QA Head &
Documentation

By dakshadmin / October 3, 2025

We are looking for a highly experienced and dedicated skilled for the role of QA Head &
Documentation at our pharmaceutical manufacturing unit in Panchkula, Haryana. This is a senior leadership chance 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