Job Responsibilities

- Maintain and continuously improve the Quality Management System (QMS) for research laboratories.
- Ensure compliance with NABL (ISO/IEC 17025), GLP principles, and other applicable national and international quality standards.
- Prepare, review, and control SOPs, specifications, protocols, reports, manuals, and quality records.
- Plan, conduct, and coordinate internal audits, document audits, and facility inspections.
- Monitor implementation of CAPA, deviations, change controls, risk assessments, and quality investigations.
- Coordinate external audits, accreditation assessments, and regulatory inspections.
- Support maintenance and renewal of NABL accreditation.
- Participate in establishing and implementing GLP-compliant systems for the In Vivo laboratory.
- Review laboratory documentation to ensure data integrity, traceability, and compliance with approved procedures.
- Coordinate training programs related to quality systems, documentation practices, GLP, and regulatory compliance.
- Monitor calibration, qualification, validation, and maintenance records of laboratory instruments and equipment.
- Track quality metrics and prepare management review reports.
- Promote a culture of quality, compliance, and continuous improvement across research laboratories.

Educational experience and requirements:

- M.Sc. or Ph.D. in Life Sciences, Chemistry, Pharmaceutical Sciences,



Biotechnology, Microbiology, Biochemistry, or any relevant scientific discipline.
- 38 years of experience in Quality Assurance within a research laboratory, CRO, pharmaceutical, biotechnology, or analytical testing environment.

Candidates having experience in one or more of the following would be preferred:

- NABL-accredited analytical or microbiology laboratories.
- GLP implementation or maintenance.
- Pharmaceutical or biotechnology R&D.;
- CRO or research organizations.
- Internal auditing and quality system management.
- Laboratory documentation, validation, and regulatory

Preferred Skills:

- Strong understanding of Quality Management Systems.
- Working knowledge of NABL (ISO/IEC 17025) requirements.
- Knowledge of OECD GLP principles and GLP implementation.
- Familiarity with documentation control and data integrity requirements.
- Excellent analytical, organizational, and problem-solving skills.
- Valuable communication and interpersonal abilities.
- Proficiency in Microsoft Office and electronic documentation systems.

How to Apply :

- Write to [email protected] with your detailed resume, cover letter and career aspirations.
- Please mention Application for Quality Assurance in the subject line.
- List three professional references other than your friends and family.

📌 Senior Executive / QA Manager (Haridwar)
🏢 Patanjali Research Foundation
📍 Haridwar