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Quality Control Laboratory Manager
Actively Reviewing
Bio-State Consulting
Job Description
Job Summary
We are looking for a dedicated and detail-oriented QC Personnel to ensure compliance with Quality Management Systems (QMS), NABL requirements, and ISO/IEC 17025 standards. The candidate will be responsible for audit preparation, calibration control, CAPA management, risk assessment, documentation, and supplier evaluation to maintain high-quality laboratory and regulatory standards.
- Maintain QMS documents, SOPs, and compliance records.
- Prepare for NABL and internal audits.
- Manage calibration records and validation reports.
- Handle CAPA, risk assessment, and non-conformities.
- Conduct internal audits and follow corrective actions.
- Coordinate staff training and competency records.
- Ensure compliance with ISO/IEC 17025 and regulatory requirements.
- Monitor supplier quality and approval processes.
- Participate in proficiency testing and management review meetings.
- Bachelor’s Degree in Biomedical Engineering, , Biotechnology, or related field.
- 3–5 years of experience in laboratory quality systems or medical device regulations.
- Knowledge of ISO/IEC 17025, NABL standards, CAPA, internal audits, and MRM processes.
- Strong documentation, analytical, and communication skills.
- Experience in audit handling and regulatory documentation.
- Good understanding of quality assurance processes.
- Ability to work independently and manage compliance activities efficiently.
- Strong attention to detail and problem-solving abilities.
Location : Faridabad
Required Skills
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