Home

Requirements for Sr. Validation Consultant for the location Boston, MA (onsite) at Boston, Massachusetts, USA
Email: [email protected]
http://bit.ly/4ey8w48
https://jobs.nvoids.com/job_details.jsp?id=307494&uid=

From:

Manpreet Singh,

1 Point System LLC

[email protected]

Reply to:   [email protected]

Hi,                                 

Hope you are doing well...                     

Below is the very urgent requirement please reviews it and let me know your interest in this requirement. Would appreciate if you can also share your updated resume.                     

Title:                                  Sr. Validation Consultant

Location:                          100% onsite Boston, MA

Duration:                          6+ months              

Job Description:

JOB SCOPE:

Looking for a Sr. Validation Consultant to lead in Boston, MA. 5-7 years experience with 3-5 being in media fills.

Responsibilities:

Lead and perform gap analysis of the sites validation program against current industry regulations and develop validation technical policies and procedures (VMP, Master Standard Operating Procedures, Project Plans etc.) to correct gaps as required. The consultant should be more quality and validation heavy - less production

Provide strong technical guidance and strategy for aseptic media fill-finish manufacturing equipment commissioning and qualification activities including but not limited to development of validation strategy, OOS/OOT investigation, process deviation impact, root cause investigation, process change and optimization.

Lead, coordinate and facilitate aseptic media fill and periodic review activities.

Lead, collaborate and address quality standards for GMP equipment and systems.

MUST be able to write and execute protocols, reports, deviations, gap analyses, risk assessments, etc for aseptic/ media fill processing

Write Summary reports for Commissioning, IOQ and PQ qualification documents. MVPs and Periodic Reviews.

Collaborate with cross-functional team and ensure timely completion of project deliverables.

Apply CGMP and CGDP to all areas of work and independently author and manage execution studies for new equipment and utilities

Also Must have:

- Media Fills/Aseptic Processing

- Write and execute protocols

*Most Important Skills Needed: Validation Engineering, Validation Oversight, Aseptic/Fill Finish, Writing Validation Reports

Thanks & Regards

Manpreet Singh

Technical Recruiter | 1Point System LLC  

Office: +1 205-635-0010   www.1pointsys.com  [email protected]

https://www.linkedin.com/in/manpreet-singh-a475301a5/

115 Stone Village Drive  Suite C  Fort Mill, SC  29708

Keywords: information technology Massachusetts South Carolina
http://bit.ly/4ey8w48
https://jobs.nvoids.com/job_details.jsp?id=307494&uid=
[email protected]
View All
09:02 PM 25-Jan-23


To remove this job post send "job_kill 307494" as subject from [email protected] to [email protected]. Do not write anything extra in the subject line as this is a automatic system which will not work otherwise.


Your reply to [email protected] -
To       

Subject   
Message -

Your email id:

Captcha Image:
Captcha Code:


Pages not loading, taking too much time to load, server timeout or unavailable, or any other issues please contact admin at [email protected]


Time Taken: 31

Location: Boston, Massachusetts