Quality Control Analyst - Quality Control jobs in Malta - March 2024
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Quality Control Analyst

Teva Pharmaceutical Industries Limited (TEVA) , South of Malta

Published on 21 Jan 2021

Expired on 19 Feb 2021


Teva Pharmaceuticals in Malta is looking to recruit a Quality Control Analyst to join their team within the QC Laboratory Team on a full-time basis. The position will be reporting to the Raw Materials/Finished Goods Supv. This position is based in Bulebel and is on a two-shift 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.

Teva Pharmaceuticals Industries Limited:
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 centered around our core therapeutic areas.  We are continually developing patient-centric solutions and significantly growing both our generic and specialty 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!

time
Full Time
Job Type
experience
Entry (0-12 months), Intermediate (1-3 years)
Experience Level
category
Quality Control
Category
industry
Pharmaceuticals
Industry


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