Careers

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