Quality Control Analyst

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

Role Purpose: Performs testing not only of raw materials and drug products, maintenance and calibration of analytical instruments, prepares standard and sample solutions and maintains appropriate records. Carry out checks of record documentation. Areas of Impact: Perform all-types analyses Control record documentation Knowledgeable and experience with laboratory systems Job Aspect: Conducts non-conformance tests of manufactured, packaged or tested product Prepares and monitors quality statistics and report Performs stability program management, analyses, inspection, and tests of products, raw materials, in-process materials, release test samples or stability samples, packaging materials, quantitative assays on samples, and/or finished products from manufacturing, to ensure quality standards and compliance with company standards, customer and governmental regulatory requirements, and tolerance specifications for the chemical or physical property Competencies: Can train others with appropriate experience Works independently working with discretion and judgment Requires working knowledge or skills developed through formal training or experience Capabilities / Technical Skills: As per skills matrix per site process Qualifications / Trainings: GxP certification - Internal, based on the site and Job Specific training system Quality / work procedures trainings Education: (Expected level of Education, may be impacted by Technology / Site Complexity) High School diploma required 2+ years’ quality experience in pharmaceutical / biotech required Bachelors degree in applicable discipline (chemistry, pharmaceutical or biology) a plus Master's Degree is conditionary / a plus

How you’ll spend your day

Your experience and qualifications

Enjoy a more rewarding choice

Make a difference with Teva Pharmaceuticals

Reports To

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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. 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.