Teva Quality Assurance Group Specialist 

Lithuania, Vilnius County 

820521992

• Batch release documentation management;
• Work with international Teva team related to DP testing and release;
• Review batch manufacture protocols, analysis protocols, MS&T protocols;
• Investigation and troubleshooting of laboratory, manufacturing deviations corrective and preventive actions, complaints and change control Management;
• KPIs management, collaboration with QC for products cycle time management;
• Stability review and documentation management;
• Quality shop floor;
• QC AT review.

• University degree qualified in pharmacy or natural sciences (biology, biochemistry, biotechnology);
• Work experience in GMP requirement;
• Previous work experience in the same position, experience with regulatory requirements, work with international/global team, in laboratory, production;
• Very good English written and verbal communication skills;
• Strong drive for results;
• Projects/process management experience is an advantage;
• Ability to work on multiple projects and tasks;
• Proven ability to effectively collaborate with internal and cross-functional teams, as well as external parties, in a fast-paced and complex environment;
• Strong analytical skills;
• Exceptional interpersonal skills and good judgment;
• Flexible, dynamic, highly energetic and very well organized;
• Highly proficient in the following software programs: (Word, Excel, PowerPoint, databases).

• Salary range of 2000 – 2400 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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