Appointed Pharmacist Date: Jan 17, 2026 Location: Shoham, Israel, 0000000 Company: Teva Pharmaceuticals Job Id: 65091 **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. **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?** 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 (https://performancemanager.successfactors.eu/sf/careers/jobsearch?bplte\_company=1080030P) 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. EOE including disability/veteran