Senior Scientist Biological Evaluation

Q-med / Biomedicinjobb / Uppsala
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Professionalism, innovation and simplicity are concepts that characterize Galderma. Galderma offers you an opportunity to work in a company with strong growth where opportunities for personal and professional growth are good.

At Galderma, more than 4,000 people are committed to delivering innovative medical solutions to meet the dermatological needs of people throughout their lifetime.

Just as the skin is a unique system within our body, we offer a unique and complete skin care portfolio ranging from prescription and self-medication treatments to aesthetic & corrective solutions. Located in Uppsala in Sweden, Q-Med AB is the global centre of excellence for Aesthetic & Corrective, with state-of-the-art research, development and manufacturing.

Our 400 employees in Uppsala are committed to leading brands such as Emervel® and Restylane® fillers, skinboosters and skincare, Azzalure and Pliaglis.
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We are now looking for a candidate that will work as pre clinical expert with responsibility for pre clinical investigations and safety assessments, both according to regulatory guidelines during development but also within our early research projects. The position is permanent and based in a group called Biological Evaluation within the Research department in Uppsala, a site with responsibilities for the Aesthetics & Corrective (A&C) products. The Research department in Uppsala is reporting to the Research Director in Sophia-Antipolis, France, and you will collaborate with colleagues at Galderma Scientific Division in France, the world's largest R&D center specialized in dermatology. The main focus for Biological Evaluation is to give scientific support on biological and preclinical questions within Research and Development projects, including defining and initiating preclinical program and compilation of files for registration for new products within the A&C business unit (fillers, toxin, injection devices) and ensure that we are working according to guidelines for medical devices. 
• Coordinating short term and long term pre clinical activities• Define strategies for pre clinical activities including toxicological and safety assessments• Ensure that requested studies are compliant with ethic and regulatory guidelines• Writing and reviewing scientific reports as well as regulatory documents within the field• Scientific support to marketing and medical affairs when requested• Participate in cross-site and cross-functional project and activities as pre clinical expert• Collaborate with colleagues from R&D in Sophia Antipolis as well as external contacts• Coordinating activities related to explorative biological evaluation of fillers and ensuring correct delivery of biological data to support projects needs and transitions 
• Advanced degree in a field relevant for Biological Evaluation of bio materials• At least 5 years of experience with pre clinical issues including strategic decisions, preferable both for medical devices and drugs • Leadership experience, as line manager is an advantage• Experience in regulatory frameworks for Medical Device and preferable also for drugs• Experience in toxicology, immunology or cell biology is an advantage• Highly motivated and able to work in teams as well as independently• High multi-tasking capacity


Arbetstider och omfattning
Full- time Contract


Så ansöker du
Sista dag att ansöka är 2013-11-30
For further information please contact Anne Helander Kenne , Head of  Research,
• 46 733871454. You register your CV and apply for the position at " shape="rect" target="_blank">Klicka på denna länk för att göra din ansökan . We would like to have your application by latest November 30, 2013.
Ansökan kan tyvärr inte göras via e-post.
Klicka på denna länk för att göra din ansökan

Sandra Mattsson


Seminariegatan 21
75228 Uppsala


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