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Contract - Financial Business Analyst with Regulatory Reporting Experience

DATASYS CONSULTING & SOFTWARE INC

Remote

Full-time

JOB DESCRIPTION: CONTRACT ON W2 (NO C2C) Title: Financial Business Analyst with Regulatory Reporting Experience Location: New Jersey Work Mode: Remote We are seeking a highly skilled and motivated Financial Analyst specializing in regulatory reporting to join the team. The ideal candidate will have a strong understanding of financial principles, regulatory requirements, and reporting standards. The role involves analyzing financial data, ensuring compliance with regulatory guidelines, and provid

AXIOM REGULATORY REPORTING

Tabono Technologies INC.

Hanover, New Jersey, USA

Contract, Third Party

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

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.

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 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

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 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

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

Regulatory Affairs Manager - Electrophysiology

Abbott Laboratories

Plymouth, 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. 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

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 Project Manager - Structural Heart

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

Financial & Risk Regulatory Reporting - Project Manager

Dexian DISYS

Concord, California, USA

Contract

Financial & Risk Regulatory Reporting - Project Manager Concord, CA: Locals Only! 9 + Months $70 - $71/HR Onsite Day 1: Hybrid Model: 3 Days Onsite Per Week! Description: As part of the Finance & Risk Regulatory reporting function within the Commercial Banking. Candidates will be interested in joining this team if they want to work in an exciting area where Data meets Banking. The Commercial Banking data team supports CB initiatives by providing data strategy, governance and enablement in sup

CMC 2 Regulatory affairs

Hectadata LLC

Jersey City, New Jersey, USA

Contract, Third Party

Greetings from Hectadata, LLC. We are hiring for the position of CMC 2 Regulatory affairs Please find the below Job Description. If you are interested in this position, kindly submit your applications via Dice. Job Title: CMC 2 Regulatory affairs Location: JFK Parkway, NJ Job Description: We are inviting applications for the role of CMC 2 Regulatory affairs. Responsibilities: Well versed in performing CMC compliance activities including Gap Analysis; assessment for Annex 3 comparative table with

Regulatory Data Governance Lead :Concord, CA hybrid onsite 3 days every week

Hirex

Concord, California, USA

Contract

HireX is the North American leader in staffing, recruitment, and HR Services. A key player in the recruitment and staffing market, HireX provides unrivaled expertise in matching North America's top talent with the most sought-after North American employers. Regulatory Data Governance Lead Concord, CA hybrid onsite (3 days/week; remote 2 days/week) 12+ months Contract Video (Teams) Interview Data governanceLoans, Lending and/or Commercial Banking area of dataLeading data transformational and reme

Regulatory Data Governance Lead

Activesoft, Inc.

Concord, California, USA

Contract

Job Title :- Regulatory Data Governance Lead Location :- Concord, CA hybrid onsite (3 days/week; remote 2 days/week) 12+ months Required: 7+ years in data governance with at least 4 years in Loans, Lending and/or Commercial Banking areaMust have experience leading data transformational and remediation initiativesExperience working within the Data Product Backlog assisting with the roadmapStrong experience within regulatory reporting (eg: FRY 14Q, FR 2052a)Day to Day: Act as a key data subject

Senior Regulatory Affairs Specialist (Robotics & Digital Solutions) - Ethicon, Inc.

Johnson & Johnson

Cincinnati, Ohio, USA

Full-time

Description Robotics & Digital Solutions, part of the Johnson & Johnson Medtech Surgery, is recruiting for a Senior Regulatory Affairs Specialist . The preferred location for this role is within a commutable distance of Cincinnati, OH however candidates within commutable distance of Santa Clara, CA or Raritan, NJ will also be considered . This role will work a Flex/Hybrid schedule with 3 days per week on-site. About Johnson & Johnson At Johnson & Johnson, we believe health is everything. Our

Manager Global CMC Regulatory Affairs

Johnson & Johnson

Raritan, New Jersey, USA

Full-time

Description Johnson & Johnson Innovative Medicine is recruiting for a Manager, CMC Regulatory Affairs to be located in Raritan, NJ; Titusville, NJ; or Beerse, Belgium. At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely p

Scientist, Regulatory CMC Dossier - Biotherapeutics

Johnson & Johnson

Spring House, Pennsylvania, USA

Full-time

Description Janssen Research & Development, L.L.C., a division of Johnson & Johnson's Family of Companies, is recruiting for a Scientist, Regulatory CMC Dossier - Biotherapeutics based in Spring House, PA.Remote work options may be considered on a case-by-case basis and if approved by the Company. At the Janssen Pharmaceutical Companies of Johnson & Johnson, we are working to create a world without disease. Transforming lives by finding new and better ways to prevent, intercept, treat and cure

Consultant VI, Duals Regulatory Management

Kaiser Permanente

Oakland, California, USA

Full-time

Description: Remote from any KP location in CA, OR, CO, WA, GA, MD, VA, HI or D.C. Only. ** PLEASE NOTE: Salary ranges are geographically based and the posted range reflects the Northen CA region. Lower salary ranges will apply for other labor markets outside of NCAL Overview: Serves as the accountable lead for duals regulatory submissions required by the Department of Health Care Services (DHCS) and the Department of Managed Health Care (DMHC). Work includes, without limitation, development an

Senior Regulatory Affairs Program Lead

Johnson & Johnson

Irvine, California, USA

Full-time

Description The Cardiovascular & Specialty Solutions (CSS) Group, part of the Medical Tech sector within Johnson & Johnson, is recruiting for a Senior Regulatory Affairs Program Lead for International Registration, as part of the Regulatory Affairs Global Execution team, located in Irvine, CA. At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are sma