Compliance Program Specialist Jobs in Bridgewater

Job Information Bristol Myers Squibb Clinical Trial Result Specialist in Princeton New Jersey Bristol-Myers Squibb is a global Biopharma company committed to a single mission: to discover, develop, and deliver innovative ..

Bristol-Myers Squibb is a global Biopharma company committed to a single mission: to discover, develop, and deliver innovative medicines focused on helping millions of patients around the world in disease areas ..

... BMS’ medical product data management program Establishes and maintains a set ... guidances with impact to BMS compliance and processes, especially where systems ... Summary / Objective The Regulatory..

Position Summary:The International Trade Compliance Coordinator will provide strategic leadership ... programs, including PVH Duty Drawback program. The individual is responsible for ... requests, entry corrections, manage key compliance indicators,..

Position Summary:The International Trade Compliance Coordinator will provide strategic leadership ... programs, including PVH Duty Drawback program. The individual is responsible for ... requests, entry corrections, manage key compliance indicators,..

... and make a difference. The Compliance Supervisor is responsible for overseeing ... adhere to the Site Training Program and trains other staff members. ... will also assist the Sr...

... is currently looking for Export Compliance Specialist in New Brunswick, NJ with ... top clients. Job Title: Export Compliance Specialist Job Id : 23-03895 Location ... Fri, Business Hours..

... or exported goods ensuring customs compliance in all areasEnsure compliant processing ... directly with CBP regarding any compliance concerns/issues/new programs.Monitor responsibilities of internal ... information to PVH,industry:Retail,title:Director International Trade..

Job Information Bristol Myers Squibb Compliance Systems Specialist in New Brunswick New Jersey ... make a difference. Summary: The Compliance Systems Specialist (CSS) is accountable for the ... of the..

... preclinical research processes to determine compliance with regulatory requirements, guidelines and ... act as a quality and compliance subject matter expert (SME) to ... external contract laboratories to assess..