דרושים בתחום ניהול פרוייקטים מדעיים

· Responsible for regulatory submissions, approvals and compliance for worldwide market expansions and renewals
· Full understanding of regulatory file template and ability to maintain and update the quality part (CMC sections) in regulatory file
· Evaluate change requests and regulatory impact and establish the appropriate strategy for the projects at BTG
· Ability to write variations/ supplements and to drive approvals globally
· Maintain collaborative work with regulatory teams within BTG and globally
· Provide regulatory support to development activities and drive clinical trial application under development projects
· Review and approve Protocols, Reports and Validation documents
· Responsible for continuously acquiring new knowledge and finding innovative solutions to regulatory challenges and issues
· Provide regulatory CMC intelligence to cross-functional teams
· Demonstration of full understanding of regulatory requirements for the biopharma industry (drugs, medical devices, biologicals) and demonstrate regulatory CMC expertise

· Academic degree in science (MSc or PhD) in any area of biology, life sciences or molecular biology - must
· Hebrew and English at mother tongue level, with proven abilities in writing and editing of submission documents – must.
· At least 5 years experience in the pharma industry, or 3 years in regulatory affairs and product registration of pharma products – must
· Excellent oral and written communication skills, with ability to work as part of a team- must
· Scientific understanding of CMC requirements and submission content concerning product quality- an advantage
· Ability to simultaneously manage and drive multiple projects to achieve new registration and support change variations - must
· Ability to work independently, work under pressure and to meet changing deadlines- must
· Logical thinking, assertiveness, creativity and flexibility - must
· Computer literacy, including experience with Microsoft Office Word, Excel and Power Point.
· Understanding of GMP and Quality System requirements – an advantage
· Computer literacy, including experience with Microsoft Office Word, Excel and Power Point.
· Knowledge of and experience with US and EU regulatory requirements for the biopharma industry (drugs, medical devices, biologicals) - an advantage.