Debiopharm Jobs Feed

IT Network Specialist

2012-05-02T13:21:35+00:00

Debiopharm Group est un groupe pharmaceutique global, basé en Suisse, qui se concentre sur le développement de médicaments innovants ciblant des besoins médicaux non satisfaits, principalement en oncologie. Debiopharm Group finance de façon indépendante l'ensemble de ses activités, et dispose d’une expertise dans tous les domaines relatifs au développement des médicaments, comprenant les essais précliniques, les essais cliniques, la synthèse des substances actives, les travaux de formulation et la fabrication de médicaments jusqu’au stade de l’enregistrement auprès des autorités de santé en vue d’une mise sur le marché.
Pour renforcer son service IT, Debiopharm SA à Lausanne recherche un(e)

IT NETWORK SPECIALIST

Vous êtes rattaché(e) au Directeur du département IT des sociétés de Debiopharm Group et vous faites partie d’une équipe créative et multidisciplinaire de huit personnes ; vous avez des interactions avec l’ensemble des collaborateurs de la société.

Vos activités:

Collaborer au quotidien au « Help Desk » informatique et bureautique de la société,
Fournir de l’aide et apporter des solutions aux utilisateurs pour tous les problèmes relatifs aux logiciels standards,
Participer à l’installation et à la maintenance des serveurs de l’entreprise, ainsi qu’au réglage et à la maintenance des éléments du réseau,
Participer à la mise en production, l’exploitation et l’évolution de logiciels dédiés,
Participer à la configuration, à l’installation et la maintenance des postes de travail des utilisateurs, ainsi qu’à l’installation d’accessoires, de périphériques informatiques et bureautiques, et également de périphériques d’impression,
Appliquer et faire respecter les procédures et standards de sécurité & qualité IT,
Recueillir et analyser les idées et besoins exprimés par les collaborateurs et services de l’entreprise,
Participer à la veille technologique IT.

Votre profil :

Vous possédez une bonne expérience professionnelle dans la configuration, le dépannage et la réparation d’appareils fixes ou portables (Windows, Apple iOS/OSX, etc…),
Vous avez une connaissance approfondie des principaux logiciels bureautiques (MS Office, MS Project, mise en pages, traitement d’images, vidéo, MS Visio, etc…),
Vous savez installer, configurer et maintenir des serveurs d’entreprise (Windows, UNIX, Linux, …) ainsi que des éléments actifs d’un réseau informatique (routeurs, switchs, firewalls),
Vous êtes à l’aise en LDAP, AD, VNP, SNMP, SSH, VNC et Telnet,
Vous avez l’habitude des procédures de sécurité informatique,
Vous souhaitez travailler dans un environnement « Help Desk » et avez démontré un esprit collaboratif dans vos expériences précédentes,
Vous pouvez intervenir, en cas de nécessité, les jours fériés et week ends,
De nature curieuse, méthodique et soucieuse du détail vous possédez également un très bon sens du contact et détenez un esprit orienté « client »,
Vous avez de bonnes connaissances en anglais,
Tout talent en programmation est le bienvenu (C/C++, PHP, HTML, SQL, Java, …)

Debiopharm vous offre :

Un environnement international et très dynamique, l'opportunité de rejoindre une entreprise à succès, à la pointe de l'évolution scientifique. La possibilité d’apporter une contribution à une société dans laquelle l'innovation, le sens des responsabilités et l’expertise de ses collaborateurs sont les fondements de son succès.

Si vous correspondez à ce profil, merci d’envoyer votre dossier par le biais du formulaire en ligne.

Pour plus d'informations sur nos activités: www.debiopharm.com

IT Systems Engineer

2012-04-27T16:12:53+00:00

IT Systems Engineer

Vous êtes rattaché(e) au Directeur du département IT des sociétés de Debiopharm Group et vous faites partie d’une équipe créative et multidisciplinaire de huit personnes; de plus, vous contribuez à un nombre important de projets intéressants au sein d’une organisation matricielle.

Votre mission:

Garantir l’intégrité, la disponibilité et les performances du système d’information,
Assurer la mise en production, l’exploitation et l’évolution de logiciels dédiés,
Rédiger des protocoles de qualification et participer à la validation de systèmes GMP (Good Manufacturing Practices),
Prendre en charge l’analyse et la solution des problèmes relatifs aux systèmes d’information et l’infrastructure IT,
Diriger ou participer aux équipes projets pour les choix et l’individualisation de solutions IT dédiées,
Appliquer et faire respecter les procédures et standards de sécurité & qualité IT et contribuer à leur évolution,
Participer à la veille technologique pour la recherche de nouvelles solutions et techniques IT,
Coordonner leurs activités et encadrer ponctuellement des prestataires de services,
Participer à la gestion courante et l’évolution des systèmes informatiques, du réseau et des connexions externes.

Votre profil :

Vous possédez une solide expérience en gestion de projets IT,
Vous avez une connaissance approfondie des protocoles, services et matériels réseau (TCP/IP, SNMP, SSL, VPN, SSH, VNC, Telnet, LDAP, …) des systèmes d’exploitation (Unix BSD, Solaris, Linux, Windows, …) et des bases de données (Oracle, MS SQL, …),
Vous êtes à l’aise en programmation (C/C++, PHP, HTML, SQL, Java, Javascript, …),
Vous possédez des compétences et de l’expérience dans les procédures de sécurité informatique,
Vous êtes à l’aise avec les outils d’administration, d’audit et d’analyse des systèmes et savez rédiger des notes techniques, des procédures et des supports de formation,
Vous avez le sens de la communication et possédez des aptitudes aux relations interpersonnelles qui vous permettent de comprendre les besoins des utilisateurs et de les traduire en solutions,
Vous savez hiérarchiser les priorités et gérer des situations d’urgence, qui peuvent requérir une intervention en week-end ou jour férié dans l’entreprise,
Vous aimez travailler en équipe et avez démontré un esprit collaboratif dans vos expériences précédentes,
Vous pratiquez aisément un anglais courant (oral et écrit).

Debiopharm vous offre :

Si vous correspondez à ce profil, merci d’envoyer votre dossier par le biais du formulaire en ligne.

Pour plus d'informations sur nos activités: www.debiopharm.com

“Associate Director” - Internal Medicine

2012-04-25T07:20:22+00:00

Debiopharm Group™ (Debiopharm) is a Swiss-based biopharmaceutical group of
companies with a focus on the development of prescription drugs that target unmet medical needs. Along with its unique business model, the success of Debiopharm is also based on its high level of expertise and talented people in various areas such as pre-clinical and clinical development, drug manufacturing, drug delivery, formulation, and regulatory affairs.

In order to reinforce our Research & Evaluation Department at our headquarters in Lausanne, we are looking for a specialist as

“Associate Director” - Internal Medicine

To play a key role in the evaluation of new candidate programs.

Your tasks:

Explore, with the other members of the team, the full potential of new drug candidates based on available scientific data for the purpose of in-licensing new projects
Organise and/or participate in the evaluation and due diligence processes of such programmes
Provide clear scientific recommendations to corporate Management concerning possible in-licensing contracts of new drug candidates
Elaborate clinical development plans for the programmes to be in-licensed
Collaborate closely with other departments within Debiopharm in order to facilitate the implementation of the R&D plans of newly in-licensed programmes
Maintain an international network of experts and opinion leaders and closely follow recent developments in internal medicine and oncology

Your profile:

You are a MD with a solid experience in Internal Medicine and Oncology
You have a strong track record in pre-clinical and clinical evaluation of drugs within the pharmaceutical or biotech industry
You are able to maintain the 'big picture' of your activity and use your creativity and scientific curiosity to explore the full potential of new molecules
You are able to maintain in-depth discussions with a team of high-level scientific experts
You accept challenge and are able to think 'out of the box'
You are completely fluent in English and French
You are willing to travel

Debiopharm can offer you :

An international and highly dynamic environment
The opportunity to join a successful company, at the forefront of the most advanced scientific developments in the industry
The possibility to be in a company in which innovation, people and entrepreneurship are the fundamentals of its success.

If you fit this profile please send your application using this form.

For more information : www.debiopharm.com

Alliance and Licensing Manager

2012-04-19T14:33:35+00:00

Debiopharm Group™ (Debiopharm) is a Swiss-based biopharmaceutical group of companies with a focus on the development of prescription drugs that target unmet medical needs. Along with its unique business model, the success of Debiopharm is also based on its high level of expertise and talented people in various areas such as pre-clinical and clinical development, drug manufacturing, drug delivery, formulation, and regulatory affairs.

For our Business Development & Licensing Department based at our headquarters in Lausanne, we are looking for an

Alliance and Licensing Manager

Who will report to the Director, Business Development and Licensing.

Your tasks:

Manage the alliance relationship with partners
Ensure internally the efficient communication and the collaboration with partners
Support the Research & Evaluation team in the identification of potential partners / projects of interest and perform commercial therapeutic area target screening
Coordinate internal commercial due-diligence to support the scientific evaluations on potential licensing candidates, summarising the rationale and findings in succinct written reports
Coordinate targeted competitive intelligence initiatives with the Business Intelligence functions. Coordinate financial /valuation analyses on potential business development transactions
Coordinate evaluation and support negotiation activities with potential partner companies;
Prepare and deliver presentations to senior management and to potential partner companies.

Your profile:

Life Sciences Degree
Minimum 3-5 years experience in a Business Development & Licensing function in the pharmaceutical or biotechnology industry
Prior experience and successful track record in acquisitions or licensing
Strong financial modeling and valuation skills, understands standard valuation methodologies
Ability to manage internal scientific, marketing and financial analyses
Ability to coordinate evaluation and negotiation procedures with potential partner companies
Proven ability to work with others to develop an effective business development team
Proactive and autonomous personality, able to adapt to a rapidly changing environment
Ability to work under pressure, with a good capacity to determine work priorities;
Languages: English and French
Travel: approx. 20%

Debiopharm can offer you :

An international and highly dynamic environment
The opportunity to join a successful company, at the forefront of the most advanced scientific developments in the industry
The possibility to be in a company in which innovation, people and entrepreneurship are the fundamentals of its success.

If you fit this profile please send your application using this form.

For more information : www.debiopharm.com

Laborantin(e) en chimie

2012-04-10T14:20:38+00:00

Debiopharm Group™ est une entreprise de développement et de production de produits
pharmaceutiques innovants, leader mondial dans son champ d’activité, nous cherchons pour consolider le secteur Contrôle Qualité Chimie de notre société Debio RP à Martigny un(e) :

Laborantin(e) en chimie

Votre mission :

Exécuter les analyses chimiques de routine du laboratoire (HPLC, tailles de particules, teneurs en eau, viscosité inhérente, pH, CCM, …) qui concernent le contrôle physicochimique des matières premières, du matériel de conditionnement, des produits intermédiaires, des produits finis, des échantillons prélevés sur les systèmes d’eau et des produits en étude de stabilité.

Votre profil :

CFC de laborantin(e) en chimie ou équivalent.
Expérience dans un service de contrôle qualité chimie soumis aux BPF.
Bonne connaissance des HPLC Agilent (Chemstation) et du logiciel Empower.
Esprit d’équipe, sens des responsabilités, rigueur, minutie et polyvalence.
Bonne maîtrise des outils informatiques.

Les personnes intéressées sont priées d’adresser une offre par e-mail par le biais du formulaire en ligne ou à l’adresse suivante :

DEBIO RECHERCHE PHARMACEUTIQUE S.A.
Service du personnel
Route du Levant 146/C.P. 368
CH - 1920 MARTIGNY

Medical Director

2012-04-01T23:00:00+00:00

Debiopharm Group™ (Debiopharm) is a Swiss-based biopharmaceutical group of companies with a focus on the development of prescription drugs that target unmet medical needs. Along with its unique business model, the success of Debiopharm is also based on its high level of expertise and talented people in various areas such as pre-clinical and clinical development, drug manufacturing, drug delivery, formulation, and regulatory affairs.

In order to reinforce our Medical Affairs Department we are searching for a talented and experienced expert to be based at our headquarters in Lausanne, Switzerland as :

Medical Director

You have a key leading role in our clinical development

Reporting to the Vice President Medical Affairs, you bring a major contribution to the strategy and you lead the operational plan related to the clinical trials of our new products in oncology.

Your main responsibilities and tasks :

Jointly with the experts in our company and our head of the department, you establish the most appropriate strategy for a successful clinical development of the products which will be assigned to you;
You validate the operational frame related to the clinical trials and work closely with the other services and departments mainly with the Clinical Operations and Project Management departments, as well as with internal and external experts, and key actors involved in the clinical trials, to ensure an optimal and successful development plan;
As an expert, you have the responsibility to be up to date with regard to the state-of-the art scientific and medical information; to participate in the conception of documents and papers announcing the results of the clinical studies; to develop and maintain strong relations with international experts and opinion leaders; to support, with your expertise, the licensing-out process with the collaboration of the VP Medical Affairs and the Business Development team.

Your profile :

You are Medical Doctor, expert in oncology, with a solid experience in the clinical development in the pharmaceutical industry, and an experience in both the strategy and the coordination of clinical operational activities.
You are therefore able to combine operational and project management skills with strategic and global thinking;
Team player, with strong interpersonal and leadership skills, you know how to work and collaborate efficiently in a team and in a matrix organisation, as well as develop efficient relations with Key Opinion Leaders and investigators;
You are rigorous, tenacious but pragmatic and solution oriented; You have a high level of scientific curiosity and a creative thinking;
You master English, French and are willing to travel.

Debiopharm offers you :
An international and highly dynamic environment; the opportunity to join a successful company, at the forefront of the most advanced scientific developments in the industry; the possibility to be in a company in which Innovation, People and Entrepreneurship are the fundamentals of its success.

If you fit this profile please send your application using this form.

For more information : www.debiopharm.com

Clinical Data Manager

2012-02-02T15:31:34+00:00

Debiopharm Group™ (Debiopharm) is a Swiss-based biopharmaceutical group of companies with a focus on the development of prescription drugs that target unmet medical needs. Along with its unique business model, the success of Debiopharm is also based on its high level of expertise and talented people in various areas such as pre-clinical and clinical trials, manufacturing, drug delivery, formulation, and regulatory affairs. In order to enhance and develop our Clinical Operations Department in Lausanne, we are looking for our new:

Clinical Data Manager

With a solid experience in Data Management

Reporting to the Director, Biostatistics and Data Management, you are accountable for all Data Management activities of clinical trials, in order to ensure completeness, accuracy and consistency of the data delivered on-time. You are a key member of the clinical project team. You are responsible for the set-up, maintenance, control, cleaning and validation of clinical study databases, in compliance with SOPs and regulatory agencies guidelines, in close cooperation with clinical trial managers.

Your main responsibilities and tasks :

Prepare clinical trials databases: approve CRF design; set-up e-CRFs; test entry screens and databases; parameterise randomisation.
Prepare data management plans and users guidelines, and train e-CRFs users.
Maintain clinical trial data accuracy: program edit checks, issue queries, manage resolutions and proceed to automatic coding.
Lock, transfer and archive databases.
Ensure adherence to regulations, GCPs, SOPs and working instructions.
Supervise data management tasks when outsourced.

Your profile :

Scientific or technical education background, ideally university level.
Minimum 5 years of experience in clinical trials data management, with proficiency in database programming.
Experience in all clinical data management activities, from study initiation to database lock.
Very good working knowledge of at least one clinical trial Electronic Data Capture database application.
Experience in Clinsight and/or SAS programming will be an advantage.
Good command of spoken and written English and French.
Autonomous, able to work independently.
Team player.
Able to manage stress and pressure.

Debiopharm can offer you :

An international and highly dynamic environment; the opportunity to join a successful company, at the forefront of the most advanced scientific developments in the industry; the possibility to be in a company in which Innovation, People and Entrepreneurship are the fundamentals of its success.

If you fit this profile please send your application using this form.

For more information : www.debiopharm.com