Quality Control Documentation Assistant

Job Description
Teva Pharmaceutical Industries Limited (TEVA) in Malta is currently looking to recruit a Quality Control Documentation Assistant to join their team on a full-time basis.

Job Role:
The candidate will report to the Finished Goods (FG) Sr Supy and form part of the Quality Control team. The main responsibility is to handle the documentation pertaining to the Quality Control laboratory and to assist the FG Sr Supv in certain duties pertaining to the administration of the respective section. 

This position is based in Bulebel and is on a definite period of 12 months.    

Requirements:

• The ideal candidate must have a good eye for detail and be highly organised, accurate and methodical in his/her work
• Good communication, documentation, and time management skills are necessary
• Applicants should have an Advanced level standard of education or equivalent or an Ordinary level standard of education preferably knowledgeable in science subjects
• The candidate must be computer literate and proficient in Microsoft Office applications.

Teva Pharmaceutical Industries Limited (TEVA):
Teva is a global pharmaceutical leader and the world's largest generic medicines producer committed to improving health and increasing access to quality Health solutions worldwide. Our employees are at the core of our success, with colleagues in over 80 countries delivering the world's largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and we've built a promising pipeline centred around our core therapeutic areas.  We are continually developing patient-centric solutions and significantly growing both our generic and speciality medicines business through investment in research and development, marketing, business development and innovation. This is how we improve health and enable people to live better, healthier lives. Join us on our journey of growth!