Fwd: NEED USC AND GC : Mechanical Engineer_Validation Engineer (Medical device) Specialist -Warsaw,IN

2017-01-24 Thread vicky menon
*Vicky Kumar *

*IT–SCIENT LLC, Fremont, CA, USA ll Phone USA : (510) 516-7899 ​EMAIL: *
*vi...@itscient.com* 

-- Forwarded message --
From: vicky menon 
Date: Mon, Jan 23, 2017 at 9:02 PM
Subject: NEED USC AND GC : Mechanical Engineer_Validation Engineer (Medical
device) Specialist -Warsaw,IN
To: chitranja...@itscient.com, vi...@itscient.com



*Hi Folks,*

*Hope you're doing great there..!*

*Please find the requirement given below .Share your profile and details to
the given address.*



*ITS AN FULL TIME PERMANENT JOB OPPORTUNITY* *.*



*Role :-  Mechanical Engineer/Validation Engineer (Medical device)*

*Location:  Warsaw,IN*

*Duration : FTE*

*Client :TCS/Zimmer*

*Salary : $65k*

*Note :-  PLEASE AVOID DOUBLE SUBMISSION !! *

* Job Description:*

Skills :- Medical Devices, Process Validation, IQ/OQ/PQ, 21 CFR Part 11,
Statistical Analysis Tools, Inspection Techniques, SPC

*Relevant Experience*

*(in Yrs)*

1-3 years

*Technical/Functional Skills*

ü  Knowledge of basic quality tools, risk analysis, statistics (SPC)

ü  Ability to read and understand engineering drawings

ü  Knowledge of Quality System requirements, ISO and FDA requirements
(preferred)

ü  Ability to effectively work within a team to expedite completion of
critical project tasks with other functional groups

ü  Experience with Statistical Process Control and inspection techniques

*Experience Required*

1-3 years

*Roles & Responsibilities*

ü  Interface with Manufacturing/Process Engineering, R&D, and Regulatory
departments to resolve process issues and implement changes.

ü  Apply knowledge of process control tools, statistical sampling, and
other analytical techniques to maximize the quality and flow of product
through the production line.

ü  Identify, analyze, and manage risk through product life cycle with use
of FMEA and other risk management tools.



*SKILL SETS SUMMARY* *:-*

* Full Name*



*Contact Number*



*Email ID*



*Current location*



*Salary*



*Relocation Yes /No*



*Work Authorization in USA*



*Total Years of Exp*



*Skype ID*



*LinkedIn Id*



*Any Interview In Pipeline ?*



*Any Offer In Pipeline?*



*Availability for Phone Interview & Skype*



*2 TIME SLOTS FOR INTERVIEW*

*//*

*Start Date*



 Chitranjan Kumar Singh

IT–SCIENT LLC, Fremont, CA, USA ll Phone USA : (510) 516-7833 ​EMAIL:
chitranja...@itscient.com

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NEED USC AND GC : Mechanical Engineer_Validation Engineer (Medical device) Specialist -Warsaw,IN

2017-01-19 Thread vicky menon
*Hi Folks,*

*Hope you're doing great there..!*

*Please find the requirement given below .Share your profile and details to
the given address.*



*ITS AN FULL TIME PERMANENT JOB OPPORTUNITY* *.*



*Role :-  Mechanical Engineer/Validation Engineer (Medical device)*

*Location:  Warsaw,IN*

*Duration : FTE*

*Client :TCS/Zimmer*

*Salary : $65k*



*Note :-  PLEASE AVOID DOUBLE SUBMISSION !!  Job Description:*

Skills :- Medical Devices, Process Validation, IQ/OQ/PQ, 21 CFR Part 11,
Statistical Analysis Tools, Inspection Techniques, SPC

*Relevant Experience*

*(in Yrs)*

1-3 years

*Technical/Functional Skills*

ü  Knowledge of basic quality tools, risk analysis, statistics (SPC)

ü  Ability to read and understand engineering drawings

ü  Knowledge of Quality System requirements, ISO and FDA requirements
(preferred)

ü  Ability to effectively work within a team to expedite completion of
critical project tasks with other functional groups

ü  Experience with Statistical Process Control and inspection techniques

*Experience Required*

1-3 years

*Roles & Responsibilities*

ü  Interface with Manufacturing/Process Engineering, R&D, and Regulatory
departments to resolve process issues and implement changes.

ü  Apply knowledge of process control tools, statistical sampling, and
other analytical techniques to maximize the quality and flow of product
through the production line.

ü  Identify, analyze, and manage risk through product life cycle with use
of FMEA and other risk management tools.



*SKILL SETS SUMMARY* *:-*

* Full Name*



*Contact Number*



*Email ID*



*Current location*



*Salary*



*Relocation Yes /No*



*Work Authorization in USA*



*Total Years of Exp*



*Skype ID*



*LinkedIn Id*



*Any Interview In Pipeline ?*



*Any Offer In Pipeline?*



*Availability for Phone Interview & Skype*



*2 TIME SLOTS FOR INTERVIEW*

*//*

*Start Date*





*Chitranjan Kumar Singh*



*IT–SCIENT LLC, Fremont, CA, USA ll Phone USA : (510) 516-7833*

 *​**EMAIL: **chiitranjan.s**@itscient.com* 

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NEED USC AND GC : Mechanical Engineer_Validation Engineer (Medical device) Specialist -Warsaw,IN

2017-01-18 Thread vicky menon
*Hi Folks,*

*Hope you're doing great there..!*

*Please find the requirement given below .Share your profile and details to
the given address.*

*ITS AN FULL TIME PERMANENT JOB* *OPPORTUNITY* *.*



*Role :-  Mechanical Engineer/Validation Engineer (Medical device)*

*Location:  **Warsaw,IN*

*Duration : FTE*

*Client :TCS/Zimmer*

*Salary : $65k*



*Note :-  PLEASE AVOID DOUBLE SUBMISSION !! Job Description:*

Skills :- Medical Devices, Process Validation, IQ/OQ/PQ, 21 CFR Part 11,
Statistical Analysis Tools, Inspection Techniques, SPC

*Relevant Experience*

*(in Yrs)*

1-3 years

*Technical/Functional Skills*

ü  Knowledge of basic quality tools, risk analysis, statistics (SPC)

ü  Ability to read and understand engineering drawings

ü  Knowledge of Quality System requirements, ISO and FDA requirements
(preferred)

ü  Ability to effectively work within a team to expedite completion of
critical project tasks with other functional groups

ü  Experience with Statistical Process Control and inspection techniques

*Experience Required*

1-3 years

*Roles & Responsibilities*

ü  Interface with Manufacturing/Process Engineering, R&D, and Regulatory
departments to resolve process issues and implement changes.

ü  Apply knowledge of process control tools, statistical sampling, and
other analytical techniques to maximize the quality and flow of product
through the production line.

ü  Identify, analyze, and manage risk through product life cycle with use
of FMEA and other risk management tools.



*SKILL SETS SUMMARY* *:-*

* Full Name*



*Contact Number*



*Email ID*



*Current location*



*Salary*



*Relocation Yes /No*



*Work Authorization in USA*



*Total Years of Exp*



*Skype ID*



*LinkedIn Id*



*Any Interview In Pipeline ?*



*Any Offer In Pipeline?*



*Availability for Phone Interview & Skype*



*2 TIME SLOTS FOR INTERVIEW*

*//*

*Start Date*




*Chitranjan Kumar Singh*

*IT–SCIENT LLC, Fremont, CA, USA ll Phone USA : (510) 516-7833*
* ​EMAIL: chiitranjan.s**@itscient.com* 

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NEED USC AND GC : Mechanical Engineer_Validation Engineer (Medical device) Specialist -Warsaw,IN

2017-01-17 Thread vicky menon
*Hi Folks,*

*Hope you're doing great there..!*

*Please find the requirement given below .Share your profile and details to
the given address.*

*Please respond back to :-   * *vi...@itscient.com  *



*ITS AN FULL TIME PERMANENT JOB* *OPPORTUNITY* *.*



*Role :-  Mechanical Engineer/Validation Engineer (Medical device)*

*Location:  **Warsaw,IN*

*Duration : FTE*

*Client :TCS/Zimmer*

*Salary : $65k*



*Note :-  PLEASE AVOID DOUBLE SUBMISSION !! Job Description:*

Skills :- Medical Devices, Process Validation, IQ/OQ/PQ, 21 CFR Part 11,
Statistical Analysis Tools, Inspection Techniques, SPC

*Relevant Experience*

*(in Yrs)*

1-3 years

*Technical/Functional Skills*

ü  Knowledge of basic quality tools, risk analysis, statistics (SPC)

ü  Ability to read and understand engineering drawings

ü  Knowledge of Quality System requirements, ISO and FDA requirements
(preferred)

ü  Ability to effectively work within a team to expedite completion of
critical project tasks with other functional groups

ü  Experience with Statistical Process Control and inspection techniques

*Experience Required*

1-3 years

*Roles & Responsibilities*

ü  Interface with Manufacturing/Process Engineering, R&D, and Regulatory
departments to resolve process issues and implement changes.

ü  Apply knowledge of process control tools, statistical sampling, and
other analytical techniques to maximize the quality and flow of product
through the production line.

ü  Identify, analyze, and manage risk through product life cycle with use
of FMEA and other risk management tools.



*SKILL SETS SUMMARY* *:-*

* Full Name*



*Contact Number*



*Email ID*



*Current location*



*Salary*



*Relocation Yes /No*



*Work Authorization in USA*



*Total Years of Exp*



*Skype ID*



*LinkedIn Id*



*Any Interview In Pipeline ?*



*Any Offer In Pipeline?*



*Availability for Phone Interview & Skype*



*2 TIME SLOTS FOR INTERVIEW*

*//*

*Start Date*




*Chitranjan Kumar Singh*

*IT–SCIENT LLC, Fremont, CA, USA ll Phone USA : (510) 516-7833*
* ​EMAIL: chiitranjan.s**@itscient.com* 

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NEED USC AND GC : Mechanical Engineer_Validation Engineer (Medical device) Specialist -Warsaw,IN

2017-01-16 Thread vicky menon
*Hi Folks,*

*Hope you're doing great there..!*

*Please find the requirement given below .Share your profile and details to
the given address.*

*Please respond back to :-   * *vi...@itscient.com  *



*ITS AN FULL TIME PERMANENT JOB* *OPPORTUNITY* *.*



*Role :-  Mechanical Engineer/Validation Engineer (Medical device)*

*Location:  **Warsaw,IN*

*Duration : FTE*

*Client :TCS/Zimmer*

*Salary : $65k*



*Note :-  PLEASE AVOID DOUBLE SUBMISSION !! Job Description:*

Skills :- Medical Devices, Process Validation, IQ/OQ/PQ, 21 CFR Part 11,
Statistical Analysis Tools, Inspection Techniques, SPC

*Relevant Experience*

*(in Yrs)*

1-3 years

*Technical/Functional Skills*

ü  Knowledge of basic quality tools, risk analysis, statistics (SPC)

ü  Ability to read and understand engineering drawings

ü  Knowledge of Quality System requirements, ISO and FDA requirements
(preferred)

ü  Ability to effectively work within a team to expedite completion of
critical project tasks with other functional groups

ü  Experience with Statistical Process Control and inspection techniques

*Experience Required*

1-3 years

*Roles & Responsibilities*

ü  Interface with Manufacturing/Process Engineering, R&D, and Regulatory
departments to resolve process issues and implement changes.

ü  Apply knowledge of process control tools, statistical sampling, and
other analytical techniques to maximize the quality and flow of product
through the production line.

ü  Identify, analyze, and manage risk through product life cycle with use
of FMEA and other risk management tools.



*SKILL SETS SUMMARY* *:-*

* Full Name*



*Contact Number*



*Email ID*



*Current location*



*Salary*



*Relocation Yes /No*



*Work Authorization in USA*



*Total Years of Exp*



*Skype ID*



*LinkedIn Id*



*Any Interview In Pipeline ?*



*Any Offer In Pipeline?*



*Availability for Phone Interview & Skype*



*2 TIME SLOTS FOR INTERVIEW*

*//*

*Start Date*





*Vicky Kumar *

*IT–SCIENT LLC, Fremont, CA, USA ll Phone USA : (510) 516-7899 ​EMAIL: *
*vi...@itscient.com* 

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