...industry and the academic sphere.
Job Description
One of Sobi’s four strategic pillars is to “Go Global”. The Manager, Regulatory Affairs International supports our ambitious geographical expansion plans. Sobi is seeking to register some of our existing portfolio...
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Vollzeit
Job Purpose
Be a member of product development project-teams from the initiation phase, ensure implementation of quality and Regulatory Affairs requirements for Europe, US & Canada, perform product registration in EU, US & Canada.
Main Tasks and Responsibilities...
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Vollzeit
...compliance with regulations throughout product development.
- Conduct regulatory research and prepare documentation for submissions.
- Support... ...- Bachelor's degree in a relevant field.
- Prior regulatory affairs experience
- general pharma knowledge
Ausbildung
Regulatory...
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Temporär
...disease. Our edge comes from our team of people and our commitment to patients.
The CMC Dossier Manager plays a crucial role in developing the technical eCTD sections to support Regulatory CMC dossier applications. They work with limited guidance from the manager and are...
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Postdoc Stelle
Senior Consultant Regulatory Affairs MedTech (SaMD, AI, Robotics)
Compliance Services - Basel, Frankfurt
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About Arcondis
Arcondis is a global consulting company with an exclusive focus on the healthcare and life science industries. Headquartered...
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...work.
For our fastgrowing team we are looking for a Programme Director reporting to the SVP Global Head of Pharma Operations. In this... ...drug development plans that are patient focused and address regulatory commercial and access considerations
Drive decisionmaking...
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Vollzeit
...Switzerland.
Job Description
Do you have a Master degree or a PhD in Science? Are you looking to grow a new career in the Regulatory field? If so, we have a fantastic and unique opportunity to join Syngenta Global Regulatory Team based in Basel. You will take an...
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The diverse and interesting range of responsibilities includes:
Developing, planning and implementing strategies that align with business goals in order to maximize business growth based on business targets to support and promote business growth of River Advice AG
...
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Ihre Aufgaben
~Mitarbeit bei der Erstellung, Einreichung und Dokumentation des regulatorischen Meldewesen EU (CoRep, FinRep, LiqRep und weitere Unterlagen gemäss Konzernvorgaben) inkl. notwendigem KnowHow Aufbau zur Betreuung der relevanten EDV-Systeme und Schnittstellen...
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Summary
We are seeking a Digital Innovation Director to join our team. The purpose of the Digital Innovation Director is a key organizational position which partners with colleagues across all Franchises, Functions, Novartis Divisions and external channels to drive...
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...Novartis Pharma AG
Medical Director - Dermatology Translational Medicine
Job ID
392731BR
Feb 27, 2024
Switzerland
About... ...of mechanistic studies and profiling packages that meet regulatory requirements and support differentiated and competitive drug labeling...
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Novartis Pharma AG
Basel BS
Vor 25 Tagen
...this very exciting career opportunity! The role of a Project Director - CQV:
Provide cGMP leadership and guidance for the integration... ...Industries; Sound technical knowledge of EU and global regulatory requirements. Proficient in cGMP standards.
~ Experience in...
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Vollzeit
Job Title: Event Manager Clinical Development & Medical Affairs
Work Location: Allschwil
Country: Switzerland
Schedule: Parttime (80%)
Desired start date: ASAP
Duration: 12 months
Contractor Rate: CHF 69.49 - CHF 77.96
RESPONSIBILITIES AND TASKS
• Plan, coordinate...
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Teilzeitarbeit
Soforteinstellung
Regional Director Basel 100% (a)Arbeitsort:BaselPensum:100%Arbeitsbeginn:per sofort oder nach VereinbarungBei ISS bezeichnen wir uns alle als Placemakers. Unser Ziel ist es, dass unsere Kunden an ihrem Arbeitsplatz eine optimale Umgebung vorfinden und sich wohlfühlen....
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...Novartis AG
Medical Director - Translational Medicine (Neuroscience)
Job ID 384547BR Mar 05, 2024 Switzerland
About the Role... ...foster communication with crucial collaborating investigators, regulatory authorities, and other stakeholders
• The work environment is...
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Vollzeit
Schichtarbeit
Novartis AG
Basel BS
Vor einem Monat
...Lonza AG
Director, MES Program Lead (m/f/d)
Switzerland, Basel
Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented...
Lonza AG
Basel BS
Vor einem Monat
...Du bist fit in Print und Web, teamfähig, motiviert und hast einige Jahre Berufserfahrung?
Dann bist du die oder der Junior Art Director, den wir suchen!
Junior Art Director 70–100%
Deine Mission: Als Junior Art Director bei yuni wirst du Teil eines dynamischen Teams...
yuni Kommunikation GmbH
Basel BS
Vor 20 Tagen
About the Role
The Clinical Development Medical Director (CDMD) is responsible for leading the strategic planning and management of... ...development of clinical sections of trial and program level regulatory documents
• Driving execution the assigned clinical program...
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Flexible Arbeitszeit
...Proof of Concept by delivering key Profiling data to support regulatory submissions
• As a recognized expert in your field, you drive... ...organizations
Role Requirements
This position is written for Director - we can hire Associate Director for those with careers that...
Vollzeit
Postdoc Stelle
...About the role
The Clinical Development Director (CDD) in the Cardiovascular, Renal & Metabolic (CRM) Development Unit is responsible... ...review, program specific standards, clinical components of regulatory documents/registration dossiers, and publications
• Leading...
Vollzeit
CDD
Flexible Arbeitszeit
...About the role
The Associate Director, Global Program Management, Oncology, will provide project management expertise as an individual contributor to early-stage drug development programs. The key to success will include working across a global team, building impactful...
Vollzeit
About the Role
Over 800 biomarker discovery and development projects, across more than 100 clinical studies, which generate 20 petabytes of patient data! All waiting for you to unlock the next breakthrough in medicine.
Biomarkers are critical components of translational...
Postdoc Stelle
...that create a frictionless user experience.
As an Associate Director Product Growth Manager you flexibly engage to lead diverse... ...management.
• You ensure adherence to security, quality, and regulatory standards and policies, including GxP compliance if applicable...
Vollzeit
...Basel, Switzerland (hybrid)
The Clinical Development Medical Director (CDMD) is responsible for leading the strategic planning and... ...Leading development of clinical sections of trial and program level regulatory documents
• Driving execution the assigned clinical program...
Vollzeit
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Flexible Arbeitszeit
...disrupt the market and challenge established players with its cutting-edge products. We are seeking a dynamic and experienced Sales Director to lead the EMEA market launch and expansion and play a pivotal role in commercializing the Alliedstar portfolio through channel...
Vollzeit
...Resilient, energetic, and enthusiastic; responding constructively to challenging new ideas and input
This position is written for Director level; however, we can hire Associate Director that may have less established scientific and/or clinical trial experience but has...
Vollzeit
Postdoc Stelle
...promising career opportunities and offer the latest in skill development training programmes.
Contract Manager within Global Medical Affairs – 5854 LBD
We are looking for a highly motivated Contract Manager within Global Medical Affairs for our client, a major...
Homeoffice
...correlations to optimize method performance.
6) Regulatory Compliance : Ensure compliance with... ..., quality assurance, and regulatory affairs, to align method development activities with... ...experience in biotechnological CMC development
Ability to work in a matrix...
...You will help leading analytical activities within a Technical CMC project team (e.g., hep to define control and specification setting... ...valuable input to the analytical CMC documents and support regulatory submissions.
• Manage interactions and contribute to a high level...
...supplier/CMO evaluations.
Lead issue resolution and QA review for CMC teams and Supply chain stakeholders.
Initiate quality... ...qualification status.
Write edit assess and approve relevant regulatory documents and support audits.
Actively support the organization...
Vollzeit