regulatory Jobs in charlotte, nc

Refine Results
1 - 15 of 15 Jobs

Regulatory Reporting Analyst

Indsafri

Charlotte, North Carolina, USA

Contract

Job Description: Title: Regulatory Reporting Data Analyst Location: Charlotte NC- onsite 3 days per week preferred, open to other locations: Chandler AZ, Addison TX, Minneapolis MN, Summit NJ, San Francisco CA or Des Moines IA Contract Duration: Through 1/2/2025 The selected candidate will require to Y14Q Sch H regulatory reports instructions , map reporting requirements to physical elements in CBL system and manage the defects aligned to CBL domain through the entire lifecycle of defect manag

Regulatory Reporting Operations Senior Professional

Bank Of America

Charlotte, North Carolina, USA

Full-time

At Bank of America, we are guided by a common purpose to help make financial lives better through the power of every connection. Responsible Growth is how we run our company and how we deliver for our clients, teammates, communities and shareholders every day. One of the keys to driving Responsible Growth is being a great place to work for our teammates around the world. We're devoted to being a diverse and inclusive workplace for everyone. We hire individuals with a broad range of backgrounds

Regulatory Reporting and Axiom SL Specialist

Lorven Technologies, Inc.

Charlotte, North Carolina, USA

Full-time, Third Party, Contract

Job Title: Regulatory Reporting and AxiomSL Specialist Location: Charlotte, NC (Preferred), New Jersey, Chandler AZ, Minneapolis MN, Des Moines IA, Saint Luis, Denver CO Hybrid, a consultant needs to be in the office for 3 days a week" Job Description: Regulatory Reporting Expertise: Extensive experience in installation, administration, development, and configuration of US regulatory reports such as FR Y-9C, FR Y-14 A/Q/M, FFIEC031/041, FFIEC009, FRY-15, FRY-11/2314, liquidity reporting, Base

Regulatory Reporting Consultant

Shimento, Inc.

Charlotte, North Carolina, USA

Contract, Third Party

Financial Regulatory Reporting Consultant Location:- Dallas, TX, NJ, Phoenix AZ, South Carolina, Minneapolis, MN, Concord, CA, San Francisco, CA, 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-14M,

Business Execution Consultant 5 - Contingent Regulatory Reporting QA Transactional Test

Pinnacle Group

Charlotte, North Carolina, USA

Full-time

Title: Software QA Engineer Duration: 12 Months (Possible extension) Location: Charlotte, NC (Hybrid) W2 Candidates only Description: Consult as an expert to develop or influence initiatives and resources for highly complex business and technical needs across Business Execution. Consult on the strategy and resolution of highly complex and unique challenges requiring in-depth evaluation across multiple areas, delivering solutions that are long-term, large-scale and require vision, creativity,

Global Regulatory Strategist

Softpath System, LLC.

Remote

Third Party, Contract

Hi, Hope you are doing great.! My name is Rekha and I am a Staffing Specialist at Softpath System LLC. I am reaching out to you on an exciting job opportunity with one of our clients. Position: Global Regulatory Strategist Location: Remote Type: Contract JOB DESCRIPTION Liaison between Country Regulatory Managers and Global Regulatory Teams/Development Teams/Brand Teams/Operating Committees Responsible in partnership with local GRS for generating, implementing and executing regulatory strategy

Regulatory Affairs Specialist

AR Val Services

Remote

Contract

Responsible for the global coordination and the preparation of documents/packages for regulatory submissions. In this position you will also review and evaluate technical and scientific data and reports required for submission . Essential Duties and Responsibilities Supports regulatory project plan execution Maintain awareness of regulatory requirements and ensure continued learning Maintain regulatory files in a format consistent with requirements Participate as an active team member of projec

CMC 2 Regulatory affairs

Softpath System, LLC.

Remote or Rahway, New Jersey, USA

Contract, Third Party

Hi, Hope you are doing great.! My name is Rekha and I am a Staffing Specialist at Softpath System LLC. I am reaching out to you on an exciting job opportunity with one of our clients. Title: CMC 2 Regulatory affairs Location: Rahway, NJ - Onsite Type: Contract Responsibilities: Well versed in performing CMC compliance activities including Gap Analysis; assessment for Annex 3 comparative table with reference EU Member States Manage execution / authoring and review of CMC documentation (Module 1

CMC Regulatory Senior Manager

Digitive LLC

Remote

Contract

Regulatory & Medical Affairs - Regulatory Studio - CMC Senior Manager Location: RemoteVertical- Life sciences Contract Job Description: PREREQUISITES BS/BA degree in Scientific Discipline (Masters or higher preferred) with 5+ years in the pharmaceutical industry, preferably with 3+ years CMC regulatory experience, Sterile Injectable experience preferred. Responsibilities will include, but are not limited to, the following: 1. Participate in the development of the CMC regulatory strategy for

Global Regulatory Strategist

Softpath System, LLC.

Remote

Third Party, Contract

Title: Global Regulatory Strategist Location: Remote Type: Contract Job Description: Position Summary / Objective Liaison between Country Regulatory Managers and Global Regulatory Teams/Development Teams/Brand Teams/Operating CommitteesResponsible in partnership with local GRS for generating, implementing and executing regulatory strategy and submission plans for development and life cycle products for the regionProvides regional input into Global Regulatory Plan and Global Submission PlanProvid

CMC Regulatory Affairs Manager

TechSpace Solutions Inc.

Remote

Third Party, Contract

Job Title : CMC Regulatory Affairs Manager Location :Remote Duration : 12 Months Job Description: Well versed in performing CMC compliance activities including Gap Analysis, CMC comparison and validation for the quality reportsExperienced in authoring of assessment reports and Part2/ Expert reports for DossiersExperience in reviewing of quality documents such as Reformulation studies, process validations, particle size method implementation and specification, stability indicating methods implem

Global Regulatory Strategist@Remote

HUMAC INC.

Remote

Contract

Global Regulatory Strategist Location: Remote JOB DESCRIPTION Position Summary / Objective Liaison between Country Regulatory Managers and Global Regulatory Teams/Development Teams/Brand Teams/Operating Committees Responsible in partnership with local GRS for generating, implementing and executing regulatory strategy and submission plans for development and life cycle products for the region Provides regional input into Global Regulatory Plan and Global Submission Plan Provides information and p

Principal Regulatory Affairs Specialist (remote)

Medtronic

Remote or Los Angeles, California, USA

Full-time

Careers that Change Lives Together, we can change healthcare worldwide. At Medtronic, we push the limits of what technology, therapies and services can do to help alleviate pain, restore health, and extend life. We challenge ourselves and each other to make tomorrow better than yesterday. It is what makes this an exciting and rewarding place to be. We want to accelerate and advance our ability to create meaningful innovations - but we will only succeed with the right people on our team. Let's w

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.

Principal Regulatory Affairs Specialist (Remote)

Medtronic

Remote or Los Angeles, California, USA

Full-time

Careers that Change Lives Together, we can change healthcare worldwide. At Medtronic, we push the limits of what technology, therapies and services can do to help alleviate pain, restore health, and extend life. We challenge ourselves and each other to make tomorrow better than yesterday. It is what makes this an exciting and rewarding place to be. We want to accelerate and advance our ability to create meaningful innovations - but we will only succeed with the right people on our team. Let's w