Quality Control Analyst

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

The Position:
The position forms part of the QC Laboratory Team. Main responsibilities include sampling and testing of raw materials, finished products, microbiology, or stability samples using qualified laboratory equipment while ensuring compliance with cGMP, company procedures, EH & S regulations as well as Pharmacopoeial and in-house standards and specifications.

The Applicant:

• The ideal candidate must have a good eye for detail, be highly organized, 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.

Already Working @TEVA?
If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply Internal Career Site. The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.

Teva’s Equal Employment Opportunity Commitment:

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