QC Manager

Job Details

• *Job Title:** QC Head / QC Manager
• *Company:** AVM Labs
• *Job Location:** Coimbatore, Tamil Nadu
• *Experience:** 3–4 Years
• *Qualification:** M.Sc. Biochemistry / Ph.D. Biochemistry
• *Salary:** ₹5–7 LPA
• *Employment Type:** Full\-Time
• *Work Location:** In Person

Job Description

AVM Labs is looking for an experienced and hands\-on QC Head to lead the Quality Control function and ensure high standards of quality, accuracy, reliability, regulatory compliance, and laboratory operations.

The ideal candidate should have an M.Sc. or Ph.D. in Biochemistry with relevant experience in Quality Control, diagnostic laboratories, healthcare, or a related industry. The candidate will be responsible for managing QC activities, handling end\-to\-end NABL accreditation requirements, monitoring EQAS performance, investigating deviations and OOS results, maintaining quality documentation, and leading the QC team.

Key Responsibilities1\. Quality Control \& Laboratory Management

• Lead and manage the Quality Control team and day\-to\-day QC activities.
• Plan, organize, and monitor laboratory testing and quality control processes.
• Ensure accurate, reliable, and timely testing and reporting.
• Establish, review, and maintain QC procedures, specifications, and quality standards.
• Review and approve QC test results, reports, and related documentation.
• Monitor QC performance and ensure adherence to approved procedures.

2\. NABL Accreditation \& Compliance

• Handle end\-to\-end NABL accreditation activities and maintain compliance with applicable NABL requirements.
• Prepare, review, and maintain NABL documentation, quality manuals, SOPs, and records.
• Coordinate NABL assessments, audits, surveillance visits, and renewals.
• Ensure timely closure of audit observations and non\-conformities.
• Monitor compliance with applicable ISO 15189 requirements and laboratory quality standards.
• Coordinate with internal departments to ensure continuous accreditation readiness.

3\. EQAS \& Quality Monitoring

• Monitor and manage External Quality Assurance Scheme (EQAS) activities.
• Coordinate EQAS sample processing, result submission, and performance evaluation.
• Review EQAS reports and identify deviations or performance issues.
• Implement corrective actions for unsatisfactory EQAS performance.
• Monitor internal quality control (IQC) and external quality control performance.
• Maintain EQAS records and ensure timely completion of related activities.

4\. CAPA \& Deviation Management

• Investigate Out\-of\-Specification (OOS) results, deviations, and non\-conformances.
• Identify root causes and implement appropriate Corrective and Preventive Actions (CAPA).
• Monitor CAPA effectiveness and ensure timely closure.
• Maintain deviation, non\-conformance, and CAPA records.
• Ensure proper documentation and follow\-up of quality\-related issues.

5\. Equipment \& Documentation Management

• Ensure proper calibration, maintenance, and qualification of laboratory equipment.
• Maintain accurate QC records, documentation, and data integrity.
• Monitor and update LJ (Levey\-Jennings) charts for internal quality control.
• Review LJ charts, identify trends, shifts, and quality control failures, and initiate corrective action.
• Ensure proper handling, storage, and documentation of laboratory samples and materials.
• Maintain equipment records, calibration reports, and quality documentation.

6\. Team Management \& Audits

• Train, mentor, and develop QC team members.
• Monitor team performance and ensure adherence to laboratory procedures.
• Coordinate with QA, Laboratory Operations, R\&D, and other departments on quality\-related matters.
• Support internal, external, customer, and regulatory audits.
• Address audit observations and ensure implementation of corrective actions.
• Identify opportunities for continuous improvement in QC processes.
• Prepare and review QC\-related reports, records, and performance metrics.

Required Qualifications

• **M.Sc. Biochemistry / Ph.D. Biochemistry – Mandatory.**
• 3–4 years of relevant experience in Quality Control.
• Experience in diagnostic laboratories, healthcare, pharmaceutical, biotechnology, or related industries preferred.
• Strong knowledge of laboratory testing and QC procedures.
• Practical experience in NABL accreditation and ISO 15189 requirements.
• Knowledge of EQAS, IQC, and LJ chart monitoring.
• Good understanding of quality systems, documentation, and data integrity.
• Knowledge of GMP/GLP and applicable regulatory requirements.
• Experience in OOS, deviation investigation, root cause analysis, and CAPA.
• Experience in laboratory equipment calibration, maintenance, and qualification.
• Strong team leadership and people management skills.

Preferred Skills

• Quality Control Management
• Laboratory Quality Control
• End\-to\-End NABL Accreditation
• ISO 15189 Compliance
• EQAS Management
• IQC \& LJ Chart Monitoring
• Quality Management Systems
• GMP / GLP
• OOS Investigation
• Deviation Management
• CAPA \& Root Cause Analysis
• Data Integrity
• Laboratory Documentation
• Equipment Calibration \& Qualification
• Audit Management
• Team Leadership
• Process Improvement
• Analytical \& Problem\-Solving Skills

Ideal Candidate

The ideal candidate will be a hands\-on, analytical, and result\-oriented Biochemistry professional with strong leadership capabilities and practical knowledge of laboratory quality systems.

The candidate should be capable of leading the QC team, managing end\-to\-end NABL accreditation, monitoring EQAS performance, maintaining LJ charts, handling CAPA and deviations, supporting audits, and ensuring consistent accuracy, reliability, and compliance in laboratory operations.

Salary

• *₹5–7 LPA**, based on qualification and experience.

Benefits

• Cell Phone Reimbursement
• Provident Fund

• *Interested candidates can apply with their updated CV.**

Pay: ₹500,000\.00 \- ₹700,000\.00 per year

Benefits

• Cell phone reimbursement
• Paid sick time
• Paid time off
• Provident Fund

Work Location: In person