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Available Regulatory Affairs jobs in New Jersey

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Your Search Term(s): United States » New Jersey » Regulatory Affairs
Job Posting Search Results 01 - 07 of 07

1
Company Job Title Location Posting Date
Aerotek Professional Services  Documentation Specialist New Branchburg, New Jersey 4/27/2016
...experience. 5 to 7 years in the diagnostics or pharmaceutical industry focusing on quality systems procedures, regulatory affairs/compliance, project management, controlled documentation, product labeling, or change control.
Aerotek Professional Services  Documentation Specialist New Branchburg, New Jersey 4/27/2016
...etc. At least 3 years in the diagnostics or pharmaceutical industry focusing on quality systems procedures, regulatory affairs/compliance, project management, controlled documentation, product labeling, or change control.
Aerotek Clinical  Clinical Trial Disclosure Associate New Woodcliff Lake, New Jersey 4/27/2016
...across multiple disciplines within and outside Regulatory Affairs to drive departmental and project objectives...Responsibilities: Reviews of clinical and regulatory documents and regulatory submissions for data accuracy, consistency...
Aerotek Clinical  Labeling Manager New Bridgewater, New Jersey 4/26/2016
...labeling for accuracy and for other regulatory requirements such as NDC codes...child-resistant. - Liaise with Regulatory Affairs members and other cross-functional...process and coordinate with other Regulatory functions for the submission...
Aerotek Clinical  Clinical Trial Disclosure Associate Woodcliff Lake, New Jersey 4/22/2016
...across multiple disciplines within and outside Regulatory Affairs to drive departmental and project objectives...be extended to: - reviews of clinical and regulatory documents and regulatory submissions for data accuracy, consistency...
Aerotek Clinical  Clinical Trial Manager (CTM) - MNKJP00000513 Hampton, New Jersey 2/19/2016
...departments (eg, Medical Science, Regulatory Affairs, Data Management). May participate...with GCP/ICH and any other regulatory requirements and works cooperatively...Knowledge of cGCP, ICH and FDA regulatory requirements. * Solid project...
Aerotek Clinical  Clinical Safety Associate / Case Processing Princeton, New Jersey 1/26/2016
...from Clinical Operations, Regulatory Affairs, Quality and Medical Affairs. Essential Duties and Responsibilities...Processing Mgrs, and Medical Affairs to identify process improvement...Guidelines, ICH Guidelines, Regulatory Approval Process and Drug...

Job Posting Search Results 01 - 07 of 07
1

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