Quality Control Technician - Analytical Lab

Who we are

Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world’s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we’re always looking for new ways to continue making a difference, and new people to make a difference with.

The opportunity

In this role, you will play a vital part in ensuring the quality and safety of our products by conducting routine testing on samples from our production process. Your work will directly contribute to maintaining our high-quality standards and compliance with GMP regulations.

This is an excellent opportunity for detail-oriented professionals who are passionate about quality control and analytical chemistry. 

How you'll spend your day

• Routine Testing finished products and in-process control samples according to SOP and as per the committed time lines
• Handle quality management system like Deviations and Out of specification results (Phase 1 investigation)
• Writing, review and approval of test results
• Maintain adherence to corporate policies and appropriate regulations through actions and decisions
• Active participation in advanced problem solving, root cause analysis, troubleshooting, interpretation/consultation, verification of quality and test results discussions
• First-line Troubleshooting of laboratory equipment
• Work a shift pattern (24/7)

Your experience and qualifications

• MLO+ / HBO / Bachelor degree in analytical chemistry/pharmacy or equivalent experience
• Knowledge and familiarity with the use of Pharmacopoeia methods
• A strong analytical oriented mindset
• Experience with working in a pharmaceutical environment
• Experience with analytical techniques like, UPLC/HPLC, TOC, PSD, etc.
• Good knowledge of Pharmaceutical quality systems and production processes 
• Experience & exposure to work in regulatory environment as well as Regulatory Audit like EU cGMP inspection , US-FDA, ANVlSA
• Team player
• Strong can-do mentality
• Results oriented

Function

Sub Function

Already Working @TEVA?

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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.

Pre-Employment Screening

Teva will carry out appropriate verification and legally permitted vetting prior to the confirmation of any offer of employment. More information on this verification and vetting will be provided if you reach this stage of the application process