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Executive-Quality Assurance

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Onsite

Executive-Quality Assurance

Lifecell

Executive-Quality Assurance

Skills

Testing & QAInternal AuditCompliance

1 month ago

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Important information


Contract type:

Permanent

Salary:

₹50,000 / year

Location:

Chennai, Tamil Nadu, India

Work mode:

Onsite

Published on:

23 September 2026

What they need


We are seeking an operational Quality Assurance (QA) Specialist to verify, audit, and enforce day-to-day adherence to established Standard Operating Procedures (SOPs) across our wet-lab and bioinformatics workflows. this role focuses on conducting process audits, monitoring routine operational compliance, handling deviations, and maintaining our active NABL (ISO 15189) and CAP accreditations

Key Responsibilities

  • Perform regular on-floor process audits across molecular testing (extraction, qPCR, NGS) and bioinformatics analysis to ensure staff execute procedures strictly per approved SOPs.
  • Verify that bench scientists and bioinformaticians accurately maintain operational logs, run-execution records, and chain-of-custody documentation.
  • Monitor sample hand-offs, instrument runs, and data transfer checkpoints to catch standard operating variances early.
  • Coordinate and assist with routine NABL (ISO 15189) and CAP surveillance audits, re-assessments, and proficiency testing (PT) submissions.
  • Conduct internal audits following established checklists to assess continuous readiness for external regulatory inspections.
  • Manage non-conformance logging, coordinate with technical teams to execute Root Cause Analyses (RCA), and track Corrective and Preventive Actions (CAPA) to completion.
  • Review quality control (QC) check outputs for wet-lab steps (e.g., DNA/RNA yield, library prep QC) and bioinformatic pipelines (e.g., FASTQ metrics, coverage depth, BAM/VCF status checks).
  • Audit instrument maintenance logs, reagent lot-to-lot verification records, and calibration status before technical sign-offs.

Experience required

  • 23 years working in an accredited clinical or diagnostic laboratory environment.
  • Direct experience performing process adherence checks and internal audits against established SOPs.
  • Familiarity with molecular workflows (PCR, Sanger, NGS) and basic bioinformatic output files (FASTQ/BAM/VCF).
  • Hands-on involvement maintaining NABL (ISO 15189) or CAP compliance.

Kindly share your resume to : [email protected]

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