Daksh Pharma Pvt. Ltd.

Company Description Msea Pharmaceuticals is located in Ponta Sahib ( manufacturing unit under the Daksh Group). We are committed to providing high-quality medicines to individuals worldwide, with a focus on making healthcare accessible and affordable. Our diverse portfolio of medicines covers various therapeutic areas. We prioritize quality and adhere to stringent regulatory standards to ensure the safety and effectiveness of our products. We are looking for a highly experienced and dedicated professional for the role of QA Head & Documentation at 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 recruits . Regularly conduct quality training sessions to maintain a 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.