Jostein Grip Email and Phone Number

Responsibility for product development of medical device class III within the Company, in-line with SOPs and applicable regulations, as well as managing development of platform technology for aquaculture. Tasked with identifying new partners and exploring innovative business opportunities to expand the application of our oxygenation technology platform.Facilitate traction on projects in accordance with milestones and budget.Responsible for technical documentation for pre-clinical and clinical investigation.IP-management and supportCommunication and follow-up of Contract Development and Manufacturing Organization (CDMO) and Contract Research Organization (CRO)- pre-clinical and clinical.Responsible for product changes.Issue/approve product documentation and reports.Reporting to public research funding organizations.

Development of new products for genetic analysis of diseases.Secure co-operation with company resources in production, lab, QA and external companies.Manage projects and milestones for new products.Secure appropriate risk management of new products.Actively seek patentable matters during product development.Secure compliance to regulatory framework during product development and implementation.Co-ordinate establishment of quality documents for new products.

Development of new hydrogel and nanofiber dressing products for the "hard-to-heal" wound segment (medical device), with bio-active/immune modulating API.Manage projects and overall work plans for new products.Secure compliance to regulatory framework during product development.Secure appropriate risk management of new products.Aid in and co-ordinate establishment of quality documents for new products.Secure co-operation with company resources in production, lab and QA.Coordinate product development projects.Actively seek and support patentable matters during product development.

Designing and conducting membrane transporter interaction studies (e.g. drug-to-drug interaction).Evaluating the generated data.Writing expert reports in compliance with the regulatory agencies (FDA and EMA).Providing professional opinion and recommendations.Participating in assay development processes.Holding seminars on ADME/Tox.Client communication and client visits.

Commenting government hearings on behalf of union members.Gathering research articles for journal.

Monitoring health and welfare status of Atlantic salmon for 7 sea-based fish farms. Quality sampling (fat and astaxantine content) and sampling for histology. Project planing of new locations (land and sea-based).

Sampling organs and blood, registration of environmental parameters, infecting hosts (fish), testing samples specified by clients, bacteriology tests, practical follow-up of infection experiments.Part time while studying.