Head of Labelling
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Hobson Prior are currently working with a world-wide aesthetics and neurotoxin organisation who are seeking a Head of Labelling to join them on a permanent basis in Frankfurt.
Responsible for ensuring all regulatory activities and optimising labelling processes.
Heading up the transposition of approved texts into national use and specialist information for medicinal products.
Ensure the conformity of advertising and scientific information with the appropriate authorisation.
Formulate and make recommendations on informative texts of medicinal products.
In charge of leading and creating the Labelling/Advertising team in the field of Global Regulatory Affairs.
Progress departmental goals and support the continuous development of your employees.
Complying with budgets, organization and processes.
Act as the information officer
Provide information to professionals and other relevant parties about the pharmaceutical quality, effectiveness and safety of medicinal products.
Testing and release of scientific information and promotional materials in accordance with HWG and Directive 2001/83 EC.
Preparation, modification and verification of the mandatory texts for advertising and drug entries in compendiums and databases.
Responsible for the introduction and optimization of transparent, efficient and synchronised processes in close cooperation and coordination with relevant functions and specialist departments as well as partners and external service providers.
Knowledgeable in the field of new approval and global approval business of pharmaceuticals and other product classes.
Extensive experience in regulatory life-cycle management and in the maintenance of international approvals.
Wide-ranging knowledge of the international regulatory framework (labelling), especially in Germany and the European Union.
Proficient at dealing with and interpreting admission and legal texts.
Excellent communication skills consisting of German and English both spoken and written, any other foreign languages are desirable.
Degree level educated in natural sciences in the field of pharmacy, biology or chemistry, supplemented by an approval as a pharmacist.
Several years of professional experience in the authorisation of medicinal products, their maintenance and in the field of product information texts/labelling in a leading role.
Meet the requirements of the Information Officer in accordance with AMG 74a.
If you are interested in learning more or applying to this exciting opportunity, please complete the form below and attach a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist, please request a call back at the top of this page.
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