Regulatory Affairs Specialist works mostly with countries all over the world on the International registrations. This can be a person that is looking to step into the regulatory field, and wants to learn and work together with some of the brightest experts in the fields of regulatory, quality, development ...
responsible for releasing finished drug product lots while ensuring compliance with the requirements of the marketing authorization and good manufacturing practices. As a Specialist Plant QA, you provide guidance and direction to Production, Maintenance & Engineering and Quality staff regarding compliance
journey of growth!Role DescriptionThe Tech Transfer Specialist is responsible for assisting with the transfer of manufacturing processes and/or technology from R&D to the plant manufacturing plant. He/she participates in (1) designing manufacturing procedures for new or modified products, (2) planning ...
and Biotechnology organisation, based in Zuid-Holland Netherlands.The CompanyJanssen Infectious Diseases and Vaccines (formerly Crucell) is a biotech company that focuses on the development, production and marketing of vaccines, recombinant proteins and antibodies to prevent and combat infectious and
shipped to various countries worldwide.Every day more than 600 people in the Netherlands are working on supply chain processes, Engineering, marketing and sales of our medicines and clinical research into new medicines.We encourage our team members to have fulfilling and meaningful careers through
product lots while ensuring compliance with the requirements of the marketing authorization and good manufacturing practices. As a Specialist Plant QA, you provide guidance and direction to Production, Maintenance & Engineering and Quality staff regarding compliance with quality standards and
a wholly owned subsidiary of Johnson & Johnson.Role DescriptionWe are looking for a Regulatory Affairs Data Verification Specialist to coordinate and support data verification in the Marketing-Authorisation (MA) data tracking system in InSight. This role is critical to ensure the accuracy of EMEA data in
(outsourced) process development, characterization and validation activities • Responsible to ensuring close collaboration with the Fresh Frozen Plasma manufacturing specialist and ensuring alignment with project needs through Technical Integrator • Responsible as technical subject matter expert in case
Dechra richtlijnen. Dit in goede samenwerking met het regulatory affairs team, marketing, QA, productie afdelingen, externe producenten en farmacie. Daarnaast heb je een ondersteunende rol binnen het RA team voor diverse werkzaamheden. Je rapporteert aan de Senior Regulatory Affairs