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Qa Auditor

Navitas Life Sciences
Navitas Life Sciences
1-3 years
Not Disclosed
Bangalore, India
10 April 21, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing

Job Title: QA Auditor

Department: Corporate Services


Role Overview

The QA Auditor is responsible for conducting audits, ensuring regulatory compliance, and supporting the Quality Management System (QMS). The role involves evaluating processes, managing quality issues, and providing QA guidance to project teams.


Key Responsibilities

1. Audit Execution

  • Conduct audits of projects, systems, processes, and vendors as assigned

  • Assess compliance with regulations, guidelines, customer requirements, and SOPs

  • Prepare and report audit findings in an objective and unbiased manner

2. Compliance & Quality Management

  • Evaluate SOP deviations, quality issues, and complaints

  • Support root cause analysis and development of Corrective and Preventive Actions (CAPAs)

  • Ensure proper documentation and closure of quality issues

3. Audit & Inspection Support

  • Assist in preparation for customer audits and regulatory inspections

  • Support hosting of audits and ensure audit readiness

4. SOP Management

  • Prepare and contribute to SOP development

  • Review and update SOPs to ensure regulatory compliance

5. QA Advisory & Support

  • Provide QA consultancy to project teams on regulatory requirements, guidelines, and SOPs

  • Support implementation and maintenance of the Quality Management System (QMS)

6. Continuous Improvement

  • Participate in and support departmental QA initiatives

  • Contribute to process improvements and quality enhancement activities


Required Skills & Competencies

  • Strong understanding of regulatory requirements and quality standards

  • Experience in audit execution and reporting

  • Knowledge of CAPA processes and root cause analysis

  • Good documentation, analytical, and communication skills


Preferred Experience

  • Experience in clinical trial audits

  • Experience in site investigator audits