Engages in activities to provide support to the Compliance and Operational Risk teams in order to provide independent compliance and operational risk oversight of Front Line Unit or Control Function performance and any related third party/vendor relationships in alignment with the Global Compliance ...
The qualified individual will be responsible for managing assigned tasks as part of the DEA Compliance Group as they relate to the Drug Enforcement Administration (DEA), the New Jersey Department of Health and the State of New Jersey Controlled Dangerous Substances (CDS), as well as ensure complianc...
Engages in activities to provide independent compliance and operational risk oversight of Front Line Unit or Control Function (FLU/CF) performance and any related third party/vendor relationships in alignment with the Global Compliance - Enterprise Policy, the Operational Risk Management - Enterpris...
Job Summary:As a member of the Regulatory Compliance NERC Team, the Senior NERC Compliance Specialist provides essential support for NRG’s NERC Compliance Program under the direction of the Sr. Director Regulatory Compliance. In addition to supporting the Regulatory Compliance NERC Team, you will be...
Engages in activities to provide support to the Compliance and Operational Risk teams in order to provide independent compliance and operational risk oversight of Global Compliance and Operational Risk performance and any related third party/vendor relationships in alignment with the Global Complian...
The Enrollment or Compliance Representative provides a variety of support to Brokers assisting with all questions they may have. ...
The qualified individual will be responsible for managing assigned tasks as part of the DEA Compliance Group as they relate to the Drug Enforcement Administration (DEA), the New Jersey Department of Health and the State of New Jersey Controlled Dangerous Substances (CDS), as well as ensure complianc...
In addition to supporting the Regulatory Compliance NERC Team, you will be working with our engineering and plant operations personnel, which will involve travel to various power plants, primarily located within the ERCOT region, to assist in the performance of:. Analyze technical data to demonstrat...
The qualified individual will be responsiblefor managing assigned tasks as part of the DEA Compliance Group asthey relate to the Drug Enforcement Administration (DEA) the NewJersey Department of Health and the State of New Jersey ControlledDangerous Substances (CDS) as well as ensure compliance with...
EHS Compliance Specialist - 3rd Shift. Assists in coordinating the PSM Mechanical Integrity audits, Process Hazard Analysis (PHA), Compliance Audits (CA),and Management of Change (MOC) as required to effectively manage covered processes in compliance with all applicable regulations, including, but n...
The Enrollment or Compliance Representative provides a variety of support to Brokers assisting with all questions they may have. ...
The Senior Regulatory and Compliance Specialist candidate must be knowledgeable in global regulations pertaining to the pharmaceutical industry (or regulated industry equivalent) and their impact on manufacturing processes and practices. The ideal candidate must be agile and have well-developed orga...
The Senior Regulatory and Compliance Specialist candidate must be knowledgeable in global regulations pertaining to the pharmaceutical industry (or regulated industry equivalent) and their impact on manufacturing processes and practices. The ideal candidate must be agile and have well-developed orga...
The Senior Regulatory and Compliance Specialist candidate must be knowledgeable in global regulations pertaining to the pharmaceutical industry (or regulated industry equivalent) and their impact on manufacturing processes and practices. The ideal candidate must be agile and have well-developed orga...
Minimum of 3 years of business experience, with 2 years in HCC or a compliance-related area: monitoring, testing, auditing, finance, compliance, regulatory, law, or a related field is required. Experience in Healthcare Compliance transparency reporting or financial data analysis is preferred. Prefer...
Minimum of years of business experience, with years in HCC or a compliance-related area: monitoring, testing, auditing, finance, compliance, regulatory, law, or a related field is required. Experience in Healthcare Compliance transparency reporting or financial data analysis is preferred. Preferred ...
The Senior Regulatory and Compliance Specialist candidate must be knowledgeable in global regulations pertaining to the pharmaceutical industry (or regulated industry equivalent) and their impact on manufacturing processes and practices. The ideal candidate must be agile and have well-developed orga...
The Regulatory Compliance Specialist will contribute to our organization success by ensuring the organization adheres to legal and relevant regulatory requirements by partnering cross-functionally with internal and external partners. In charge of regulatory compliance monitoring, in partnership with...
Catalent Pharma Solutions in Somerset, NJ is hiring a Senior Regulatory and Compliance Specialist for the Compliance Group. The Senior Regulatory and Compliance Specialist candidate must be knowledgeable in global regulations pertaining to the pharmaceutical industry and their impact on manufacturin...
A project manager (PM) is responsible for the scope, schedule, cost, quality and client satisfaction of a project throughout its entire lifecycle, from Initiating through Closing phases. A project managers role is primarily focused around written and verbal communication to all project stakeholders....
As an individual contributor, the function of a Senior Regulatory Affairs Specialist is to combine knowledge of scientific, regulatory, and business issues to enable i-STAT branded products that are developed, manufactured, or distributed by Point of Care to meet required legislation in the US and E...
As an individual contributor, the function of a Senior Regulatory Affairs Specialist is to combine knowledge of scientific, regulatory, and business issues to enable i-STAT branded products that are developed, manufactured, or distributed by Point of Care to meet required legislation in the US and E...
As an individual contributor, the function of a Senior Regulatory Affairs Specialist is to combine knowledge of scientific, regulatory, and business issues to enable i-STAT branded products that are developed, manufactured, or distributed by Client’s Point of Care to meet required legislation ...
Update and develop procedures for the regulatory affairs in supporting changes in the regulatory landscape, including EU MDR. Years Experience: Must have 3-5 years of experiences in Medical Device Regulatory Affairs. Assist the strategy implementation and operations for regulatory affairs activities...
As an individual contributor, the function of a Senior Regulatory Affairs Specialist is to combine knowledge of scientific, regulatory, and business issues to enable i-STAT branded products that are developed, manufactured, or distributed by Client Point of Care to meet required legislation in the U...