Quality Regulatory Manager

Regulatory Affairs Manager (Appointed Pharmacist not a mandatory)In this role, you will take ownership of regulatory submissions and approvals in Israel, managing the end-to-end registration process for innovative medicines, generics, and established molecules. You will serve as the key contact with the Ministry of Health and other regulatory bodies, while...

Quality Assurance Manager – Leading Pharmaceutical CompanyA leading pharmaceutical company is seeking an experiencedQuality Assurance Managerto lead and manage quality operations at the production site.Key Responsibilities:Manage all quality systems at the production site in compliance with regulatory requirements (GMP, Ministry of Health, FDA, EMA).Lead...

hms, a leading strategic consulting firm in Israel, is looking for aProject Managerto lead a high-impact regulatory project for a governmental client.This is a meaningful opportunity to influence national-level decision-making processes and drive regulatory transformation.Hybrid work model– work from both client site and home.What will you do?Lead...

In this role, you will take ownership of regulatory submissions and approvals in Israel, managing the end-to-end registration process for innovative medicines, generics, and established molecules. You will serve as the key contact with the Ministry of Health and other regulatory bodies, while working closely with internal teams to drive projects forward.What...

Department:QualityLocation:EMEA-IsraelDescriptionAbout this opportunityIn this position, you will develop and execute regulatory strategy, work closely with R&D and Engineering departments to provide regulatory inputs relevant to product development and changes, write and submit submission packages to FDA, EU, and work closely with worldwide RA partnersKey...

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities...

Regulatory Affairs Specialist – Medical DevicesLocation:Yokneam Illit | Full-Time PositionA global medical device company is seeking a talented Regulatory Affairs Specialist to join its team and take part in managing regulatory processes for cutting-edge medical device solutions across international markets.Key Responsibilities:Manage product registration...

Responsibilities:Manage and control Quality Management System (QMS) processes in general and specifically risk management, design controls and transfer to production activities.Write, review and approve quality procedures and work instructions.Collaborate with cross-functional teams to ensure quality standards throughout the product lifecycle.Maintain a...

Eitan Medicalis a fast-growing global medical device company, developing and manufacturing innovative drug delivery and infusion solutions across the continuum of care- from the hospital to the home. We are looking for an excellentDesign Quality Engineerto join the QA product teamJob Description:As a Design Quality Engineer, you will be the focal point for...

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You'll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.A Day in the LifeIf you have experience in regulatory compliance and enjoy working with cutting-edge medical...