Natrix Sciences Ltd. operates an EU cGMP-licensed pharmaceutical facility specialising in the production of generic products. As a Contract Development and Manufacturing Organisation (CDMO), Natrix Sciences focuses on Modified Release Solid Oral Dosage Forms, including powders, granules, and pellets for hard gelatine capsules.

In recent years, the company has expanded its capabilities to support innovative research and development projects within emerging industries. Additionally, Natrix Sciences provides services to ZenPharm Limited, which holds a licence to produce medicinal cannabis and has positioned itself as one of the local leaders in this sector.

This role offers candidates a unique opportunity to utilise their existing quality assurance knowledge within the generic pharmaceutical industry, while expanding their expertise and gaining valuable experience in the medical cannabis industry.

Main Objectives of the Job:

To actively participate in the process of creating and managing an effective Quality Management System.

Specific Duties and Responsibilities of the Job:

To keep a log of all QA documentation, including filing and retrieval.
To register, process, approve and distribute QA documents.
To issue and distribute Standard Operating Procedures (SOPs) and other GMP documents.
To issue batch documentation and compile documents for review and release of batches.
To plan, organise, facilitate and maintain training programs, including training matrix and training files.
To support the maintenance of the change control and deviation processes, including the registration and tracking of follow-up actions.
To register and follow-up supplier complaints.
To support the Quality Risk Management system to ensure that any risks are adequately identified, mitigated and controlled.
To support Production and Quality investigations, root cause analysis and remediation activities.
To assist with the issue and update of Raw Material and Finished Products Specifications.
To assist in the supplier approval process.
To assist in the preparation of Product Quality Reviews (PQRs), Annual Quality Reports (AQRs) and other relevant quality documents.
To participate in continuous improvement projects.

Requirements

To possess an A-Level standard of education, or at least an O-Level standard of education.

Computer proficient with excellent command of the Microsoft Office suite, especially Excel.

Strong written and verbal communication skills in English, with the ability to communicate clearly and effectively.

Experience within the pharmaceutical industry is considered an asset.

The ideal candidate will be capable of working efficiently and effectively, be a good team player and be able to work under pressure. The chosen candidate must exhibit strong interpersonal skills and a willingness to learn continuously, be well-educated and organised, have an eye for detail and have good communication skills.

Quality Assurance Assistant

Job Description