Vaxcyte
Executive Director, Regulatory Affairs(m/w/x)
Full-timeFreelanceOn-siteSenior
Zug, Visp
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Developing regulatory strategy and policies for cardiovascular biopharmaceutical product launches. 10+ years relevant regulatory experience in biopharma, advanced degree in Law/Life Sciences required. Fast-paced biopharma environment, strategic leadership role.
Requirements
- Bachelor’s degree
- Advanced degree in Law, Life Sciences, Business, or related field
- 10+ years of relevant European Compliance experience
- Strong knowledge of European compliance frameworks and codes
- Experience in fast-paced, evolving environment
- Track record of building compliance programs
- Demonstrated ability to work at strategic and operational levels
- Excellent judgment, communication, and stakeholder management skills
- Ability to operate independently and influence without authority
- Ethics & Compliance certification (CCEP, CPA, CIA, etc.)
- Fluency in English
- Additional European languages (German, French, Spanish) highly desirable
- Strong interpersonal skills, including diplomacy and flexibility
Tasks
- Develop and refine the European compliance strategy
- Establish policies and procedures for country-specific regulations
- Serve as a Compliance business partner to regional leadership teams
- Act as a trusted advisor to stakeholders for product launch strategies
- Lead operational compliance activities, including material review and approval
- Deliver compliance training across functions and countries
- Monitor compliance activities and conduct risk assessments
- Manage local compliance operations while ensuring consistency
- Oversee third-party due diligence and vendor compliance processes
- Promote a culture of ethics and accountability throughout Europe
- Drive continuous improvement in compliance systems and reporting
- Support global compliance governance forums and strategies
- Assist in investigations of potential compliance violations
Work Experience
- 10 years
Education
- Bachelor's degreeOR
- Master's degree
Languages
- English – Business Fluent
- German – Basic
- French – Basic
- Spanish – Basic
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Cytokinetics 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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Developing regulatory strategy and policies for cardiovascular biopharmaceutical product launches. 10+ years relevant regulatory experience in biopharma, advanced degree in Law/Life Sciences required. Fast-paced biopharma environment, strategic leadership role.
Requirements
- Bachelor’s degree
- Advanced degree in Law, Life Sciences, Business, or related field
- 10+ years of relevant European Compliance experience
- Strong knowledge of European compliance frameworks and codes
- Experience in fast-paced, evolving environment
- Track record of building compliance programs
- Demonstrated ability to work at strategic and operational levels
- Excellent judgment, communication, and stakeholder management skills
- Ability to operate independently and influence without authority
- Ethics & Compliance certification (CCEP, CPA, CIA, etc.)
- Fluency in English
- Additional European languages (German, French, Spanish) highly desirable
- Strong interpersonal skills, including diplomacy and flexibility
Tasks
- Develop and refine the European compliance strategy
- Establish policies and procedures for country-specific regulations
- Serve as a Compliance business partner to regional leadership teams
- Act as a trusted advisor to stakeholders for product launch strategies
- Lead operational compliance activities, including material review and approval
- Deliver compliance training across functions and countries
- Monitor compliance activities and conduct risk assessments
- Manage local compliance operations while ensuring consistency
- Oversee third-party due diligence and vendor compliance processes
- Promote a culture of ethics and accountability throughout Europe
- Drive continuous improvement in compliance systems and reporting
- Support global compliance governance forums and strategies
- Assist in investigations of potential compliance violations
Work Experience
- 10 years
Education
- Bachelor's degreeOR
- Master's degree
Languages
- English – Business Fluent
- German – Basic
- French – Basic
- Spanish – Basic
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Cytokinetics 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
Cytokinetics
Industry
Pharmaceuticals
Description
Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on developing first-in-class muscle activators and inhibitors.
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