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FDA LIMS JSON HL7 XML XSLT Analyst
(Jobs in Taylorsville, UT)
 
Requirement id 118053
Job title Analyst
Job location in Taylorsville, UT
Skills required FDA, LIMS, Crystal Report Writing, JSON HL7 XML XSLT
Open Date 21-Jul-2021
Close Date
Job type Contract
Duration 12 Months
Compensation DOE
Status requirement ---
Job interview type ---
   Email Recruiter: coolsoft
Job Description Analyst: FDA, LIMS, Crystal Report Writing, JSON HL7 XML XSLT

start date:3/1/2021

End date:07/29/2022

submission deadline:7/26/2021 10:00:00 PM

client info : DOH

Note:

* Please ensure that the candidate is local or interested in relocating to Salt Lake. This will be an onsite role.

* Any person with the legal right to work in the US may be considered. However, the State of Utah will not sponsor any candidate. Vendor will be responsible for any requirements to legally work in the US.

* Vendors have a maximum of 3 bids. Once you use a bid, it cannot be credited.


Description:

• Support new LIMS (Labware v. 8) rollouts.

• Provide ongoing LIMS support.

• Maintain working knowledge of LIMS.

• Work with business analyst team to support communication with UPHL Leadership on LIMS priorities, data security, and informatics needs.

• Troubleshoot system functionality and make recommendations on solutions in a timely manner.

• Identify measures or indicators of system performance and the actions needed to improve or correct performance, relative to the goals of the system.

• Consider the relative costs and benefits of potential actions to choose the most appropriate one.


The Ideal Candidate has:

• Experience implementing and maintaining complex software systems.

• The ability to determine user needs and convert to business and technical requirements.

• The ability to evaluate and test software functionality to meet a business need.

• The capacity to simultaneously handle multiple projects or tasks.

• Experience teaching end users how to use complex software systems.

• The knowledge of flow diagram software and the ability to create a workflow.

• The capability to organize and write documentation that clearly states and outlines the objectives.

• The capacity to see the forest for the trees and translate the concepts to the testing personnel and leadership bi-directional.

• The ability to derive joy from diving directly into complex challenges and deliver solutions.

• Experience working with large databases along with data retrieval.

• An understanding of general laboratory processes, terminologies, quality, and regulatory requirements.

• Experience of performing complex SQL queries, modifying minor coding issues and building customized report settings in Crystal Reports.

Preference may be given to applicants with:

• Experience working with and supporting other laboratory information management systems Labware LIMS.

• A knowledge and understanding of the following listed in each section:

• Environmental Chemistry Section: Sample preparation batch vs. analysis batch; detection limits vs. reporting limits; standards vs reagents; instrument blank vs. reagent blank vs. field blank, TNI/EPA reporting regulations.

• Infectious Disease/Toxicology Sections: Chain of Custody; understanding reagent batches vs cultures, overall reportable results determined by an algorithm of test results. Building reflex rules based on test results. CLIA/FDA/CDC reporting elements.
 
Call 502-379-4456 Ext 100 for more details. Please provide Requirement id: 118053 while calling.
 
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Note:

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(Analyst: FDA, LIMS, Crystal Report Writing, JSON HL7 XML XSLT in Taylorsville, UT)
     
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