20 meilleures offres (regulatory affairs, bubendorf bl) (à pourvoir)

Intern: Environmental Compliance (Basel, 12 months, start: January 2027)
Roche —Bâle, BS
- 100%
- Anglais
- Niveau Master
- Bases de données
16 h
Integrated Medical Engagement Change Management Lead
Roche —Bâle, BS
- 100%
- Niveau Doctorat
- Gestion de projet
- Sans diplôme d'enseignement supérieur
Associate Director Market Access and Public Affairs DACH
Idorsia Pharmaceuticals Ltd. —Allschwil, BL
- 100%
- Télétravail
- Anglais
- Gestion de projet
- Leadership
EU Senior Global Reg Affairs Project Leader (m/f/d)
Viatris —Allschwil, BL
- 100%
- Télétravail
- Gestion du personnel
- Anglais
- Niveau Master
il y a 11 jours
Associate Director, Regulatory Operations, EMEA
Ultragenyx Pharmaceutical —Bâle, BS
- 100%
- Gestion du personnel
- Niveau Licence
- SharePoint
il y a 2 jours
Senior Manager, CRM Medical Affairs, EU/NM
BeiGene —Bâle, BS
- De 148 600 CHF à 185 700 CHF par an
- 100%
- Niveau Licence
- Leadership
- Compétences en communication
Executive Director, Regulatory Strategy
Neurocrine Bioscience —Allschwil, BL
- 100%
- Gestion du personnel
- Niveau Doctorat
- Niveau Master
Director, Clinical Quality Assurance
Neurocrine Bioscience —Allschwil, BL
- 100%
- Microsoft Outlook
- Niveau Master
- Esprit d'analyse
il y a 11 jours
Engagement Manager
NNIT A/S —Bâle, BS
- Gestion du personnel
- Anglais
- Niveau Master
il y a 9 jours
Clinical Development Lead
Idorsia Pharmaceuticals Ltd. —Allschwil, BL
- 100%
- Niveau Doctorat
- Niveau Master
- Compétences en communication
Associate Director, New Markets Integrated Insights
BeiGene —Bâle, BS
- De 159 600 CHF à 199 500 CHF par an
- 100%
- Microsoft Office
- Niveau Master
- Esprit d'analyse
Toxicology Expert
dsm-firmenich —Kaiseraugst, AG
- Niveau Doctorat
- Compétences rédactionnelles
- Anglais
Senior Biostatistician - Switzerland - Hybrid
Santhera —Pratteln, BL
- Niveau Doctorat
- Analyse de données
- Anglais
Client Partner, Strategy Consulting Large Pharma Advisory, 1 year contract
IQVIA —Bâle, BS
- 100%
- Compétences en communication
- Négociation
il y a 14 jours
Associate Director, Good Clinical Practice (GCP) Audit and Vendor Management
BeiGene —Bâle, BS
- De 105 800 CHF à 186 100 CHF par an
- 100%
- Télétravail
- Microsoft Powerpoint
- Microsoft Excel
- Microsoft Outlook
Senior Manager, Market Access Specialty Care
Sobi —Bâle, BS
- 100%
- Télétravail
- Niveau Doctorat
- Anglais
- Niveau Master
Postuler rapidement
Global Quality GVP Manager
Sobi —Bâle, BS
- 100%
- Travail hybride
- Gestion du personnel
- Niveau Licence
Postuler rapidement
Biostatistics Director
Neurocrine Bioscience —Allschwil, BL
- 100%
- Niveau Doctorat
- Analyse de données
- Recherche
Associate Scientific Director API Development, MSAT
Neurocrine Bioscience —Allschwil, BL
- 100%
- Gestion du personnel
- Niveau Doctorat
- Niveau Master
Senior Director, Medicine Development Leader
Sobi —Bâle, BS
- 100%
- Télétravail
- Anglais
- Leadership
- Compétences en communication
Postuler rapidement

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Intern: Environmental Compliance (Basel, 12 months, start: January 2027)

Roche -
Bâle, BS

Soumettre votre candidature

Détails de l'emploi

100%
Il y a 16 heures

Qualifications

Anglais
Niveau Master
Bases de données
Esprit d'analyse

Description complète du poste

Bei Roche kannst du ganz du selbst sein und wirst für deine einzigartigen Qualitäten geschätzt. Unsere Kultur fördert persönlichen Ausdruck, offenen Dialog und echte Verbindungen. Hier wirst du für das, was du bist, wertgeschätzt, akzeptiert und respektiert. Dies schafft ein Umfeld, in dem du sowohl persönlich als auch beruflich wachsen kannst. Gemeinsam wollen wir Krankheiten vorbeugen, stoppen und heilen und sicherstellen, dass jeder Zugang zur Gesundheitsversorgung hat – heute und in Zukunft. Werde Teil von Roche, wo jede Stimme zählt.

Die Position

Help shape the future of sustainable healthcare.

Global chemical and environmental regulations play a vital role in every stage of a product’s lifecycle — from development and manufacturing to usage and disposal. At Roche Pharma Technical Operations, we are uniting our expertise and expanding our capabilities to ensure strong compliance with these important regulations.

The Opportunity

In this role, you will work directly alongside ourEnvironmental Regulatory Experts to navigate highly complex global chemical policies, contributing to the compliance and sustainability of our life-saving products.

This internship offers a unique opportunity to gain hands-on experience in global environmental regulatory affairs within a leading pharmaceutical setting. Supported by senior experts, you will drive specific initiatives, including:

Regulatory Analysis& Impact Mapping: Monitor and analyze key global and regional regulations (such asEU/China REACH, Biocides, and EPR) to assess and document their impact on Roche Pharma operations.
Dossier& Registration Support: Collaborate with internal stakeholders and technical experts (e.g., ecotoxicologists) to gather data required for chemical and biocide registration dossiers.
External Study& Compliance Monitoring: Assist in tracking and monitoring testing studies conducted by external service providers for global chemical regulations.
Compliance Framework Development: Support the definition and digital implementation of a standardized global compliance oversight tool to ensure operational adherence.
Cross-Functional& Divisional Engagement: Actively participate in projects involving Pharma Sites, Diagnostics, and Diabetes Care to foster regulatory alignment and knowledge sharing

Who you are

Education

You are currently enrolled in, or have graduated from, a Master’s degree program in Environmental Regulations, Bio-engineering, Medical technical engineering Law with a focus on Env Law or Regulatory compliance, Chemistry or Chemical engineering (with knowledge of product regulations). Masters can be recently graduated within the last 12 months of starting the internship. PhD students must be enrolled for the entire duration of the internship.

Knowledge/ Skills/ Competencies:

Analytical skills: Ability to analyse complex regulations and regulatory guidance documents and translate them into easily understandable concepts.
Strong Collaboration: Team player who is comfortable working in a matrixed, multinational environment and building networks across different global sites.
Communication& Presentation: Fluent in English (written and verbal) with an aptitude for presenting complex technical data clearly.
Proactive& Independent: Self-motivated to take ownership of tasks and drive them to completion with guidance from mentors and subject matter experts.
Digital Proficiency: Strong competency with Google and or Microsoft Workspace, AI tools, and data analysis software, with an aptitude for working with regulatory compliance databases.

Application process:

Please upload a current CV and a Motivation Letter.

Additional Information:

Due to regulations, non-EU/EFTA citizens must be actively enrolled for the entire duration of the internship and provide an official university certificate stating that the internship is a mandatory part of their studies.
This internship position is located in Basel.
The start date for the internship is from January 2027 with a duration of 12 months.
Part-time employment and writing a thesis during the internship is not possible.

Ready to take the next step? We'd love to hear from you. Apply now to explore this exciting opportunity!

Wer wir sind

Eine gesündere Zukunft treibt uns zur Innovation an. Mehr als 100.000 Mitarbeiter weltweit arbeiten gemeinsam daran, wissenschaftliche Fortschritte zu erzielen und sicherzustellen, dass jeder Zugang zur Gesundheitsversorgung hat – heute und für zukünftige Generationen. Durch unser Engagement werden über 26 Millionen Menschen mit unseren Medikamenten behandelt und mehr als 30 Milliarden Tests mit unseren Diagnostik-Produkten durchgeführt. Wir ermutigen uns gegenseitig, neue Möglichkeiten zu erkunden, Kreativität zu fördern und hohe Ziele zu setzen, um lebensverändernde Gesundheitslösungen zu liefern.

Gemeinsam können wir eine gesündere Zukunft gestalten.

Roche ist ein Arbeitgeber, der die Chancengleichheit fördert.

Soumettre votre candidature

Affinez votre recherche

regulatory affairs emplois - bubendorf bl

Intern: Environmental Compliance (Basel, 12 months, start: January 2027)

Integrated Medical Engagement Change Management Lead

Associate Director Market Access and Public Affairs DACH

EU Senior Global Reg Affairs Project Leader (m/f/d)

Associate Director, Regulatory Operations, EMEA

Senior Manager, CRM Medical Affairs, EU/NM

Executive Director, Regulatory Strategy

Director, Clinical Quality Assurance

Engagement Manager

Clinical Development Lead

Associate Director, New Markets Integrated Insights

Toxicology Expert

Senior Biostatistician - Switzerland - Hybrid

Client Partner, Strategy Consulting Large Pharma Advisory, 1 year contract

Associate Director, Good Clinical Practice (GCP) Audit and Vendor Management

Senior Manager, Market Access Specialty Care

Global Quality GVP Manager

Biostatistics Director

Associate Scientific Director API Development, MSAT

Senior Director, Medicine Development Leader

Je souhaite recevoir la dernière alerte Emploi pour les postes de ce type : regulatory affairs (bubendorf bl)

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