Performs the calibration and validation of test and data analysis equipment and systems used for clinical research, trials and product testing. Assists in equipment selection, specification and negotiation of competitive pricing. Maintains all documentation pertaining to qualification and validation. May develop procedures and/or protocols. Also serves as information resource for validation technicians, contractors and vendors. This role is intended for use by companies in the Life Sciences and Medical Device industries and should be used for those individuals validating results for clinical research, clinical trials and manufacturing testing.
The CSV will document and validate the deployment of Windows 10 upgrades and document changes respectively. Candidate will write, edit, route and approve appropriate documentation associated with each system upgrade and good documentation skills are a must. Candidate will need to be able to execute test protocols as needed for each upgrade. Candidate will need to be able to work on multiple projects at the same time and manage priorities. Working independently is a must. The Analyst will provide project management updates to both customer and PE management, and must be willing to travel to customer site.
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