WALK-IN INTERVIEW For Production Quality Control And Quality Assurance NATCO PHARMA LIMITED

WALK-IN INTERVIEW @ NATCO PHARMA LIMITED

SATURDAY, 01st FEBRUARY 2025 @ HYDERABAD

Venue details:

Natco House, Road No 2, Banjara Hills, Hyderabad - 34

Work Location:

Formulation Division Visakhapatnam

Quality Control (QC), Quality Assurance (QA), and Production to ensure the manufacture of safe, effective, and high-quality drugs. Here’s an overview of each department and their responsibilities:

1. Quality Control (QC):

Definition: QC involves testing and evaluating raw materials, in-process materials, and finished products to ensure they meet established quality standards.
Key Responsibilities:
- Conduct physical, chemical, and microbiological tests on raw materials, intermediates, and final products.
- Validate and calibrate analytical equipment.
- Stability testing of products to ensure shelf-life.
- Monitor environmental conditions (e.g., cleanrooms, water, and air quality).
- Generate test reports and ensure compliance with specifications.
Outcome: Identifies and isolates non-conforming materials/products before distribution.

2. Quality Assurance (QA):

Definition: QA ensures that the entire manufacturing process adheres to regulatory and quality standards.
Key Responsibilities:
- Develop, implement, and maintain Standard Operating Procedures (SOPs).
- Conduct internal and external audits.
- Oversee Good Manufacturing Practices (GMP) compliance.
- Review and approve batch manufacturing and packaging records.
- Investigate and resolve deviations and implement Corrective and Preventive Actions (CAPA).
- Manage change control processes.
- Train employees on quality systems and standards.
Outcome: Prevents quality issues by ensuring consistent adherence to procedures.

3. Production Department:

Definition: The production department is responsible for the manufacturing of pharmaceutical products as per regulatory guidelines and approved standards.
Key Responsibilities:
- Manufacturing products according to the approved batch manufacturing records.
- Overseeing the formulation, compounding, and packaging of drugs.
- Maintain production schedules and ensure efficiency.
- Implement GMP guidelines during all production stages.
- Perform in-process checks in collaboration with QC.
- Coordinate with QA for documentation and compliance.
Outcome: Ensures products are manufactured in a safe, effective, and cost-efficient manner.

Collaboration Between Departments:

QC & Production: QC tests the materials and products generated by the production department to ensure compliance with standards.
QA & Production: QA ensures the production team follows SOPs, GMPs, and quality protocols.
QC & QA: Both work together to detect deviations and implement corrective actions to prevent future quality failures.