*Rate::$40/HR*
*LOCATION:* *Ft. Worth, TX *
*REQ. SKILLS:* *Validation Engineer*
*START DATE: 06/13/2016*
*INTERVIEW: phone screen; Skype*
*DURATION: 7 months +*
Duties:
Support assigned validation activities in a timely manner and in line with
cGMP requirements.
•Author validation protocols and technical reports (e.g., Pre Validation
Studies, Performance Qualifications, Requalifications, Annual Monitoring
Batches).
•Perform process qualification for new equipment and new technologies.
•Contribute to provide experimental data obtained during the validation
activities, which will be used to prepare the related registration
documentation.
Skills:
•Understanding of manufacturing processes and related process equipment.
•Working knowledge of applied statistics, quality systems and regulatory
requirements.
•Experience in executing process validation
•Writing and reviewing protocols and technical reports.
•Fundamental understanding of standard pharmaceutical analytical testing.
Education:
BSc in Chemistry, Microbiology, Pharmacy, Chemical Engineering, or
Pharmaceutical Technology, or equivalent scientific or engineering degree.
Fluent in English and proficient in site local language.
Some lab Experience is a plus.!!
*Thanks & Regards,*
*Kuldeep Yadav {KD}*
*Recruiter - Lead*
*Net**2**Source Inc.*
*kuldeep.ya...@net2source.com <kuldeep.ya...@net2source.com>*
*Gtalk&Yahoo:: kd.intime*
*Direct ::2014792783*
*Tel: (201) 340.8700 x 4**52**|*
*Fax: (201) 221 8131*
*Address: 15 Exchange Place, Suite # 500, Jersey City, NJ - 07302*
*Website:* www.net2source.com
*Microsoft Gold Certified Partner **|** Cisco Certified Premier Partner **|**
Oracle Gold Partner** | **IBM Business Partner** | **ISO 9001:2008
Certified Company** | **NASSCOM Certified Company **| **E-Verified*
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