Job Description

Qualification: B.Sc/M.Sc Chemistry

Experience: 1 to 2 Years

Job Summary:

- Responsible for ensuring compliance with regulatory requirements and Positive Laboratory Practices (GLP) within the pharmaceutical industry, particularly for analytical laboratory testing and documentation. The role involves preparation and review of Standard Operating Procedures (SOPs), management of change controls, deviations, incidents, and Corrective and Preventive Actions (CAPA), along with reviewing GLP-related documents to maintain quality standards and regulatory compliance.

Key Responsibilities:

- Prepare, review, and revise Standard Operating Procedures (SOPs) in accordance with applicable regulatory requirements and internal quality standards.
- Manage and monitor Change Control procedures to ensure proper evaluation, approval, implementation, and documentation of changes.
- Handle deviation management, including investigation, root cause analysis, documentation, and follow-up of corrective actions.
- Record, investigate, and document incidents in accordance with established quality procedures.
- Initiate, review, and monitor Corrective and Preventive Actions (CAPA) to ensure effective resolution of quality issues.




- Review Good Laboratory Practice (GLP) documents and analytical laboratory records to ensure accuracy, completeness, and compliance.
- Ensure compliance with applicable regulatory requirements, quality management systems, and internal laboratory procedures.
- Maintain proper documentation and records to support internal audits, regulatory inspections, and quality assessments.
- Coordinate with laboratory personnel to ensure adherence to approved procedures and quality standards.
- Support continuous improvement initiatives to strengthen documentation practices and maintain a state of regulatory compliance.

Required Knowledge and Skills:

- Working knowledge of Quality Assurance practices in the pharmaceutical industry.
- Knowledge of regulatory requirements applicable to analytical laboratory testing and documentation.
- Experience in SOP preparation, review, and revision.
- Understanding of Change Control, Deviation Management, Incident Reporting, and CAPA procedures.
- Knowledge of GLP documentation review and compliance requirements.
- Good documentation, communication, analytical, and problem-solving skills.

📌 Qa Analyst (Ahmedabad)
🏢 Vaibhav Analytical Services
📍 Ahmedabad