Organisation:

Natrix Sciences Limited is an EU cGMP-licensed pharmaceutical facility specializing in the development and manufacturing of generic medicines. Operating as a Contract Development and Manufacturing Organisation (CDMO), Natrix focuses on Modified Release Solid Oral Dosage Forms - including powders, granules, and pellets - intended for filling into hard gelatin capsules and tablets.

With a growing reputation for excellence, Natrix has also positioned itself as a strategic partner in innovative research and development projects, particularly in emerging and dynamic industries.

In addition to its core pharmaceutical operations, Natrix Sciences provides specialized services as ZenPharm Limited, a licensed producer of medicinal cannabis. ZenPharm is well-placed to become a local industry leader, and this collaboration offers unique cross-sector experience.

Opportunities for Professional Development:

The Production department at Natrix Sciences offers opportunities for professional growth within a dynamic and ambitious team. Candidates joining the company will become part of a team driven by innovation and excellence. Consequently, we require motivated, committed, and resilient team players who can also work on their own initiative.

Specific Duties and Responsibilities:

The successful candidate will be responsible for:

To dispense raw materials.
To perform the processes of various pharmaceutical solid dosage forms and to operate all machinery required for these processes.
To clean all the equipment/area used in the above processes
To participate in pharmaceutical production/packaging in the cGMP facility according to the exigencies of Natrix Sciences Ltd.
To keep the highest quality considerations always in mind during all production / packaging processes whilst striving to achieve the necessary output.
To report any deviations from SOPs/processes and cGMP guidelines.
To actively participate in training sessions (receiving and delivering)
To assist other employees in other departments in fulfilling the common quality goals.
To follow all applicable safety procedures.
Ensuring GMP compliance as per local procedures and EudraLex Volume 4 GMP guidelines.

Requirements:

An ordinary level standard of education.
Good written and verbal communication skills in both English and Maltese.
Possession of an EU work visa.

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

Production Operator

Job Description