Requirement The following requisition has been assigned:
Contract Long Term TITLE: Life Sciences domain expert STATUS: Open JOB CODE: 17365 LOCATION: Edison, NJ, United States # of Openings: 1 Requisition Details: • 12 - 15 years of experience in Life Science Pharma, Medical Device and IT industry • Excellent understanding of Business Processes Quality, Compliance, Drug Safety, Regulatory Affairs, Customer Relationship Management, Document and Training Management for global Life Sciences Pharma Medical Device organizations • Business Process Analysis and Design - Quality, Compliance, Drug Safety, Regulatory Affairs and Risk Management • Medical Devices - Design Controls, Non-conformance Management, Complaints Management, Regulatory Affairs and Audit Program Management • Standards and Regulations ISO 14385, 18308, 14001, 31000, GAMP5, GxP Manufacturing, Laboratory, Clinical, 21 CFR Part 11, QSR FDA, IEC 62304 Please include all of this information when you first submit the resume. Candidate’s full legal name: Candidate’s email address: Candidate’s telephone number/Mobile: Candidate’s Skype ID & Linked in URL: Candidate’s current location: Candidate’s visa status: Candidate’s ability to start: Desired All inclusive Hourly Rate: Please make sure all details relating to education are on the resume (Education and year of completing) *Thanks,* *Sam* *Tel:-732-917-4895 | eFax:- 732-875-0233* *SourceChip, Inc | **www.sourcechip.net* <http://www.sourcechip.net/> -- You received this message because you are subscribed to the Google Groups "SAP Workflow" group. To unsubscribe from this group and stop receiving emails from it, send an email to sap-workflow+unsubscr...@googlegroups.com. To post to this group, send email to sap-workflow@googlegroups.com. Visit this group at https://groups.google.com/group/sap-workflow. For more options, visit https://groups.google.com/d/optout.
