Fwd: Urgent Requirement:Validation Analyst ::Warsaw , IN

2017-03-02 Thread Wasim Ahmed
Hi Associate,


We have an Urgent opening .Please see the Job Description Below and let me
know if you have any consultant available.


*Job Title: Validation Analyst *

*Location: Warsaw, IN*

*Duration: 12+ Months*

*Rate: $40/hr. C2C max*



*Need visa copy and photo id for submission*



Role Description

At least 5 years? hands-on experience in Software Validation in the
Pharmaceutical and/or Medical Devices industries.

-Experience in authoring/executing Validation Master Plan , Risk
Assessment/GxP assessment ,VP, URS, TM, IQ,OQ,PQ protocols, Final
Validation Report.Experience in doing the validation of Manufacturing
applications

Experience in reviewing the existing validation and completing the Gap
assessment

Familiarity with validation of manufacturing shop floor applications will
be a plus

Excellent Communication skills is a must

Ensuring that process followed fully comply with regulatory requirements,
company policies and procedures

Actively maintain the Inventory of existing applications , conducting CSV
determination assessment and risk assessment and mentor the team for the
same.

Manage the execution of remediation procedure for the inventoried systems

Ability to work with teams based at onsite and offshore and achieve project
objectives

Experienced and guiding software validation team in creating quality
documents adhering to GAMP5 and 21 CFR 820 requirements

Demonstrated ability to learn new areas and apply Validation principles

Strong Experience in GAMP4/GAMP5 based validation? Experience in validating
systems against 21 CFR Part 11



Thanks & Regards

*Wasim Ahmed*

Phone : 609-853-0818 X 2178


Fax : 609 799 5746
Email: wasim.ah...@nityo.com
www.nityo.com

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Fwd: Urgent Requirement:Validation Analyst ::Warsaw , IN

2017-03-02 Thread Wasim Ahmed
Hi Associate,


We have an Urgent opening .Please see the Job Description Below and let me
know if you have any consultant available.


*Job Title: Validation Analyst *

*Location: Warsaw, IN*

*Duration: 12+ Months*

*Rate: $40/hr. C2C max*



*Need visa copy and photo id for submission*



Role Description

At least 5 years? hands-on experience in Software Validation in the
Pharmaceutical and/or Medical Devices industries.

-Experience in authoring/executing Validation Master Plan , Risk
Assessment/GxP assessment ,VP, URS, TM, IQ,OQ,PQ protocols, Final
Validation Report.Experience in doing the validation of Manufacturing
applications

Experience in reviewing the existing validation and completing the Gap
assessment

Familiarity with validation of manufacturing shop floor applications will
be a plus

Excellent Communication skills is a must

Ensuring that process followed fully comply with regulatory requirements,
company policies and procedures

Actively maintain the Inventory of existing applications , conducting CSV
determination assessment and risk assessment and mentor the team for the
same.

Manage the execution of remediation procedure for the inventoried systems

Ability to work with teams based at onsite and offshore and achieve project
objectives

Experienced and guiding software validation team in creating quality
documents adhering to GAMP5 and 21 CFR 820 requirements

Demonstrated ability to learn new areas and apply Validation principles

Strong Experience in GAMP4/GAMP5 based validation? Experience in validating
systems against 21 CFR Part 11



Thanks & Regards

*Wasim Ahmed*

Phone : 609-853-0818 X 2178


Fax : 609 799 5746
Email: wasim.ah...@nityo.com
www.nityo.com

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