Offres de stage et d'emploi

Offres de stage et d'emploi

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Voir les offres du pôle Industrie39


STAGE AFFAIRES REGLEMENTAIRES

Labatec - Genève, Suisse

Labatec Pharma : Société privée et implantée en Suisse, Labatec est une compagnie pharmaceutique qui possède plus de 50 ans d’expérience dans la production et mise sur le marché de produits pharmaceutiques de haute qualité. Labatec développe et commercialise des médicaments qui contribuent à améliorer la qualité de vie de patients du monde entier, en parfaite synergie avec les besoins des secteurs hospitalier et retail. Fabriqués en Europe et approuvés par Swissmedic, nos produits représentent une marque pharmaceutique européenne de confiance. Notre vaste portefeuille comprend des produits injectables et oraux à usage hospitalier ainsi que des produits de spécialités, ciblant de multiples domaines thérapeutiques dont les pathologies musculosquelettiques et la santé de la femme. Missions principales :  Au sein du département des affaires réglementaires, nous recherchons un stagiaire afin de soutenir nos activités quotidiennes, notamment de :  Préparation et soumission des dossiers réglementaires (nouvelles demandes d’AMM, variations, renouvellements…)  Elaboration et revue des textes de labelling  Revue du matériel promotionnel  Veille réglementaire Profil recherché :  Formation scientifique (Médecine, Pharmacie, Ecole d’ingénieur, Master scientifique …)  Rigoureux et organisé, désirant travailler en équipe  Langues : Français et Anglais courant. L’Allemand serait un vrai plus Stage d’une durée de 6 mois minimum. Poste à pourvoir dès que possible Localisé à Genève, Suisse Merci d’envoyer votre CV et lettre de motivation à travers du link suivant :  https://labatec.bamboohr.com/jobs/view.php?id=24

Publié le 2019-12-05 - Par Caroline GUERIN

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IFPMA Young Professionals Fellowship 2020-2021

IFPMA - Geneva, Switzerland

The IFPMA Young Professionals Fellowship is an opportunity for members of the International Pharmaceutical Students’ Federation (IPSF) to engage with IFPMA and its membership and be a credible voice in dialogue with the global health community. About IFPMA: IFPMA represents research-based pharmaceutical companies and national associations across the globe. The research-based pharmaceutical industry’s two million employees research, develop and provide medicines and vaccines that improve the lives of patients worldwide. Based in Geneva (Switzerland), IFPMA has official relations with the United Nations and brings the industry and broader health community together to foster innovation, promote resilient regulatory systems, uphold ethical practices, and advocate for sustainable health policies that meet the needs of patients globally. For more information, please visit http://www.ifpma.org/ The Fellowship: The Fellowship is a full-time, 12-month, compensated position in global health policy, with a particular focus on regulatory system strengthening. The Fellow will support the portfolio manager(s) on projects to promote policies, dialogue and initiatives that encourage regulatory reliance to improve access to medicines and vaccines globally as well as building capacity for the regulation of advanced innovative therapies. Activities may include the development of policy, educational, research and communication materials to strengthen the role of regulatory frameworks globally, with particular emphasis in Africa. The Fellow will also be involved in the preparation of key meetings, briefing documents and presentations on various topics in support of external engagement activities. A second angle of the fellowship will be to support the Ethics & Compliance portfolio lead, focused on the creation of strong ethical standards for all IFPMA members through the further development and implementation of a self-regulation framework (the IFPMA “Code of Practice”) in order to build trust among stakeholders and ultimately patients. Activities may include surveying member associations on KPIs around Code implementation, preparation of meetings, workshops, briefing documents and presentations, as well as support with the development of an online learning tool on the Code. The Fellow will liaise with other IFPMA Teams as necessary to complete the various projects. Location: IFPMA Office @Campus Biotech Building B2, Level 04 Chemin des Mines, 9 1211 Geneva, Switzerland Timing: Start Date: March 2020 End Date: March 2021 Candidate Profile: The Fellow should have the following skills/attributes: ● Excellent command of both written and spoken English. Knowledge of other languages, e.g. French or Spanish are an asset ● Good knowledge and interest in pharmaceutical policy and vaccine topics, and an understanding of international and multi-lateral organizations ● Good communication, research and presentation skills ● A hands-on approach and confidence to take on different projects at the same time with good organization skills ● Creativity and problem-solving skills Eligibility: IFPMA may accept applicants who meet all of the following conditions: ● 1) In possession of a valid Swiss Work Permit; or 2) Citizen of one of the following countries: Switzerland, European Union (EU), Argentina, Australia, Canada, Chile, Japan, Monaco, New Zealand, The Philippines, Russia, South Africa, Tunisia, Ukraine and United States of America (USA); ● Under 35 years of age in 2019. Applicants from Australia, New Zealand & Russia must be under 30 years of age in 2020. For more information, please visit here; ● Applicants who have completed their study (at a university or an equivalent institution leading to a formal qualification) by the time the Fellowship will take place; ● Applicants who are fluent in English; and ● Applicants who are not related to a staff member of IFPMA. Application Process: All current IPSF Members meeting the above requirements are eligible to apply. IFPMA will be responsible for the final selection of Applicant(s). Successful Applicant(s) undertaking a Fellowship will not be financially remunerated by IPSF. IFPMA will provide financial compensation for the duration of the Fellowship. The applicant(s) will be responsible for their own accommodation and travel expenses. As part of the application process, please submit: ● A Cover Letter in support of the application; ● A Curriculum Vitae (CV) in English; ● An example of previous written work completed as part of your studies to demonstrate your writing skills. Please submit electronic copies of your full application to Ms. Karima Bennara, IPSF Internship Coordinator 2019-2020 at internship@ipsf.org no later than Friday, 13 December 2019 23:59 GMT +0. Please use the subject line “IFPMA Young Professionals Fellowship”. Only PDF format of all applications will be accepted. IPSF will complete the 1st round selection process, and IFPMA will make the final selection. The results of the Fellowship will be announced by IPSF to all candidates. A successful candidate from Argentina, Australia, Canada, Chile, Japan, Monaco, New Zealand, Philippines, Russia, South Africa, Tunisia, Ukraine, USA will also need to comply with the procedures outlined by Switzerland’s State Secretariat for Migration (SEM). If you have any questions about the Fellowship, please do not hesitate to contact IPSF Internship Coordinator at internship@ipsf.org or IPSF Chairperson of Pharmacy Education at education@ipsf.org.

Publié le 2019-11-22 - Par Caroline GUERIN

Du 2020-03-02
Au 2021-03-01

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Next Generation Scientist Program by Novartis and University of Basel

Novartis - Bâle (Suisse)

The Next Generation Scientist Program by Novartis and University of Basel is an intensive internship program for talented and motivated research scientists from emerging countries. The 3 month program (1st June to 31st August 2020), hosted at the Novartis research site in Basel, Switzerland, is designed to foster both their scientific and professional development. Guided by Novartis mentors, the interns will work on a jointly-agreed upon scientific or clinical research project and also participate in a leadership development program designed to enhance their decision-making and communication skills.

Publié le 2019-10-21 - Par Caroline GUERIN

Du 2020-06-01
Au 2020-08-31

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IMP Placement - Portfolio Strategy Intern

Fresenius Kabi - Bad Homburg, Allemagne

[IMP Placement - Fresenius Kabi] EPSA offers now a new IMP Placement as a Portfolio Strategy Intern in Fresenius Kabi - Bad Homburg, Germany. ♦️Fresenius Kabi (preferably tagg them) is a global health care company that specializes in lifesaving medicines and technologies for infusion, transfusion and clinical nutrition. The company's products and services are used to help care for critically and chronically ill patients. With its corporate philosophy of “caring for life”, Fresenius Kabi is committed to putting essential medicines and technologies in the hands of people who help patients and finding the best answers to the challenges they face. Are you a pharmaceutical student at the end of your curriculum and have a strong interest in working with pharmaceutical and scientific documents, reports and publications? If yes then you may just be the pharmaceutical talent Fresenius Kabi is looking for. For more information about the placement and where to apply to check out the link below: http://bit.ly/IMPFreseniusKabi19 Deadline for applying is the 15th of September at 23:59 CEST.

Publié le 2019-09-08 - Par Caroline GUERIN

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Assistant chef de produits

Labatec - Genève (Suisse)

Labatec Pharma : Société privée et implantée en Suisse, Labatec est une compagnie pharmaceutique qui possède plus de 50 ans d’expérience dans la production et mise sur le marché de produits pharmaceutiques de haute qualité. Labatec développe et commercialise des médicaments qui contribuent à améliorer la qualité de vie de patients du monde entier, en parfaite synergie avec les besoins des secteurs hospitalier et retail. Fabriqués en Europe et approuvés par Swissmedic, nos produits représentent une marque pharmaceutique européenne de confiance. Notre vaste portefeuille comprend des produits injectables et oraux à usage hospitalier ainsi que des produits de spécialités, ciblant de multiples domaines thérapeutiques dont les pathologies musculosquelettiques et la santé de la femme. Missions principales : Au sein du département retail, nous recherchons un assistant chef de produit afin de soutenir les responsables de la gamme Gynécologie et Musculosquelettique pour le lancement de 2 produits de prescription innovants. Vous participerez à la mise en œuvre et au développement des campagnes marketing : - Proposer, ajuster et produire des outils promotionnels, en collaboration avec les services internes et les agences de communication en externe - Participer au développement digital des 2 gammes (Campagnes d’emailing, ajustement des supports de présentations pour les délégués médicaux, …) - Suivre et analyser la performance des produits ainsi que les données de performance des campagnes marketing - Participer à la mise en place de congrès et de séminaires Ce stage permet d’intégrer un environnement multiculturel et une entreprise internationale en forte croissance. Profil recherché : - Formation scientifique (Médecine, Pharmacie, Ecoles d’ingénieurs, Master scientifique etc…) +/- en commerce, marketing et/ou communication (Master, MS…) - Candidat faisant preuve de force de proposition et d’adaptabilité - Rigoureux et organisé, désirant travailler en équipe - Langues : Français et Anglais. L’Allemand serait un vrai plus Stage d’une durée de 5 mois minimum. Poste à pourvoir en septembre/octobre Localisé à Genève, Suisse Rémunération brute : 2500 CHF Merci d’envoyer votre CV et lettre de motivation à marketingch@labatec.com

Publié le 2019-07-31 - Par Caroline GUERIN

Du 2019-09-02
Au 2020-02-01

Stage
Pharmacovigilance Associate

PrimeVigilance - Prague (République-Tchèque)

PrimeVigilance is a dedicated pharmacovigilance, regulatory and medical information service provider with offices in Europe, UK and US. PrimeVigilance supports pharma, biotech and generics companies in managing the global safety of their products from early clinical trial development through to full post-marketing activities. PrimeVigilance has grown organically since 2008 and we now have over 500 people working from our six main offices in the United Kingdom, United States, Croatia, Czech Republic, Germany and Serbia. Web: www.primevigilance.com PLACEMENT Area: We are looking for a number of qualified and talented individuals to join us as Pharmacovigilance Associate. This opportunity would also be suitable for fresh Graduates as full training on pharmacovigilance activities and processes would be provided to them. Name: Pharmacovigilance Associate Description: The PV Specialist will be working as part of a project team, performing and supporting contracted pharmacovigilance activities on behalf of PrimeVigilance clients. Main Responsibilities: Intensive training at the beginning– face to face trainings, self-studies, colleagues shadowing Perform initial triage of the received safety notifications Process Individual Case Safety Reports (ICSRs), including data entry into the IRT ArisG safety database Follow-up ICSRs with the reporter, generate follow up (FU) queries and send FU requests Handle technical product complaints Perform ICSR reconciliations with business partners Review local literature screening search results, identifying ICSRs and other safety-related findings Participation during audits Location: Belgrade (Serbia) Duration: One year contract – possibility of permanent contract Salary: Competitive salary, exact remuneration depending on location Mandatory Qualifications: Degree in Pharmacy (or Medicine or Biology) Practical experience in pharmacovigilance is an advantage, but not a must Advanced knowledge of English Advanced knowledge of MS Word and Excel Excellent attention to detail and organizational skills Independent problem solving and decision-making skills Process oriented and critical thinking Responsible approach to work duties Preferable Qualifications: Practical experience in Pharmacovigilance in one or more of the areas of key responsibility. APPLICATION Requested Documents: CV and Motivational Letter (both in English) Deadline: 31st August 2019 More Info: central.imp@epsa-online.org | Central IMP Coordinator | Era Gruda vp.er@epsa-online.org | Vice-President of External Relations | Paulina Kruk

Publié le 2019-07-25 - Par Caroline GUERIN

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Pharmacovigilance Associate

PrimeVigilance - Zagreb (Croatie)

PrimeVigilance is a dedicated pharmacovigilance, regulatory and medical information service provider with offices in Europe, UK and US. PrimeVigilance supports pharma, biotech and generics companies in managing the global safety of their products from early clinical trial development through to full post-marketing activities. PrimeVigilance has grown organically since 2008 and we now have over 500 people working from our six main offices in the United Kingdom, United States, Croatia, Czech Republic, Germany and Serbia. Web: www.primevigilance.com PLACEMENT Area: We are looking for a number of qualified and talented individuals to join us as Pharmacovigilance Associate. This opportunity would also be suitable for fresh Graduates as full training on pharmacovigilance activities and processes would be provided to them. Name: Pharmacovigilance Associate Description: The PV Specialist will be working as part of a project team, performing and supporting contracted pharmacovigilance activities on behalf of PrimeVigilance clients. Main Responsibilities: Intensive training at the beginning– face to face trainings, self-studies, colleagues shadowing Perform initial triage of the received safety notifications Process Individual Case Safety Reports (ICSRs), including data entry into the IRT ArisG safety database Follow-up ICSRs with the reporter, generate follow up (FU) queries and send FU requests Handle technical product complaints Perform ICSR reconciliations with business partners Review local literature screening search results, identifying ICSRs and other safety-related findings Participation during audits Location: Belgrade (Serbia) Duration: One year contract – possibility of permanent contract Salary: Competitive salary, exact remuneration depending on location Mandatory Qualifications: Degree in Pharmacy (or Medicine or Biology) Practical experience in pharmacovigilance is an advantage, but not a must Advanced knowledge of English Advanced knowledge of MS Word and Excel Excellent attention to detail and organizational skills Independent problem solving and decision-making skills Process oriented and critical thinking Responsible approach to work duties Preferable Qualifications: Practical experience in Pharmacovigilance in one or more of the areas of key responsibility. APPLICATION Requested Documents: CV and Motivational Letter (both in English) Deadline: 31st August 2019 More Info: central.imp@epsa-online.org | Central IMP Coordinator | Era Gruda vp.er@epsa-online.org | Vice-President of External Relations | Paulina Kruk

Publié le 2019-07-25 - Par Caroline GUERIN

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Pharmacovigilance Associate

PrimeVigilance - Belgrade (Serbie)

PrimeVigilance is a dedicated pharmacovigilance, regulatory and medical information service provider with offices in Europe, UK and US. PrimeVigilance supports pharma, biotech and generics companies in managing the global safety of their products from early clinical trial development through to full post-marketing activities. PrimeVigilance has grown organically since 2008 and we now have over 500 people working from our six main offices in the United Kingdom, United States, Croatia, Czech Republic, Germany and Serbia. Web: www.primevigilance.com PLACEMENT Area: We are looking for a number of qualified and talented individuals to join us as Pharmacovigilance Associate. This opportunity would also be suitable for fresh Graduates as full training on pharmacovigilance activities and processes would be provided to them. Name: Pharmacovigilance Associate Description: The PV Specialist will be working as part of a project team, performing and supporting contracted pharmacovigilance activities on behalf of PrimeVigilance clients. Main Responsibilities: Intensive training at the beginning– face to face trainings, self-studies, colleagues shadowing Perform initial triage of the received safety notifications Process Individual Case Safety Reports (ICSRs), including data entry into the IRT ArisG safety database Follow-up ICSRs with the reporter, generate follow up (FU) queries and send FU requests Handle technical product complaints Perform ICSR reconciliations with business partners Review local literature screening search results, identifying ICSRs and other safety-related findings Participation during audits Location: Belgrade (Serbia) Duration: One year contract – possibility of permanent contract Salary: Competitive salary, exact remuneration depending on location Mandatory Qualifications: Degree in Pharmacy (or Medicine or Biology) Practical experience in pharmacovigilance is an advantage, but not a must Advanced knowledge of English Advanced knowledge of MS Word and Excel Excellent attention to detail and organizational skills Independent problem solving and decision-making skills Process oriented and critical thinking Responsible approach to work duties Preferable Qualifications: Practical experience in Pharmacovigilance in one or more of the areas of key responsibility. APPLICATION Requested Documents: CV and Motivational Letter (both in English) Deadline: 31st August 2019 More Info: central.imp@epsa-online.org | Central IMP Coordinator | Era Gruda vp.er@epsa-online.org | Vice-President of External Relations | Paulina Kruk

Publié le 2019-07-25 - Par Caroline GUERIN

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