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Resumes 31 - 40 of 977 |
Edison, NJ
... Evaluates validation activities and documentation to ensure that they meet FDA standards, User Requirements, deliverables such as Validation Plan, Test Plan Protocols, Validation Summery report, Risk Assessments Reports, Experience in generating, ...
- Feb 22
Edison, NJ
... Evaluates validation activities and documentation to ensure that they meet FDA standards, User Requirements, deliverables such as Validation Plan, Test Plan Protocols, Validation Summery report, Risk Assessments Reports, Experience in generating, ...
- Feb 21
Edison, NJ
... Clinical Quality Program Standards Drug Utilization Review Medication Therapy Management Medicare and Medicaid Processes FDA Drug Safety Guidelines and SOP for operations Soft Skills: Detail-oriented, time management, collaborative, teamwork, ...
- Feb 19
Bridgewater, NJ
JEAN HALLORAN 908-***-**** (Cell) ad3q98@r.postjobfree.com PROFESSIONAL SUMMARY Experienced and dedicated Regulatory Professional with over sixteen years of Regulatory experience in the pharmaceutical industry with a strong focus on FDA Submissions. ...
- Feb 19
Edison, NJ
... Compliance – Ensured compliance with all CCT standards, SOX, FDA, GXP, CSV, 21 CFR part 11, SDLC, SOP and other regulatory requirements. Celgene Inc. – Summit, NJ (http://www.celgene.com) IT Consultant February 2005 – April 2006 IT Projects – ...
- Feb 17
Princeton, NJ
... Created multiple Oracle instances for Argus Safety & Risk management application according FDA regulations. Setup and Configure HA solution using Oracle physical standby database. Recover standby database as and when required. Monitor and ...
- Feb 14
Edison, NJ
... Well versed with regulations related to prescribed products and medical devices and current with the regulatory requirements and expectations including EMA ICH GVP Modules, FDA IND and NDA reporting requirements and global risk management ...
- Feb 09
Rockaway, NJ
... Documented training according to all regulations and standards including FDA 21CFR820 and ISO 13485. Freelance IT Admin, Miami, FL - PC Technician and IT Support (05/2003 - 01/2012) ●Designed and built custom PCs and networking setups based on the ...
- Feb 09
Roselle Park, NJ
... commodities and multiple lines -Upon filling Entry provide release details to LFD (3461 and ACE results) -Advise OGA status, FDA or Agriculture holds or releases -Upload supporting documentation via DIS or ITACS -File CF-7512/IT In-Bond and arrive ...
- Feb 09
Parlin, NJ
... * Reviewed and approved Batch documentations for FDA regulated products. * Document control coordinator for the organization, keeping track of procedures and their lifecycle, issue new procedures and archive old when no longer needed. * Setup ...
- Feb 06