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Head of Regulatory Affairs Austria and Switzerland (m/f/d) – fixed term for 18 months
看过: 163
更新日: 26-03-2024
类别: 法律/合同
水平: Director
工作类型: Full-time
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工作内容
7087 Mylan Pharma GmbHAt VIATRIS, we see healthcare not as it is but as it should be. We act courageously and are uniquely positioned to be a source of stability in a world of evolving healthcare needs.
Viatris empowers people worldwide to live healthier at every stage of life.
We Do So Via
Access – Providing high quality trusted medicines regardless of geography or circumstance;
Leadership – Advancing sustainable operations and innovative solutions to improve patient health; and
Partnership – Leveraging our collective expertise to connect people to products and services.
Key Responsibilities For This Role Include
Every day, we rise to the challenge to make a difference and here’s how the Head of Regulatory Affairs role -fixed term for 18 months for our Swiss and Austrian sites will make an impact:
- Research and keep informed of updates EU and CH Regulatory legislations and guidance as they pertain to pharmaceuticals, Medical devices, food supplements and cosmetics
- Provide interpretation of EU and CH policies and procedures
- Establish and provide strategic leadership and oversight of the Regulatory function
- Attend and participate in authority inspections and meetings as well as lead regulatory discussions with local Health authority
- Support the coordination of Drug and Medical Device Recalls and Advisory Notices
- Oversee all regulatory documentation prepared and submitted, monitor compliance and report progress periodically as require by corporate management
- Support the maintenance of operational/expense budget and capital budget for the Regulatory Affairs Department
- Provide regulatory support and leadership on internal cross-functional project teams
- Review and maintain local compliance program Review promotional material/ marketing material (incl. online media) for Scientific and regulatory compliance
- Medical, Pharmacy or Life-sciences University degree (or equivalent), PhD preferred
- Minimum 5 years of working experience within the pharmaceutical industry and within Regulatory Affairs
- Very good knowledge of national, EU and Swiss regulations and regulatory guidance, policies and procedures
- Profound knowledge of Medical Device regulations
- Demonstrate ability to provide quality work using strong organizational, facilitation and interpersonal skills in a cross-functional team locally
- Possess an excellent interpersonal, verbal, and written communication skills in English and German
- Experienced in leading and working in cross-functional teams
- Experienced in leading and working in a virtual team
Viatris is an Equal Opportunity Employer.
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最后期限: 10-05-2024
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