Hi ,

Hope you are doing great!!

 

We have opening for Validation Analyst

 

*Job Title: Validation Analyst*

*Location: Peapack, NJ *

*Duration: 6+ Months Contract*

 

*JOB DESCRIPTION:*

•         6-8 years of experience in testing domain. 

•         4 to 6 years as validation Analyst 

•         HP ALM hands-on experience 

•         Pharma experience is required 

•         GAMP 5 knowledge 

 

*Technical/Functional Skills  *

•         6 – 8 years of experience in testing domain. 

•         4 to 6 years as Validation Analyst 

•         Documenting functional and integration requirements 

•         Creation (or change of existing) test script documents 

•         Test script updates, configuration changes and related testing 

•         Final Verification testing 

•         Creation of all supporting documentation: technical design, 
installation documents, integration deployment documents, interface mapping 
documents 

•         Strengths should include functional knowledge of various testing 
types & technologies, client interactions, handling teams, project planning 
and co-ordination of team in varied geographies. 

•         Excellent oral and written communication as well as analytical 
and interpersonal skills. 

•         Experience in working with clients from various backgrounds and 
at various geographical locations. 

•         Expertise in QA, Requirement Analysis, Team Management, Planning, 
Estimations, Scheduling, and Defect Management (using ALM-QC). 

•         Should have experience on Test Planning, Testing Effort 
Estimation and Test strategy creation. 

•         Ensure compliance of all testing artifacts and processes 

•         Coordination with stakeholders, BA, testing team and Quality 
team. 

•         Provide status to program team on testing activities of on-going 
applications 

•         Reviews and root cause analysis of testing activities. 

•         Experience within a delivery role 

•         Experience with client facing consulting engagements. 

•         Knowledge of Pharma domain. 

•         Working knowledge of performance testing and tools 

•         HP Quality Center /ALM; MS Dynamics 

•         Should be well versed with the Pharma domain – terminology & 
industry standards. 

•         Should have knowledge of 21 CFR Part 11– Computer Systems 
Validation and other compliance processes.

 

 

*Thanks & Regards,*

*Vamshi*

*Email: **vamsh...@itechus.net* <vamsh...@itechus.net> 

*Direct: 802-227-0236 / Main: 802 383 1500 Ext. 205*

 

 

-- 
You received this message because you are subscribed to the Google Groups 
"CorptoCorp" group.
To unsubscribe from this group and stop receiving emails from it, send an email 
to corptocorp+unsubscr...@googlegroups.com.
To post to this group, send email to corptocorp@googlegroups.com.
Visit this group at https://groups.google.com/group/corptocorp.
For more options, visit https://groups.google.com/d/optout.

Reply via email to