Pharmacist or PhD in scientific discipline - Minimum of 5 years of experience in the pharmaceutical industry - Minimum of 3 years of experience with Medical Affairs - Affinity with Sales & Marketing and Market Access - Good analytical capabilities - Excellent communication skills Are you
all relevant documents, tests, validations in order to meet project requirements, and are able to make choices and defend decision - Promotes Regulatory Affairs awareness throughout company - Continuous improvement on the field of RA - You will report to the Manager RA & QA
the Medical Devices department of the bigger company and their products are sold worldwide. ROLE DESCRIPTION You are proactively monitoring the latest legislation and regulations in in the field of Pharma and Medical Devices and regulations that are
on your current experience level. You will help set up the pivotal study in the EU and help identify and select study sites. You review clinical data and manage documentation and reports. There will be collaboration with the company's R&D team, QA and clinical affairs team. You are responsible for
Affairs is responsible for: - Be aware and stay informed of all relevant regulatory requirements. Actively monitoring developments in the field of regulatory in all relevant markets and advice the management by showing reports and action plans. - The complete product registration process. This includes
einem Medical Science Liaison Manager (MSL) zum nächstmöglichen Zeitpunkt. RESPONSIBILITIES - wissenschaftlicher Austausch mit KOLs - Kommunikation und Zusammenarbeit mit den Abteilungen Regulatory Affairs, Pharmacovigilance, F&E, etc. - Betreuung von klinischen Studien
new liquid products or changes to existing liquid products; - Ensures that all project documentation is delivered according to the applicable law and legislation for medical devices and pharmaceutical product; - Is also responsible for timely execution of the advice, review and approval tasks ...
Russia, Turkey Middle East REQUIREMENTS - 3-5 year of experience in Medical Devices - Knowledge of regulatory submissions - Knowledge of regulations outside of Europe - Flexible attitude - Good knowledge of both Dutch and English - Able to move for the duration of the
least 5 years of experience with Regulatory Affairs in an internationally operating food company. - Experience with project management is an asset. - Fluency in Dutch and English required, fluency in German and/or French is an asset. Are you interested and do want to apply for this role ...
main focus of this job is to maintain the life cycle management of OTC pharma products. In addition the manager is also involved in the development and registration of new products. RESPONSIBILITIES Manager you are responsible and involved in: - LCM of OTC pharma - Newly
Manager RESPONSIBILITIES - Management of the global submission process - compilation and review of regulatory documents - management of submissions with focus on Europe and other countries globally - support of regulatory activities of the companies other locations as
As a regulatory affairs manager you will be responsible for the regulatory strategy and global regulatory deliverables for the company. RESPONSIBILITIES - Provide guidance, direct and lead a team of regulatory professionals - Liaison relationships with regulatory
product improvement/development. Quality and development go hand in hand here and result into customer satisfaction. ROLE DESCRIPTION To ensure the developments and innovation reach the customer you as European Regulatory Affairs Manager will be in charge
SIRE Life Sciences® is the market leader in life science recruitment. We believe the recruitment market needs to gear up in technology and continues innovation. We like technology, in a life science market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced ...