Quality Control Analyst at Teva Pharmaceutical Industries Ltd. - Israel

Kfar Saba, Center District, Israel -

Full Time

Start Date

Immediate

Expiry Date

04 Jul, 26

Salary

0.0

Posted On

05 Apr, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Microbiological testing, GMP compliance, Sterility testing, Bioburden testing, Endotoxin testing, Environmental monitoring, LIMS systems, Root cause analysis, CAPA implementation, Aseptic practices, Data documentation, Method validation, Analytical thinking, Microbial identification, Laboratory safety

Industry

Pharmaceutical Manufacturing

Description

We Are Teva  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 Perform microbiological testing of raw materials, in-process samples, and finished products in compliance with GMP and pharmacopeial standards (USP, EP, BP). Conduct sterility testing, bioburden testing, endotoxin testing (LAL), and microbial identification. Perform environmental monitoring in cleanrooms, including air, surface, equipment, and personnel monitoring. Accurately document test results, prepare reports, and review data in accordance with regulatory requirements. Investigate deviations (OOS / OOT), participate in root cause analysis, and support CAPA implementation. Operate and maintain microbiology laboratory equipment such as autoclaves, incubators, biological safety cabinets, and LIMS systems. Participate in method validations, method transfers, and qualification of equipment and processes. Ensure compliance with laboratory safety, aseptic practices, and GMP procedures. Collaborate with Production, Quality Assurance, Your experience and qualifications B.Sc. in Microbiology / Biology / Biotechnology / Life Sciences – required. Hands-on experience in a microbiology laboratory, preferably in the pharmaceutical or medical device industry. Knowledge of GMP regulations and microbiological quality standards. Experience with sterility, bioburden, endotoxin (LAL) testing and microbial identification – advantage. Experience working in cleanroom environments and environmental monitoring – advantage. Familiarity with microbiology lab equipment (autoclaves, incubators, biological safety cabinets) and LIMS systems. Good English level – reading and writing SOPs and reports. High accuracy, analytical thinking, ability to work independently and as part of a team. Enjoy a more rewarding choice B.Sc. in Microbiology / Biology / Biotechnology / Life Sciences – required. Hands-on experience in a microbiology laboratory, preferably in the pharmaceutical or medical device industry. Knowledge of GMP regulations and microbiological quality standards. Experience with sterility, bioburden, endotoxin (LAL) testing and microbial identification – advantage. Experience working in cleanroom environments and environmental monitoring – advantage. Familiarity with microbiology lab equipment (autoclaves, incubators, biological safety cabinets) and LIMS systems. Good English level – reading and writing SOPs and reports. High accuracy, analytical thinking, ability to work independently and as part of a team. 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 Sr 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

Perform microbiological testing of raw materials and finished products while ensuring compliance with GMP and pharmacopeial standards. Manage environmental monitoring in cleanrooms and investigate deviations to support quality assurance processes.