Send Resumes to a...@vertigonconsulting.com
Position: Sr. Validation Analyst Location: Hampton, NJ Duration: 2 months (4-8 weeks) Locals or nearby face to face *Background Qualifications:* § BA/BS or equivalent in life sciences, computer science, engineering or compliance. Advanced degree a plus. § 5+ years experience in a regulated environment (pharmaceutical is required, medical device is desirable). § 5+ years in a computer systems validation role. § Project management experience. § Proven computer validation expertise. § Excellent technical writing and presentation skills. § Strong analytical and problem solving skills § Demonstrable knowledge of the pharmaceutical industry and applicable regulations. § Direct experience with key systems: Document Management, Laboratory Systems, Project Management Systems, Clinical Trial Management Systems, Clinical Data Management Systems, Quality Tracking Systems, Regulatory Information Systems, etc. preferred § Knowledge and experience in the maintenance and use of manufacturing systems, especially in a regulated environment. § Knowledge and experience in the maintenance and use of scientific systems, especially in a regulated environment. § Experience in the validation of manufacturing, laboratory and clinical applications as well as quality systems. § Self-motivated with the ability to work independently. Requires minimal supervision to set and achieve goals. § Some travel required. Thanks & Regards Adem Technical Recruiter Vertigon Consulting Phone: 201-786-2670 Fax: 732-398-0506 Email: a...@vertigonconsulting.com -- You received this message because you are subscribed to the Google Groups "it req" group. To unsubscribe from this group and stop receiving emails from it, send an email to it-req+unsubscr...@googlegroups.com. To post to this group, send email to it-req@googlegroups.com. Visit this group at http://groups.google.com/group/it-req. For more options, visit https://groups.google.com/groups/opt_out.
