QA Head &

- Documentation

By dakshadmin / October 3, 2025

We are looking for a highly experienced and dedicated professional for the role of QA Head &

- Documentation at our pharmaceutical manufacturing unit in Panchkula, Haryana. This is a senior leadership opportunity for professionals with 20+ years of experience in pharmaceutical quality assurance, documentation, and compliance.

Position Details

- Designation: QA Head &
- Documentation

- Experience: Minimum 20 years in Pharma (Formulations / Manufacturing / Exports)

- Location: Panchkula, Haryana

- Industry: Pharmaceuticals – Domestic &

- Export

Key Responsibilities

As the QA Head &

- Documentation, you will be responsible for ensuring the highest standards of quality, compliance, and operational excellence across our manufacturing and export units.

- Leadership &
- Oversight

- Oversee the entire manufacturing unit’s quality assurance activities, ensuring compliance with WHO-GMP and other global regulatory standards.

- Monitor day-to-day operations, ensuring smooth functioning of the QA systems.

- Documentation &

- Compliance

- Supervise all manufacturing unit documentation, export documentation, and compliance reports.

- Maintain and review batch manufacturing records (BMRs), standard operating procedures (SOPs),



and export regulatory documentation.

- Ensure timely submission and accuracy of daily QA reports and audit records.

- Audits &

- Regulatory Affairs

- Lead internal and external audits with regulatory authorities.

- Ensure the unit is always prepared for inspections from domestic and international agencies.

- Training &

- Development

- Develop and implement training protocols for QA staff, production team, and recent recruits.

- Regularly conduct quality training sessions to maintain compliance culture across departments.

- Reporting &

- Review

- Oversee daily quality assurance reports, deviations, and CAPA (Corrective &

- Preventive Actions)

.

- Present quality and compliance updates to senior management.

Candidate Profile

- Minimum 20 years of experience in Quality Assurance, Documentation, and Regulatory Compliance within the pharmaceutical industry.

- Strong knowledge of domestic and export regulatory frameworks.

- Proven ability to lead large QA teams and handle multi-unit operations.

- Hands-on expertise in manufacturing documentation, audits, and training protocols.

- Excellent communication, leadership, and decision-making skills.

📌 QA Head & Documentation (Industrial Area)
🏢 Daksh Pharmaceuticals
📍 Industrial Area