Junior Quality Assurance Supervisor

Tawteen

Job details

Academic qualification: Diploma in Pharmacy, Chemistry, Chemical Engineering, Biotechnology, or any related field.

Job objective:

Ensure compliance of all manufacturing and packaging operations with Good Manufacturing Practices (GMP), regulatory requirements, and company quality standards, by conducting in-process inspections, monitoring plant activities, and providing immediate quality support.

Job duties

1- In-process Quality Assurance (IPQA)

Perform routine checks during manufacturing and packaging operations in accordance with BMR/BPR requirements and standard operating procedures.

Verify production line clearance, equipment cleanliness, and raw material weights before starting production (including solid, liquid, and API distribution activities).

Perform production conformance and monitor critical process parameters to ensure product quality.

Collect in-process, final product, stability, control, process validation, cleaning validation, hold-time, and rinse samples for analysis (including total organic carbon testing where applicable).

Perform verification activities in accordance with approved verification protocols.

Calibration and maintenance of IPQA instruments and scales.

2- Quality control during manufacturing processes

Compliance with Good Manufacturing Practices (GMP), Standard Operating Procedures (SOPs) and safety guidelines in all production areas (including the main plant and the beta-lactam facility).

Conduct daily factory floor walks to monitor compliance with Good Manufacturing Practices (GMP) and environmental standards (temperature, humidity, differential pressure).

Document and report deviations, non-conformities, and anomalies noted during operations.

Preparing and updating IPQA specifications and Standard Operating Procedures (SOPs).

3- Documentation and reports

Review and verify manufacturing and packaging records for completeness, accuracy, and compliance with standards.

Maintain immediate documentation of observations, deviations, corrective actions, and CAPAs.

Assist in preparing deviation reports, investigation reports and documenting quality incidents