Stability Analyst

Teva Pharmaceuticals in Malta is looking to recruit a Stability Analyst to join their Quality Control Lab Team on a full-time basis. Reporting to the Stability Coordinator, this position is based in Bulebel.

Main Responsibilities include:

• Reviewing all PS data;
• Compiling of stability protocols and reports;
• Compiling of supporting documentation and logistical support for outgoing method transfers of stability studies;
• Coordinate the necessary reservation and preparation of Production samples for Stability studies.

The Applicant: 
The ideal candidate should:

• Have a good eye for detail, be highly organised, accurate, and methodical in his/her work;
• Good communication, documentation, and time management skills are necessary;
• Applicants must possess a diploma in Applied Science or a Degree in Science subjects (Chemistry, Biology, or Medical Laboratory Science). Applicants having two Advanced Level qualifications in Science subjects (including Chemistry) will also be considered;
• Previous laboratory experience is considered an asset, although full training will be provided;
• The candidate must be computer literate and proficient in Microsoft Office applications.