Teva Quality Assurance Group Specialist 

Lithuania, Vilnius County 

352665065

• 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).

• 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).

• Salary range of 2 300 – 2 600 Euro gross monthly,
• Benefits package: health and accident insurance, additional health and vacation days (for worked years),
• Highly professional team and organizational culture with strong values,
• Personal and professional development within the company,
• Work model supporting work life balance,
• Employee rewards and recognition programs, events and social activities.

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