IQVIA Biotech
Clinical Associate Submissions – Regulatory(m/w/x)
Full-timeWith HomeofficeJunior
Berlin
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TH
The Force CT GmbHRegulatory Affairs Manager(m/w/x)
Berlin
Full-time, Part-timeWith Home Office
Description
As a Regulatory Affairs Manager, you will navigate the complexities of regulatory submissions and strategies, ensuring compliance while supporting international customers, particularly in the German market. This role involves a mix of technical writing, project management, and regulatory expertise across various product types.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •Academic degree in pharmacy or related scientific field
- •Strong communication skills
- •Oral and written proficiency in English and German
- •Strong project management skills
- •Excellent teamwork skills
- •Attention to detail
- •Business fluency in German
Education
Bachelor's degree
Tasks
- •Develop regulatory strategies for marketing authorization applications
- •Manage life-cycle measures and local regulatory activities
- •Conduct technical and medical writing
- •Handle regulatory submissions, including eCTD publishing
- •Oversee submission and procedure management
- •Ensure compliance with labeling requirements
- •Support global and European regulatory projects
- •Provide expertise on EU and international regulatory procedures
- •Assist international customers in the German market
Languages
German – Business Fluent
English – Business Fluent
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of The Force CT GmbH and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
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(Senior) Sales and Alliance Manager(m/w/x)
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QP / Qualified Person / Sachkundige Person(m/w/x)
Full-time/Part-timeWith HomeofficeExperiencedHeidenheim an der Brenz, Berlin, Hamburg
TH
The Force CT GmbHRegulatory Affairs Manager(m/w/x)
Berlin
Full-time, Part-timeWith Home Office
New Job?Nejo!
The AI Job Search Engine
Description
As a Regulatory Affairs Manager, you will navigate the complexities of regulatory submissions and strategies, ensuring compliance while supporting international customers, particularly in the German market. This role involves a mix of technical writing, project management, and regulatory expertise across various product types.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •Academic degree in pharmacy or related scientific field
- •Strong communication skills
- •Oral and written proficiency in English and German
- •Strong project management skills
- •Excellent teamwork skills
- •Attention to detail
- •Business fluency in German
Education
Bachelor's degree
Tasks
- •Develop regulatory strategies for marketing authorization applications
- •Manage life-cycle measures and local regulatory activities
- •Conduct technical and medical writing
- •Handle regulatory submissions, including eCTD publishing
- •Oversee submission and procedure management
- •Ensure compliance with labeling requirements
- •Support global and European regulatory projects
- •Provide expertise on EU and international regulatory procedures
- •Assist international customers in the German market
Languages
German – Business Fluent
English – Business Fluent
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of The Force CT GmbH and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
About the Company
The Force CT GmbH
Industry
Healthcare
Description
Das Unternehmen baut Firmen im Gesundheits- und Pharmasektor auf und fördert ein flexibles Arbeitsumfeld.
Not a perfect match?
- IQVIA Biotech
Clinical Associate Submissions – Regulatory(m/w/x)
Full-timeWith HomeofficeJuniorBerlin - Vara
Quality Manager in Regulatory Affairs(m/w/x)
Full-timeWith HomeofficeExperiencedBerlin - Flinn.ai
Customer Relationship & Success Manager(m/w/x)
Full-timeWith HomeofficeExperiencedBerlin, Wien - CHEPLAPHARM Arzneimittel GmbH
(Senior) Sales and Alliance Manager(m/w/x)
Full-timeWith HomeofficeSeniorGreifswald, Berlin - The Force CT GmbH
QP / Qualified Person / Sachkundige Person(m/w/x)
Full-time/Part-timeWith HomeofficeExperiencedHeidenheim an der Brenz, Berlin, Hamburg