*Hello *

*This is Dinesh from Saxon Global. Please go through the job description
below for a **Senior Validation Analyst Consultant (QA). **If you are
interested, please reply my email with an updated copy of your resume or
reach me at 972 550 9346 X 203.*

If you have any profiles please forward them to *din...@saxonglobal.com

*Job Title: Senior Validation Analyst Consultant (QA)*

*Location: St Louis, MO*

*Duration: 6-12 Months *

Job Description:

Required Skills:

·         Essential:  5+ years LIMS Validation Analyst / QA work

·         Essential: 5+ years  Pharmaceutical Industry experience


·         Support Labvantage LIMS project.

*Activities and Responsibilities:*

• Analyze LIMS Business/User Requirement Specifications

• Analyze OQ/MQ/PQ testing needs

• Coordinate scheduling of validation testing with key site staff (site
admins/site QA)

• Develop OQ/MQ and, if necessary, PQ plans and test cases

• Execute OQ/MQ/PQ plans and test cases

• Identify deviations

• Track LIMS validation activities and test results

• Prepare detailed reports and design documents based on results

• Resolve minor testing problems

*Experience / Skills Needed: *

1) Must have experience with writing FDA Validation documents.

2) Experience writing detailed software testing plans needed.

3) Previous experience working with team on software implementations

4) Knowledge of pharmaceutical laboratory testing using LABVANTAGE LIMS

5) 5+ years working in Quality area with software testing needed.

Education Required: Training in quality related field required.


Best Regards,


Sr. IT Recruiter

Desk: 972 550 9346 ext 203

E-mail : *din...@saxonglobal.com <din...@saxonglobal.com>*

G-talk : dineshrecruite...@gmail.com


*1320 Greenway Drive, Suite 660 Irving, TX-75038*


*“ Even At Your Best Someone will always have something **Negative** to
Say, Pursue Greatness Anyway..”*

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