Vimta Labs Hyderabad is Recruiting Bioanalytical QA Executives

Vimta Labs Hiring for Food Residues, Nutrition & Water - Analyst & Senior Analyst Roles

Vimta Labs, a renowned name in the pharmaceutical and life sciences industry, is hiring Bioanalytical QA Executives at its Cherlapally, Hyderabad location. This is an exciting opportunity for professionals with 1–3 years of experience to join a dynamic team and contribute to the organization’s quality management systems and regulatory compliance efforts.


About the Role

Designation:

QA Executive – Bioanalytical

Location:

Cherlapally, Hyderabad

Experience Required:

1–3 years

Compensation:

As per industry standards

This role is pivotal in ensuring that the bioanalytical department meets the highest standards of quality and regulatory compliance.


Key Responsibilities

As a Bioanalytical QA Executive at Vimta Labs, your responsibilities will include:

Primary Responsibilities

  • 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 Sponsors requirements. Communicate the findings of the audits to the auditees, Reporting manager and Quality Manager.
  • Review of protocols, Method Validation protocols, Method Validation Reports, Final STPs, SOPs, Calibration data Concentration and statistical data.
  • Perform Internal Quality Audits (IQA) of bioanalytical and other cross functional departments as directed by the Quality Manager.
  • Ensure that the requisite corrective and preventive actions are taken and implemented.
  • Review of Calibration data.

Secondary Responsibilities

  • Issuance of SOPs, forms and other documents and maintaining track of the issued documents, archival of documents as and when required.
Vimta Labs Hiring for Food Residues, Nutrition & Water - Analyst & Senior Analyst Roles
Vimta Labs Recruitment Notification

Qualifications and Skills

Education Requirements:

  • A degree in Pharmaceutical Sciences, Biotechnology, Chemistry, or a related discipline.

Skills and Expertise:

  • Hands-on experience with:
    • In-process audits
    • GXP compliance
    • Protocol review and validation
    • Statistical and calibration data analysis
    • Internal Quality Audits
  • Strong understanding of regulatory guidelines and sponsor requirements.

How to Apply

If you meet the qualifications and are interested in this opportunity, send your resume to:
keerthana.rojanala@vimta.com

Tagged as: Good Clinical Practice (GCP), Pharmaceutical Careers

Upload your CV/resume or any other relevant file. Max. file size: 3 GB.


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