Hello,

Sunrise Systems Inc is an IT staff augmentation company and a direct 
vendor for various fortune 1000 clients. Kindly go through the following 
requirements and send me your resume in word format.
Please include your Candidate's complete name, location, availability, 
rate and contact  information in the body of the email along with word 
copy of the resume.

Please keep the subject line while responding to this email. If you have 
any more questions, feel free to give me a call.
Thanks!

--
Sincerely,
Dave Karlekar
Sunrise Systems
[EMAIL PROTECTED]
www.sunrisesys.com
732-603-2200 X-216
732-603-2208 (Fax)
-------------------------------------
Job id - PZ30871QACA
Client - Pharma Company
Title - Quauality Compliance Analyst - with Pharma Domain Experience
Location - La Jolla, CA
Duration - 6 Months
Rate - Open

Quauality Compliance Analyst (regulatory, legal, corporate policy) working in 
Pharmaceutical Domain

Description:
Provide support for departmental record management in compliance with corporate 
and divisional policy and requirements.
Create, maintain, manage and/or coordinate the storage/archive of the internal 
records and e-signature processes.
Contribute to the process implementations planning and post implementation of 
monitorings and feedback
Using technological tool (e.g. SharePoint), assist in bringing awareness and 
communications of quality and compliance practice.
Assist in internal and external audit preparations, organizations and readiness.
Assist in conducting internal project compliance review and identifying area of 
continuous improvement.
Apply quality concept and tool sets, create quality metrics and measures.

Note - the context of compliance includes regulatory, legal, corporate policy.

Qualifications:
Prior working experience in Quality and Compliance organization in 
Pharmaceutical industry.
Prior working experience in record management process.
Be very familiar with software development lifecycle and Information Technology 
processes.
Previous working experiences in using quality planning, analysis and metrics 
tools (such as root cause, affinity, HOQ, SIPOC, Fishbone, etc.)

Highly Proficient in using software tools such as MS Office, Visio, 
Documentation management system (Documentum, SharePoint), etc.
Working knowledge in regulations including GXPs and Part 11.
Effective written communication as well as verbal communications. Experience as 
a technical writer is a plus.






--~--~---------~--~----~------------~-------~--~----~
You received this message because you are subscribed to the Google Groups 
"Embedded_C++_VC++" group.
To post to this group, send email to [email protected]
To unsubscribe from this group, send email to [EMAIL PROTECTED]
For more options, visit this group at 
http://groups.google.co.in/group/Embedded_C_VC?hl=en
-~----------~----~----~----~------~----~------~--~---

Reply via email to