QA Executive - Bioanalytical - Vimta Labs Ltd

Hyderabad
Full-Time
Junior: 1 to 3 years
1L - 3.5L (Per Year)
Posted on Nov 12 2024

About the Job

Skills

"Internal Quality Audits"
In-process
QMS Requirements
GXP's
"Protocol review"
"method validation protocols"
Final STP's
"calibration data"

QA Executive - Bioanalytical - Vimta Labs Ltd


Exp: 1-3 years


CTC: As per market standards.


Location: Cherlapally, Hyderabad.


Primary Responsibilities:

 

  1. Conduct In-process and study audits of Bioanalytical Department to verify the systems, process comply to QMS requirements, applicable guidelines and GXP's, Regulatory and Sponsor’s requirements. Communicate the findings of the audits to the auditees, Reporting manager and Quality Manager.
  2. Review of protocols, Method Validation protocols, Method Validation Reports, Final STPs, SOPs, Calibration data Concentration and statistical data.
  3. Perform Internal Quality Audits (IQA) of bioanalytical and other cross functional departments as directed by the Quality Manager. 
  4. Ensure that the requisite corrective and preventive actions are taken and implemented. 
  5. Review of Calibration data.

 

  Secondary Responsibilities:

 

  1. Issuance of SOPs, forms and other documents and maintaining track of the issued documents, archival of documents as and when required.


Interested candidates can share their resumes to keerthana.rojanala@vimta.com

 

About the company

Vimta

Industry

Pharmaceuticals

Company Size

501-1000 Employees

Headquarter

Hyderabad

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