desirable "Plan and Execute Regulatory Transformation project with excellent presentation skills,

Regulatory Affairs Specialist, Cell & Gene Therapy

Zachary Piper Solutions, LLC

Philadelphia, Pennsylvania, USA

Full-time

Piper Companies is currently seeking a Regulatory Affairs Specialist, Cell & Gene Therapy for an opportunity in Philadelphia, Pennsylvania (PA), to join an innovative biotechnology company creating life-saving cell therapies. Responsibilities of the Regulatory Affairs Specialist, Cell & Gene Therapy Coordinate and manage timing for regulatory submissions, collaborating with internal teams and stakeholders. Oversee external publishing coordination for IND/CTA submissions and related documents.

Liquidity Regulatory Reporting Manager

Intraedge

New York, New York, USA

Contract

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.

Program Manager (Liquidity /Regulatory Reporting)

Intraedge

New York, New York, USA

Contract

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

Financial Regulatory Reporting Consultant

Shimento, Inc.

Dallas, Texas, USA

Contract

Financial Regulatory Reporting Consultant Location:- Dallas, TX, NJ, Phoenix AZ, South Carolina, Minneapolis, MN and Los Angeles, CA Onsite 3 days Hybrid Duration- 12 Months Required Qualifications: 4+ years of Finance, Accounting, Financial Reporting experience, or equivalent demonstrated through one or a combination of the following: work experience, training, military experience, education. Desired Qualifications: Demonstrated knowledge of Regulatory FR Y-14, Schedule RC-H and related Regula

Regulatory Affairs Associate

Apex Systems

Mountain View, California, USA

Full-time

Job#: 2027155 Job Description: Client: IRIDEX Position: Regulatory Affairs Associate Location: Mountain View, CA Estimated Duration: The client approximates that this project may last up to 5 months. However, there is no guarantee of employment for any length of time. Pay Rate Range: $35 - $45/hr IRIDEX Corporation is a medical device manufacturer and operates in a global regulated environment (e.g. FDA). Regulations include (but are not limited to) FDA 21 CFR 820, EN ISO 13485, Health Cana

Regulatory Specialist (US)

Dexian DISYS

Erlanger, Kentucky, USA

Contract

Job Title - Regulatory Specialist Duration -10+ Months Location - Erlanger KY 41018 (Hybrid 3- Days Onsite,2 days Remote) Roles and Responsibilities: Regulatory Specialist to support the business /operations productivity to communicate with vendors technical regulatory inquiries, documentation needs and data maintenance and interpretation. A working knowledge of FDA food regulations and relevant product design status such as GM\BE, Allergens, GRAS, Vegan, Natural, Kosher, Organic, Halal, Nutr

Global Regulatory lead - Associate Director

Dizer Corp

Millburn, New Jersey, USA

Contract, Third Party

Title - Global Regulatory Lead - Associate Director Location - Short Hills, NJ Develop global regulatory strategy for Oncology products in development and through life cycle management taking into account all relevant guidance, commercial needs, and company objectives. Responsibilities: Develop global or US regulatory strategy for Oncology products in development and through life cycle management, considering all relevant guidance, commercial needs, and company objectives. Develop strategic dir

Regulatory Affairs Specialist

Ledgent Technology

Irvine, California, USA

Contract

Summary: The main function of a regulatory affairs specialist is to complete and maintain regulatory approvals and clearances of assigned products. Key Responsibilities: * Create regulatory submissions (exercising judgment to protect proprietary information) for finalization and submission by OUS EW affiliates; track timelines and document milestone achievements, participate in developing regulatory strategy, prioritize submissions with operating plans as well as ensuring alignment with KOD in c

Regulatory Remediation Project Manager

Software Guidance & Assistance

Tampa, Florida, USA

Contract

Software Guidance & Assistance, Inc., (SGA), is searching for a Regulatory Remediation Project Manager for a contract assignment with one of our premier financial services clients in Tampa, FL, Irving, TX, New York, NY or Jersey City, NJ. Responsibilities : Will be a key member of the Procurement and Third-Party Management Operational Excellence team within the firm supporting engagements necessary to deliver against transformation and regulatory priorities. Projects will vary in size, durat

Vice President, Regulatory Data Governance Lead

BNY Mellon

Pittsburgh, Pennsylvania, USA

Full-time

Vice President, Regulatory Data Governance Lead 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 banks" - 97% of the world's top banks work with us as we lead and serve our customers into the new era of digital. With over 239 years

Regulatory Affairs Manager - Neuromodulation (on-site)

Abbott Laboratories

Plano, Texas, USA

Full-time

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries. Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. Yo

Axiom Developer for the Regulatory Reporting Team

Kaizer Software Solutions

Jersey City, New Jersey, USA

Contract

Hi, Greetings from Kaizer Software Solutions Position: Axiom Developer for the Regulatory Reporting Team Location:Jersey City, NJ (Hybrid mode of working 2 days a week from office) Type: Contract Job Description: Responsibilities: Working experience of regulatory reporting for APAC/EMEA regulators.Experience in solution implementation with Axiom scripting language.To have knowledge on Controller View objects like Data Sources, Data model, Aggregation, Shorthand, Portfolio, Modify models, Freef

Senior Regulatory Affairs Specialist (Medical Devices)

ApTask

Remote

Contract

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.

Technical Safety & Regulatory Compliance (TSRC) Student Program - Environmental Compliance Engineer

Stellantis

Auburn Hills, Michigan, USA

Full-time

The Stellantis Technical Safety and Regulatory Certification (TSRC) S tude nt P rogram P articipant will have the opportunity to work in the exciting world of regulatory certification and compliance. This role perform s certification and compliance testing and analysis to support emissions and OBD (Onboard Diagnostics) certi fication for all vehicles sold in the United States and Canada . The student may be assigned different responsibilities in multiple rotations . These assignments will provid

Manager Regulatory Affairs

Abbott Laboratories

Des Plaines, Illinois, USA

Full-time

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries. About Abbott Abbott is a global healthcare leader, creating breakthrough science to improve people's health. We're always looking towards the future

Regulatory Affairs Manager - Structural Heart (on-site)

Abbott Laboratories

Saint Paul, Minnesota, USA

Full-time

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries. About Abbott Abbott is a global healthcare leader, creating breakthrough science to improve people's health. We're always looking towards the future