Skip to main content
cGxPjobs.com
Log inSign up

Back

Jobs at Vimta Labs Ltd

Showing 6 JobsSort by:

QA Manager, GLP

  • Vimta Labs Ltd

    • On-site
    • Hyderabad, TG

Project Manager, Sponsor Programs

  • Vimta Labs Ltd

    • On-site
    • Hyderabad, TG

Scientist, Environmental Sciences

  • Vimta Labs Ltd

    • On-site
    • Hyderabad, TG

Analyst — Food & Water Testing

  • Vimta Labs Ltd

    • On-site
    • Hyderabad, TG

Group Leader — Clinical Operations

  • Vimta Labs Ltd

    • On-site
    • Hyderabad, TG

Senior Scientist — Bioanalytical (LC-MS/MS)

  • Vimta Labs Ltd

    • On-site
    • Hyderabad, TG

1–6 of 6 jobs

QA Manager, GLP

  • Vimta Labs Ltd

  • Hyderabad, TG
Open in New Tab

On-site

Not Disclosed

Contract Research/Testing

Quality

  • Posted on:
  • No. of Vacancies:

Job Description

Summary

As a QA Manager — GLP, you will partner with cross-functional teams to deliver measurable impact within the Vimta scientific ecosystem. This role blends hands-on execution with stakeholder collaboration, contributing to programs that advance pharmaceutical research, clinical insight, and quality assurance for clients across India and global markets.

Responsibilities
  • Review technical documentation, quality records, and reports for accuracy and compliance.
  • Coordinate with laboratory operations, QA teams, and scientific leadership to resolve quality issues.
  • Ensure project timelines, quality standards, and regulatory requirements are consistently met.
  • Identify quality risks and implement corrective measures to prevent recurring issues.
  • Prepare quality reports and maintain audit-ready documentation.
  • Mentor junior QA staff, review their work, and support training and competency development.
  • Monitor team workloads, escalate critical issues, and ensure timely closure of quality activities.
  • Drive continuous improvement in quality processes and compliance practices.
Qualifications
  • Educational qualification appropriate to the role (see the Education line in the role-details panel).
  • Demonstrated experience in the relevant domain, including hands-on familiarity with industry-standard tools, instruments, or platforms.
  • Strong written and verbal communication; comfortable engaging with scientific peers, regulators, and clients alike.
  • A bias for ownership, structured problem-solving, and clear documentation — with a quality-first mindset.
Education

Degree

Masters

Specialization

Science/Pharma
Experience:

8-10 yrs

  • Skills:
  • GLP
  • Quality Assurance
  • Technical documentation
  • Regulatory Compliance
  • Quality Records and Report Review
  • GLP and Regulatory Compliance
  • Job Type:
  • Full-time
  • Shift Type:
  • 8 hour shift
  • Monday to Friday
  • Day shift

Compensation

  • Benefits:
  • Medical, Dental, Vision
  • Additional:
  • Base Salary
  • Bonus

Job ID:

CGXP_26_28868

© cGxP Tech, Inc. All rights reserved.