Hi,

Hope you are doing good!!



Please go through the below requirement and let me know your interest ASAP.



*Title : Quality Engineer*

*Location : Fridley, MN*

*Duration : 6+ months*



*Hiring only USC, GC’s and GC EAD*



*Skill set: *

1)  experience in Validation areas (Medical Device or other regulated
Industry)

2) Experience with Site Validation Master Plan Activities



Job Description:



*Validation Master Plan (VMP) Analyst *

Perform assigned duties under the guidance of the SVMP Program Owner.
Primary duties include:

• Participate in the creation/ maintenance of SVMP inventories.

• Review the SVMP inventories with corresponding owner.

• Monitor the Site Validation Master Plan Activities to assure that they
are completed on time; inform in advance when conflicting issues appear
that could impact the proposed completion date.

• Create and publish reports about the status of the Validation Master Plan
activities.

• Compile and report on established validation metrics.

• Perform Validation Periodic Assessments to determine the maintenance of
the validated state.



*QUALIFICATIONS *

*Education: *

• 4-year Engineering or Science degree preferred

*Experience: *

• 5+ years of experience in Validation areas (Medical Device or other
regulated Industry) with a Bachelor’s Degree or above



*Skills: *

• Strong organization skills

• Proficient with Microsoft Word and Excel

• Excellent Verbal and written communication skills

-- 

Kind regards,

Nanda Kishore | Technical Recruiter



<https://www.facebook.com/DeegitInc/>





*DeegitTM Inc* | Technology Consulting



1900 E Golf Rd., Suite 925 | Schaumburg, IL 60173



*Phone*: (847) 440 2436 Ext. 392



Email: na...@deegit.com



Skype:nanda.neoarden...@gmail.com

www.deegit.com

<https://www.linkedin.com/company/deegit-inc>

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