Quality Assurance Specialist

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.

QA Head & Documentation

Position Details

• Designation:

   QA Head & Documentation

• Experience:

   Minimum 20 years in Pharma (Formulations / Manufacturing / Exports)

• Location:

   Panchkula, Haryana

• Industry:

   Pharmaceuticals – Domestic & Export

Key Responsibilities

QA Head & Documentation

• 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.