Remote/Hybrid QA Job Opening at ICON plc – BSc Apply Now

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"Unlock Your Future: Quality Assurance Auditor I Role at ICON plc!"

ICON plc Remote Pharma Jobs – Apply For QA Role

Position: Quality Assurance Auditor I

Location: Bangalore, Chennai, Bengaluru

Job ID: JR125858

Category: Quality Assurance | ICON Full Service & Corporate Support

Work Arrangement: Hybrid (Office/Remote)

About the Role

Position: Quality Assurance Auditor I – Chennai/Bangalore (Remote or Hybrid Working)

ICON plc is a world-leading healthcare intelligence and clinical research organization. We are proud to foster an inclusive environment driving innovation and excellence. Join us in shaping the future of clinical development.

This role is part of the Tech QA team, supporting GxP Risk Impact Assessments and Validation Reviews. The position involves reviewing ICON and vendor-delivered computerized systems and technology platforms. If you have knowledge of CSV, Vendor Qualification, and some experience in operational areas (e.g., IRT, Medical Imaging, Clinical Trials), this could be the ideal opportunity for you.

What You Will Be Doing:

  • Assisting in the development and implementation of quality assurance processes and procedures to support clinical trial activities.
  • Conducting routine quality assessments and audits to ensure adherence to regulatory standards and guidelines.
  • Collaborating with project teams to identify and address quality issues and implement corrective actions as needed.
  • Participating in the review and approval of documentation related to clinical trial operations and quality management systems.
  • Contributing to the maintenance of quality assurance documentation and records.

Your Profile:

Education: Bachelor’s degree in Life Sciences, Pharmacy, or a related field (advanced degree preferred).

Experience: Previous experience in quality assurance within the pharmaceutical, biotechnology, or CRO industry is preferred but not required.

Knowledge: Basic understanding of regulatory requirements and guidelines governing clinical trials (e.g., ICH-GCP, FDA regulations).

Skills:

  • Strong attention to detail and organizational skills.
  • Ability to prioritize tasks effectively.
  • Excellent communication and interpersonal skills.
  • Ability to work collaboratively with cross-functional teams and stakeholders.

APPLY ONLINE HERE

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