Quality Analyst

The opportunity

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

How you’ll spend your day

• Performing incoming control of raw materials, process aids, and packaging materials used for production of active pharmaceutical ingredients 
• Working under requirements of Good Manufacturing Practice
• Sampling and testing of samples according to the requirements of standard operating procedures, specifications, and protocols
• Documenting and evaluating the results of analyses according to specifications
• Working with analytical equipment and computer software used in the process
• Working with chemical reagents and standards
• Preparing standard operating procedures for analytical and control methods, equipment, devices and other documentation
• Selection and introduction of new analytical equipment to the Quality Control laboratory
• Preparing of method validation protocols, carrying out validation of methods, and drawing up final reports

Your experience and qualifications

• Bachelor or master degree in chemistry, biochemistry, bioengineering or related field
• Knowledge of Lithuanian and English languages
• Good understanding of MS Office etc.
• Analytical thinking and problem solving abilities
• Experience of work with hazardous chemicals would be an advantage
• Experience of work with FT-IR, Raman spectroscopy would be an advantage 
• Knowledge of GMP standards would be an advantage 
• Intrinsically motivated, accountable and committed to professional development
• Ability to work as part of a multi-disciplinary team

Enjoy a more rewarding choice

• Salary range of 1800 – 2300 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

Pre-employment verification

All job offers at Teva Lithuania are preceded by pre-screening candidates. In the case of all candidates who have passed to the final stage of recruitment, verification of the data provided in the recruitment process will be carried out, if deemed necessary. More detailed information will be provided to candidates prior to the verification process.

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. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.