Mgr Regulatory Affairs

Date: Nov 20, 2025

Location:

Shoham, Israel, 0000000

Company: Teva Pharmaceuticals

Job Id: 65091

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.

The opportunity

We are looking for a highly skilled Appointed Pharmacist to join a leading global pharmaceutical company in a key regulatory position with direct responsibility for communication with the Israeli Ministry of Health. This role requires a seasoned professional with hands-on regulatory experience, strong ownership, and the ability to work independently without additional regulatory training.

How you’ll spend your day

Serve as the primary point of contact with the Israeli Ministry of Health for all aspects of dossier registration and lifecycle management
Prepare and submit new drug registration applications (generic and innovative)
Manage submissions for renewals and variations
Review, prepare, and approve PILs and PPIs
Review, prepare, and approve packaging materials
Maintain full regulatory compliance throughout the product lifecycle
Collaborate closely with internal cross-functional teams, including Quality Assurance (QA), Pharmacovigilance (PV), Supply Chain (SC), and global regulatory counterparts
Support and lead regulatory projects and improvements across the organization

Your experience and qualifications

B.Pharm degree – mandatory
Experience as an Appointed Pharmacist – mandatory
Proven experience in regulatory affairs, including new submissions, renewals, variations, labeling, and packaging components
Strong understanding of generic and innovative products
High level of accuracy, attention to detail, and excellent organizational skills
Stong English communication skills (written and verbal)
Ability to work independently, manage multiple priorities, and meet deadlines
Strong ability to work with digital systems and regulatory platforms
Excellent interpersonal skills and ability to collaborate with multiple stakeholders locally and globally

Make a difference with Teva Pharmaceuticals

Reports To

Senior Manager Regulatory Affairs

Already Working @TEVA?

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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.