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Regulatory Operations Associate (Documentum, Core Dossier) - (US-NJ-Northern New Jersey)
Compensation: $80K - $90K / Year
Minimum Education: Bachelors
Job Type: Full Time
Jobcode: JV 060109
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Click Here to Apply OnlineOur Client - a leader in the pharmaceutical industry, is currently searching for a Regulatory Operations Associate.
To apply you must have a minimum of 10 years experience working within the pharmaceutical industry and possess knowledge of the Drug Development Process. You must possess extensive experience working with validated systems, understanding of compliance and Part 11, experience in writing procedures, process development, documentation, and have a HIGH level of expertise with Documentum. Experience with the Microsoft Suite of products, CoreDossier and ISIToolbox are a huge plus..
You should have strong project management skills, excellent interpersonal, communication, organizational and follow-up skills and should demonstrate personal initiative, responsibility and leadership and flexibility. In this position you must be able to work under limited supervision and to handle multiple assignments with limited time constraints.
You must have a Bachelor’s degree in Sciences, Business or MIS to be considered.
Major responsibilities will include working with the following:
Document Management Operations
Records Management
Procedural Compliance and Maintenance
Scanning Support
eRoom Administration
Computer System Validation
If you meet the above criteria and want to learn more, please first send your resume to Virginia@BrilliantLeap.com, then call her at (973) 744-8164.
Visit our blog at www.BrilliantLeap.com/blog
Virginia Backaitis
BrilliantLeap!
41 Vreeland Ave
Totowa, NJ 07512
Phone: 973-744-8164
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