Quality Assurance Specialist

1 day ago

Chandigarh, Chandigarh, India Daksh Pharma Pvt. Ltd. Full time ₹ 12,00,000 - ₹ 36,00,000 per year

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.

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