Quality Assurance Group Specialist

Teva

Vilnius, Lithuania

Join a global leader in pharmaceuticals and play a key role in ensuring the highest quality standards in drug manufacturing. In this role, you’ll collaborate with international teams, drive innovation in quality processes, and contribute to life-changing medicines. At Teva, we care about your growth, support each other, and make work truly fulfilling.

How you’ll spend your day

Manage batch release documentation,
Collaborate with the international Teva team on DP testing and release,
Review batch manufacturing, analysis, and MS&T protocols,
Investigate and resolve laboratory and manufacturing deviations,
Oversee corrective and preventive actions (CAPA), complaints, and change control,
Monitor KPIs and work with QC to optimize product cycle times,
Review stability data and manage stability documentation,
Ensure quality compliance on the production floor (Quality Shop Floor),
Review QC analytical testing (QC AT Review).

Your experience and qualifications

University degree in Pharmacy or Natural Sciences (Biology, Biochemistry, Biotechnology) or equivalent,
1-2 years of experience in a GMP-regulated environment (laboratory, production, or quality-related roles),
Familiarity with regulatory requirements and international collaboration is a plus,
Strong analytical skills and attention to detail,
Good English communication skills (written and spoken),
Ability to manage multiple tasks and work effectively in a team,
Enthusiastic, well-organized, and eager to learn and grow,
Proficiency in Microsoft Office (Word, Excel, PowerPoint, databases).

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