Regulatory Affairs Manager

vor 2 Wochen

Zurich, Schweiz Pfizer Vollzeit

Regulatory Affairs Manager (M/F/d)

80-100%

This is what you can look forward to:

- Overseeing assigned product portfolio of innovative prescription drugs with complex regulatory background
- Handling entire regulatory lifecycle from initial MAAs to line extensions, labeling and CMC variations, renewals, PSUR submissions, etc.
- Developing of submission strategies to enhance the product value and expedite pathways
- Collaborating with local and global regulatory and cross-functional colleagues
- Acting as reliable and competent contact for Swissmedic

What you offer:

- Academic degree in natural sciences
- Preferably experience in Swiss Regulatory Affairs
- Knowledge of the current Swiss regulatory and drug laws environment and/or about other legal environments (EU, US, etc.) is of advantage
- Knowledge of or experience in project management techniques is of advantage
- Strong skills in productivity, organizational and time management
- Highest quality standards
- Demonstrated ability to foster teamwork
- Very good knowledge of German and English, good knowledge of French and/or Italian is of advantage
- Solid knowledge of pharmaceutical analytics technology, pharmacology, toxicology and medicine
- Good computer skills

What we offer:

- An attractive overall employment package (compensation, vacation, pension) in a world-leading company
- An exciting, fast-paced environment
- Friendly, open and collaborative company culture
- Being part of a local as well as an interdisciplinary team
- Flexible working hours
- Opportunities to engage in social projects
- Company-paid health activity program
- Great growth
- and development opportunities
- Health programs for all employees
- The opportunity to engage in social projects

Convinced?

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