Idorsia Pharmaceuticals Ltd
Senior Technical Regulatory Affairs Manager(m/w/x)
Full-timeOn-siteSenior
Basel
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BRBrenntag Schweizerhall AG
Swiss Regulatory Affairs Specialist(m/w/x)
Basel
Full-timeOn-siteSenior
Nejo AI Summary
Supporting EMEA divisions with raw material regulatory compliance and documentation. Swiss Medic and European NCA regulations knowledge required. Good pension plan, health insurance.
Requirements
- Degree or considerable life sciences experience
- Knowledge of pharmaceutical industry regulations (APIs, excipients, biopharma, traditional pharma raw materials)
- Knowledge of Swiss Medic and European NCA regulations for API, excipient, raw material distribution
- Good collaboration and communication skills
- Proactive work across all levels and functions
- Understanding of current raw material regulations (traditional Pharma, Biopharma)
- Ability to resolve compliance issues
- Ability to respond to complex regulatory queries
- Flexibility in adapting to changing regulations
- Flexibility in adapting to changing industry standards
- Flexibility in adapting to changing project demands
Tasks
- Support EMEA divisions on raw material supply topics
- Address regulatory, legal, compliance, quality, and safety issues
- Complete technical and regulatory documentation for customers
- Respond to customer information requests in English
- Source information from internal teams and suppliers
- Report and document customer requests using KPIs
- Collaborate with commercial and value-added services teams
- Lead regulatory topics for customer projects
- Collaborate with QHSE and supply chain teams
- Ensure regulatory compliance with current standards
- Support implementation of new standards (IPEC GMP/GDP, EXCiPACT, GDP)
- Collaborate within the Pharma Regulatory team on global projects
- Create and manage product regulatory information
- Provide training on regulatory topics to commercial teams
- Provide training on regulatory topics to supply chain teams
- Support the commercial success of the Pharma business unit
Work Experience
- approx. 4 - 6 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
- German – Business Fluent
- Swiss German – Business Fluent
Benefits
Retirement Plans
- Good pension plan
Healthcare & Fitness
- Health insurance
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Brenntag Schweizerhall AG 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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BRBrenntag Schweizerhall AG
Swiss Regulatory Affairs Specialist(m/w/x)
Basel
Full-timeOn-siteSenior
Nejo AI Summary
Supporting EMEA divisions with raw material regulatory compliance and documentation. Swiss Medic and European NCA regulations knowledge required. Good pension plan, health insurance.
Requirements
- Degree or considerable life sciences experience
- Knowledge of pharmaceutical industry regulations (APIs, excipients, biopharma, traditional pharma raw materials)
- Knowledge of Swiss Medic and European NCA regulations for API, excipient, raw material distribution
- Good collaboration and communication skills
- Proactive work across all levels and functions
- Understanding of current raw material regulations (traditional Pharma, Biopharma)
- Ability to resolve compliance issues
- Ability to respond to complex regulatory queries
- Flexibility in adapting to changing regulations
- Flexibility in adapting to changing industry standards
- Flexibility in adapting to changing project demands
Tasks
- Support EMEA divisions on raw material supply topics
- Address regulatory, legal, compliance, quality, and safety issues
- Complete technical and regulatory documentation for customers
- Respond to customer information requests in English
- Source information from internal teams and suppliers
- Report and document customer requests using KPIs
- Collaborate with commercial and value-added services teams
- Lead regulatory topics for customer projects
- Collaborate with QHSE and supply chain teams
- Ensure regulatory compliance with current standards
- Support implementation of new standards (IPEC GMP/GDP, EXCiPACT, GDP)
- Collaborate within the Pharma Regulatory team on global projects
- Create and manage product regulatory information
- Provide training on regulatory topics to commercial teams
- Provide training on regulatory topics to supply chain teams
- Support the commercial success of the Pharma business unit
Work Experience
- approx. 4 - 6 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
- German – Business Fluent
- Swiss German – Business Fluent
Benefits
Retirement Plans
- Good pension plan
Healthcare & Fitness
- Health insurance
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Brenntag Schweizerhall AG 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.
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
About the Company
Brenntag Schweizerhall AG
Industry
Pharmaceuticals
Description
Das Unternehmen bietet gleiche Beschäftigungsmöglichkeiten und schätzt Unterschiede zur Förderung von Innovation.
Not a perfect match?
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