Thank you for your interest in career opportunities at NeuroDerm.
Here are our current job openings.
We look forward to hearing from you.
Qualified candidates may submit their resume to [email protected]
Design Verification Engineer
Department: Device
Location: Rehovot, Israel
We are looking for a Design Verification Engineer.
Job Description:
- Interface with R&D and System Engineering to ensure requirements are received and defined to allow testability.
- Create verification protocols and reports .
- Lead testing campaigns by driving execution.
- Perform statistical analysis on collected data and present results.
- Define high level requirements for software tools, fixtures and equipment required to execute the test method.
- Document out of specs and deviation, analyze data and run initial failure analysis investigations with hand-off to System Engineering.
Job Requirements:
- Bachelor’s Degree in an engineering discipline.
- At least 1 year of experience in the Medical device industry .
- Experience in multidisciplinary project management – an advantage.
- Experience with R&D and design verification teams – an advantage.
- Fluent English- verbal and writing.
Medical Director
Department: Clinical Development
Location: Rehovot, Israel
We are looking for a Medical Director to provide medical and scientific expertise into the planning and execution of medical activities.
Job Description:
- Provide clinical input on pathophysiology, diagnosis, existing and emerging treatment options and unmet medical needs to inform key medical and business decisions
- Contribute to the clinical development plan of the products, from early stage of clinical development to preparation and submission of the Registration Dossier.
- Develop, review and approve clinical protocols, CSR, and other study documents in collaboration with study team.
- Interact with clinical pharmacology, safety, clinical operations, regulatory, device teams and other team members.
- Maintain appropriate strategic partnerships with centers of excellence and KOLs in areas of scientific interest.
- Plan and develop content for advisory board meetings with KOLs and medical symposiums.
- Provide on-going medical expertise and support to the Medical Affairs.
- Provide input and review scientific publications.
- Provide medical support within the company, including developing and delivering training curriculum and content.
- Serve as a medical representative to project-based cross-functional teams.
Job Requirements:
- M.D with work experience in clinical drug development.
- Minimum of 10 years of experience in the pharmaceutical industry, including previous experience in interactions with Regulatory Authorities.
- Preferably- experience in CNS and\or in drug-device product.
- Previous experience in submission (or preparation for submission) of CTD to FDA and/or EMA.
Associate Director, North America (NA)
Department: Clinical Development
Location: USA
We are looking for an Associate Director for the Clinical Development department, to oversee all studies activities and ongoing operations in NA.
Major duties and responsibilities:
- Support clinical trials operations at the region.
- Take part in global team meetings as the regional representative.
- Provide sponsor oversight at the region.
- Establish active network and communicates with CRO’s, vendors and supporting functions and site’s personnel within the region.
- Ensure compliance with Quality standards (SOP’s, GCP,GMP etc.).
- Take initiatives in anticipating and eliminating potential barriers throughout the daily work.
- Supervise recruitment at the region in partnership with the relevant global function.
- Mentor and oversee performance of sub-contractors.
Education and Knowledge Requirements:
- Experience as Clinical Trial Manager, including global phase 3 drug study management.
- Experience with medical devices or drug-device combination products.
- Monitoring experience.
- Direct management experience -preferred.
- Clinical trial operations experience across therapeutic areas preferred (e.g. clinical pharmaceuticals, CNS, Parkinson’s disease)
NDA/MAA Submission Lead
Department: RA
Location: Rehovot, Israel
We are looking for an experienced NDA/MAA Submission Lead.
Job Description
Responsibility for preparation and submission of branded drug-device combination in EU and US regulatory agencies:
- Establish and maintain infrastructure for file preperation and submission
- Leading the cross functional NDA/MAA project team
- Manage inovlved consultants and subcontractors, as needed
- Facilitate interdisciplinary agreement on file submission content
- Gap analysis to ensure quality submission and compliance with regulatory requirements /commitments to regulatory authorities
- Overview and integration of submission content
- Track, interpret and advise on applicable US and European regulations, guidelines, procedures and policies
Job requirements:
- Global regulatory experience and current knowledge of FDA Guidelines – A must
- Experience in global pharma
- Proven Project management capabilities
- Leadership without authority
- Excellent interpersonal relations
Experience with drug-device combination product/s – an advantage
System Engineer
Department: Device
Location: Rehovot, Israel
We are looking for an experienced System Engineer for developing new medical device in the drug delivery field (combination product).
Job Description
- Determine and write product and user requirements for medical device
- Coordinate technical functions though out the design process for system level behavior
- Translate requirements into designs that combine hardware, software and mechanics
- Write test protocols to verify requirements have been met
- Test sub-systems and system-level software
- Conduct risk analyses to ensure safe design
- Provide Input to automated testing tools
- Document procedures and results within the requirements of a medical device quality management system
Job requirements
Bachelor’s Degree in an engineering discipline And At least 5 years of system engineering experience in medical device industry. Product development lifecycle knowledge is required. Understanding of Medical Device design control. process. Ability to Work well with other engineers in a collaborative, and to work independently. fast-paced goal-driven environment. High level English and good documentation skills. Proficient in analytical skills, using tools to perform simulations. Willing to travel between local sites and abroad