AS&T Project Leader - Quality Analyst at Teva Pharmaceutical Industries Ltd. - Israel

Kfar Saba, Center District, Israel -

Full Time

Start Date

Immediate

Expiry Date

23 Aug, 26

Salary

0.0

Posted On

25 May, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Analytical Lifecycle Management, cGMP Compliance, Method Validation, Technology Transfer, CAPA Implementation, Root Cause Analysis, LIMS, Pharmacopeial Requirements, Regulatory Affairs, Change Control, Deviation Investigations, Analytical Documentation, Quality Control, Supplier Qualification, Project Leadership, Cross-functional Collaboration

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 role sits within Analytical Science & Technology (AS&T) and plays a key part in ensuring robust, compliant, and sustainable analytical control across product lifecycles.As an AS&T Project Leader – Quality Analyst, you will lead and oversee analytical activities supporting technology transfers, post‑marketing changes, supplier qualification, and regulatory commitments, acting as a critical interface between QC, R&D, Quality, and Regulatory Affairs. The role offers broad exposure to global projects, complex analytical problem‑solving, and decision‑making with direct quality and regulatory impact, within a collaborative and values‑driven organization.How You’ll Spend Your Day Lead and support AS&T projects related to analytical lifecycle management, including post‑marketing changes, method updates, and site or technology transfers Implement, maintain, and continuously improve analytical SOPs in compliance with cGMP and global quality standards Ensure analytical methods and specifications are compliant with current pharmacopeial and regulatory requirements Coordinate and manage updates to analytical methods and specifications in collaboration with Regulatory Affairs / laboratory requirements Review, approve, and manage analytical documentation, including protocols, reports, deviations, and change controls Lead and document deviation investigations, root cause analysis, and CAPA implementation related to analytical activities Approve analytical methods, method validations, technology transfer and site transfer protocols and reports Review and approve finished product specifications, including post‑marketing and lifecycle updates Lead and support analytical method transfers between R&D, QC, and global QC laboratories Ensure analytical testing monographs are accurately defined, maintained, and governed within the LIMS system Provide analytical expertise for evaluation and qualification of alternative and post‑marketing suppliers Support Regulatory Affairs in preparation of submission dossiers, variations, and regulatory response letters Participate and support investigations, ensuring appropriate analytical assessments and corrective actions Support and participate in QC audits, regulatory inspections, and self‑inspections, including follow‑up on assigned actions Your Skills and Experience B.Sc. in Chemistry or another relevant scientific discipline (M.Sc. – advantage) Solid understanding of analytical methodologies, specifications, and validation principles Demonstrated experience working in a cGMP-regulated pharmaceutical environment Hands‑on experience with deviations, CAPAs, change controls, and analytical documentation Experience supporting or leading technology transfers and post‑marketing activities Familiarity with pharmacopeial requirements (USP, Ph. Eur., BP) and regulatory expectations Strong communication skills and ability to work effectively across global and cross‑functional teams 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

Lead and oversee analytical activities for technology transfers, post-marketing changes, and regulatory commitments. Act as a critical interface between QC, R&D, Quality, and Regulatory Affairs to ensure compliant analytical control across product lifecycles.