Medison Pharma ir globāls farmācijas uzņēmums, kas palīdz nodrošināt inovatīvu terapiju pieejamību pacientiem starptautiskajos tirgos. Tā starptautiskā komercializācijas platforma atbalsta jaunu ārstēšanas metožu ieviešanu un pieejamību dažādos reģionos, savukārt sadarbība ar farmācijas un biotehnoloģiju uzņēmumiem palīdz paplašināt zāļu pieejamību un uzlabot pacientu iespējas saņemt ārstēšanu visā pasaulē.
Regulatory Affairs Specialist – Israel (Hybrid)
Prepare and maintain pharmaceutical product registrations, renewals, variations, patient leaflets, and packaging. Coordinate regulatory work with Israel’s Ministry of Health and international partners.
Apraksts
- Compile registration dossiers and verify that their contents meet applicable requirements
- Write consumer leaflets
- Develop product packaging
- Manage regulatory changes, renewals, updates, and leaflet requirements
- Support activities across the pharmacy division
- Prepare submissions for products, renewals, variations, leaflets, and packaging
- Keep product regulatory dossiers current
- Liaise directly with Israel’s Ministry of Health and partners abroad
- Review regulatory materials and documents
Prasības
- Bachelor’s degree in pharmacy or a life science field such as chemistry or biology
- At least two years of Israeli regulatory affairs experience, including pharmaceutical product registrations, renewals, and variations
- Strong English skills
- Excellent Hebrew skills
- Proficiency with Microsoft Outlook, PowerPoint, Word, and Excel
- Strong attention to detail
- Ability to work under pressure
- Energetic and hardworking approach
- Trustworthy conduct