Consultant Pathologist - Kota

Role : Consultant Pathologist

Department : Customer Success (Operations)

Reporting To : Laboratory Director

Role Definition

The Consultant is responsible for ensuring high-quality diagnostic reporting, end-to-end technical supervision, adherence to NABL / ISO standards, and timely clinical correlation with Clinicians. The role involves oversight of pre-analytical to post-analytical processes, technical staff training, equipment calibration validation, and ensuring excellence in turnaround time (TAT), report accuracy, and patient & clinician satisfaction.

Deliverables

Diagnostic Excellence

Regulatory & Quality Compliance

Clinician & Corporate Parties Satisfaction

Team Enablement

Stakeholder Engagement

Responsibilities

Diagnostic Oversight & Reporting

Personally validate and sign out pathological results within defined TAT, ensuring clinical correlation wherever applicable.

Release critical, high-value, high-risk reports with history-backed interpretation.

Ensure reporting of critical values within 30 minutes through Helpdesk coordination and documentation of escalation.

Review repeat testing, delta checks, or Clinician queries before finalizing reports.

Resolve escalated clinician or B2B partner queries related to report delay, interpretation, or values.

Laboratory Operations Management

Monitor daily workflow (sample registration to reporting) to ensure seamless processing without bottlenecks.

Conduct morning huddles with technical team for daily work allocation, sample volume trends, pending TAT cases.

Define shift plans, ensure break management, and redistribute manpower to high-load areas.

Track hourly dashboards to monitor sample inflow, pending batches, machine utilization.

Conduct daily walk-throughs of sample reception, processing, storage, and disposal areas.

Maintain cold chain and monitor temperature logs of refrigerators, centrifuges, and transport boxes.

Coordinate with logistics on delayed samples and prioritize urgent cases for immediate processing.

Optimize TAT and batch processing to reduce costs. Monitor sample rejection or re-run trends and reduce wastage-related expenses.

Keep manpower costs within budgeted limits through efficient shift rotation and overtime control.

Prepare and present weekly Laboratory Operations Performance dashboards on CSAT, sample volume, rejection, TAT, QC, to HO Team.

Quality Management & Compliance

Daily IQC review with Laboratory / Quality Manager— document, sign, and flag any trend shift.

Review EQAS data, scoring, and discussion of non-conformities with root cause analysis.

Approve monthly QC summary, LJs charts, and logbook updates.

Review and sign off on calibration / maintenance logs for all analyzers.

Ensure reagent logs, expiry management, and kit validation documentation are updated.

Conduct monthly internal audits; verify SOP compliance, sample logs, and result traceability.

Ensure CAPA closure within 7 working days of any non-compliances or deviation.

Ensure SOP version control and display; conduct annual policy review with Central QA team.

Pre-Analytical & Sample Management

Supervise specimen collection quality, labeling accuracy, transport condition, and rejection criteria compliance.

Conduct random audits of sample adequacy and SOP adherence by phlebotomy and accessioning teams.

Ensure timely centrifugation of time-sensitive parameters

Coordinate with logistics and floor teams for timely sample receipt and prioritization of samples.

Conduct monthly training for high-error (Pre Analytical Non Compliances) phlebotomy / branch teams.

Technical Team Training & Development

Conduct structured induction and monthly training programs on SOPs, test parameters, compliances, and QMS updates.

Review competency assessments, technical error trends, and initiate re-training wherever needed.

Lead scientific case discussions and knowledge sessions to upskill team members.

Consumables, Reagents, Instrumentation & Infrastructure Oversight

Review monthly consumption patterns of reagents, kits, and consumables against test volume. Validate monthly indents before purchase approval; avoid overstocking / stockout.

Monitor machine downtime, AMC status, and repair costs; escalate cost overages to Central Team.

Review daily maintenance, calibration logs, and error flags on automated machines

Approve validation protocols for new test methods or equipment introduced in the laboratories.

Ensure zero downtime and contingency planning for analyzers through AMC adherence and backup systems.

Clinical Interface & Doctor Engagement

Address Corporate Parties and clinician queries, including result clarification, discrepancy resolution, and diagnostic suggestions.

Maintain communication with top KOLs & A category customers : key discussions, complaints, follow-ups.

Participate in regional CMEs, RTMs, and case-based learning sessions with the medical community.

Build credibility for DBCL services through scientific communication and evidence-based advice.

Skills Required

Validation, Equipment Calibration, sample management , Internal Audits