עדיין מחפשים עבודה במנועי חיפוש? הגיע הזמן להשתדרג!
במקום לעבור לבד על אלפי מודעות, Jobify מנתחת את קורות החיים שלך ומציגה לך רק משרות שבאמת מתאימות לך.
מעל 80,000 משרות • 4,000 חדשות ביום
חינם. בלי פרסומות. בלי אותיות קטנות.
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.
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
- This is a temporary position, serving as a maternity leave replacement for a period of approximately 6–9 months.
- 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.
Mgr Quality Control
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. 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.
Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, genetic information, marital status, sexual orientation, gender identity or expression, ancestry, national or ethnic origin, citizenship status, military status or status as a disabled or protected veteran, or any legally recognized status entitled to protection under applicable federal, state, or local laws.
במקום לעבור לבד על אלפי מודעות, Jobify מנתחת את קורות החיים שלך ומציגה לך רק משרות שבאמת מתאימות לך.
מעל 80,000 משרות • 4,000 חדשות ביום
חינם. בלי פרסומות. בלי אותיות קטנות.
שאלות ותשובות עבור משרת Quality Control Analyst (Temporary - Maternity Leave Replacement)
התפקיד כולל הכנת חומרים ותיאום תכנון לבדיקות מוצרים יומיות, קבלת ורישום דגימות, ביצוע בדיקות אנליטיות במעבדה (כולל HPLC, UV), סקירת ואימות רשומות מעבדה, ביצוע מחקרי יציבות ותמיכה בחקירות. מדובר בתפקיד זמני להחלפת חופשת לידה, לתקופה של כ-6–9 חודשים.
משרות נוספות מומלצות עבורך
-
Quality Control Analyst (Temporary - Maternity Leave Replacement)
-
כפר סבא
Teva Pharmaceuticals
-
-
QC Analyst
-
תל אביב - יפו
IFF
-
-
אנליטיקאי/ת למעבדת בקרת איכות ביולוגית
-
אור עקיבא
ביוואק מוצרים וטרינר
-
-
למטריקס (מרכז) דרוש/ה אנליסט/ית איכות - זמני
-
נס ציונה
צפון matrix
-
-
Quality Control Analyst
-
כפר סבא
Teva Pharmaceuticals
-
-
Quality Control Analyst
-
כפר סבא
Teva Pharmaceuticals
-