Hello, Hope you are doing great.
Please review the requirement and if you find it matching your profile then send me your updated resume ASAP *Job Title: Regulatory Business Analyst* *Location: Jersey City, NJ* *Duration: 6+ Months* We are looking for the candidate with Life Science domain exp. only (Pharmaceutical company experience) Mandatory Skills: Strong working knowledge on 1) Submission standards in various formats 2) Good documentation practices and requirements for managing regulated records, Part11 and Computer System Validation guidelines and principles 3) IT systems supporting regulatory affairs such as document management, electronic publishing, and submission systems (e.g., SharePoint, Documentum, InSight Publisher, ISI Toolbox, Synchrony Axway) 4) Skilled in basic technologies (e.g., MS Office Applications, Adobe Acrobat, MS Project) Preferred Skills: Excellent working knowledge on Regulatory Submission Applications based on Documentum / SharePoint. Be able to support business operations of regulatory department Roles and Responsibilities Role: Regulatory business system analyst Responsibility: Support regulatory operations business users and IT support for regulatory submissions IT systems Regards Ashish Gupta 1351 McCarthy Boulevard, Suit 116, Milpitas, CA, USA, 95035 *Phone* : 408-418-5779 ex 253 *Yahoo, Hangouts* : ashish.recruiter12 *Email* : ashish.gu...@idctechnologies.com *URL* : WWW.idctechnologies.com <http://www.idctechnologies.com/> -- -- To unsubscribe from this group, send email to cbe-software-engineer-unsubscr...@googlegroups.com For more options, visit this group at http://groups.google.com/group/CBE-Software-Engineer?hl=en --- You received this message because you are subscribed to the Google Groups "CBE Software Engineer" group. To unsubscribe from this group and stop receiving emails from it, send an email to cbe-software-engineer+unsubscr...@googlegroups.com. For more options, visit https://groups.google.com/d/optout.
