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 |
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| DeegitTM Inc | Technology Consulting |
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| 1900 E Golf Rd., Suite 925 | Schaumburg, IL 60173 |
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| Phone: (847) 440 2436 Ext. 392 |
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| Email: nanda@deegit.com |
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