Quality Control Analyst at Teva Pharmaceutical Industries Ltd. - Israel

Kfar Saba, Center District, Israel -

Full Time

Start Date

Immediate

Expiry Date

17 May, 26

Salary

0.0

Posted On

16 Feb, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Analytical Testing, HPLC, UV Spectroscopy, Laboratory Analysis, Record Review, GxP Compliance, Stability Studies, Instrument Maintenance, Calibration, SAP, Documentation, Attention to Detail, Organizational Skills, Teamwork, Procedure Following, Interpersonal Skills

Industry

Pharmaceutical Manufacturing

Description

Who we are We’re Teva, a leading innovative biopharmaceutical company, enabled by a world-class generics business. Whether it’s innovating in the fields of neuroscience and immunology or delivering high-quality medicine worldwide, we’re dedicated to addressing patients’ needs now and in the future. Here, you will be part of a high-performing, inclusive culture that values fresh thinking and collaboration. You'll have the room to grow, the flexibility to balance life with work, and the opportunity to better health worldwide, together.How you’ll spend your day Preparing materials and coordinating planning for daily product testing activities Receiving, logging, organizing, and disposing of samples according to procedures Performing analytical tests, including basic and intermediate laboratory analyses Conducting qualitative and quantitative testing using analytical instruments such as HPLC, UV, and other site‑specific technologies Reviewing, checking, and verifying laboratory records to ensure accuracy and compliance Inspecting and proofreading incoming printed literature and releasing it in SAP once approved Executing stability studies, including staging and placing samples in stability chambers Supporting investigations, documenting findings, and providing test results to relevant stakeholders Maintaining laboratory instruments, assisting in calibrations, and ensuring equipment readiness Collaborating with team members, supporting training activities, and contributing to a positive, professional lab environment Your experience and qualifications Bachelor’s degree in Chemistry, Biology, Pharmaceutical Sciences, or a related field preferred Previous experience in an analytical laboratory environment - a strong advantage Familiarity with analytical methods and laboratory workflows, including techniques such as HPLC, UV, and other routine analytical instruments. Understanding of GxP principles and experience working in a regulated environment - preferred.Ability to review, verify, and document laboratory results with high accuracy and attention to detail.Strong organizational skills and the ability to follow procedures and protocols meticulously. Good English skills for reading and writing SOPs, reports, and technical documentation. Strong interpersonal skills, team‑oriented mindset, and willingness to support and collaborate with colleagues. Ability to learn new methods and technologies, demonstrating curiosity, motivation, and ownership. High level of responsibility, precision, concentration, and the ability to work efficiently under varying workloads. How We’ll Take Care of You  At Teva, better health starts from within, and that includes you. From day one, you’ll be supported with benefits designed to help you thrive in and out of work. This includes generous annual leave, reward plans, flexible working schedules (dependent on role), access to tailored health support, and meaningful ways to give back to the community.  When it comes to your career, you’ll be encouraged to explore, evolve, and shape your path. Twist, our one-stop shop for career development platform, gives you access to a wide range of possibilities, from learning programs and short-term projects to opportunities for internal growth. Here, you’ll be part of a culture that empowers you to reach your goals and prioritize your wellbeing every step of the wayReports To Mgr Quality ControlAlready 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. 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.

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Responsibilities

The analyst will be responsible for preparing materials, coordinating daily product testing, performing qualitative and quantitative analytical tests using instruments like HPLC and UV, and reviewing laboratory records for accuracy and compliance. Key duties also involve executing stability studies, supporting investigations, and maintaining laboratory equipment readiness.