Quality Assurance Group Specialist

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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