Quality Analyst at Teva Pharmaceutical Industries Ltd. - Israel

Kfar Saba, Center District, Israel -

Full Time

Start Date

Immediate

Expiry Date

01 Aug, 26

Salary

0.0

Posted On

03 May, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

SOP implementation, cGMP compliance, Analytical methods, Pharmacopeias, Regulatory affairs, CAPA, Analytical documentation, Technology transfer, LIMS, Analytical expertise, Complaint investigations, QC audits, Self-inspections, Chemistry

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.Our Team, Your Impact This section is where we attract the attention of potential candidates and sell the role. How has the role come about? What makes it appealing? What are the key responsibilities? How is the role better with Teva than with another company? Wherever possible, we should bring through the essence of our EVP pillars, i.e., we care, we’re in it together, and we make work fulfilling.How You’ll Spend Your Day Implement and maintain SOPs in compliance with cGMP requirements Ensure analytical methods and specifications comply with current pharmacopeias Update analytical methods/specifications in coordination with Regulatory Affairs Investigate, document, and report deviations; lead CAPA activities Manage, prepare, review, and approve analytical documentation Approve analytical methods, technology transfer and site transfer protocols/reports Approve post-marketing finished product specifications Lead and support analytical method transfers between QC, R&D, and global QC labs Ensure testing monographs are defined and maintained in the LIMS system Provide analytical expertise for alternative and post-marketing suppliers Support Regulatory Affairs with submission dossiers and response letters Participate in complaint investigations and implement corrective actions Support and participate in QC audits and self-inspections, ensuring compliance and follow-up actions Your Skills and Experience B.Sc. (preferably in chemistry or another scientific field) Training in cGMP 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 way. Reports To Section Manager, Analytical Science and Technology Already Working @TEVA? Make sure to apply through our internal career site on Twist—your one-stop shop for career developmentTeva’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 Quality Analyst will implement and maintain SOPs in compliance with cGMP requirements and manage analytical documentation. They will also lead analytical method transfers and support regulatory affairs with submission dossiers and complaint investigations.