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Quality Assurance Specialist

Date: Sep 23, 2022

Location: Vilnius, LT, 01100

Company: Teva Pharmaceuticals

Who are we?

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!

Job Description

We are currently looking for a Quality Assurance Specialist for our manufacturing site in Vilnius.

Main purpose of the role: ensure Company’s GMP compliance with regulated activities 

The person will be directly reporting to Quality Assurance Manager

Type of the contract: permanent

What you will be doing?

•    Batch release documentation management;
•    Work with international Teva team related to Drug Products (DP) testing and release;
•    Review batch manufacture protocols, analysis protocols, Manufacturing Site & Technologies (MS&T) protocols;
•    Investigation and troubleshooting of laboratory, manufacturing deviations corrective and preventive actions, complaints and change control Management; 
•    KPIs management, collaboration with Quality Control (QC) for products cycle time management;
•    Stability review and documentation management;
•    QC Computerized Systems Audit Trail review.

What you will need? Your profile

•    University degree qualified in pharmacy or natural sciences (biology, biochemistry, biotechnology); 
•    Previous work experience with regulatory requirements, work in laboratory, manufacturing, work with international team;
•    Work experience in TW DB, EDMS Glorya, SAP N20;
•    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;
•    Strong drive for results;
•    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).
•    Fluent Lithuanian, very good English written and verbal communication skills

Why Teva?

•    Salary range of 1900 - 2200 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



Sub Function

Manufacturing Quality Assurance

Already Working @TEVA?

If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site

The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.

Teva’s Equal Employment Opportunity Commitment

Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws.