Regulatory Affairs Manager - MD
- Employer
- NonStop Consulting
- Location
- Zürich
- Salary
- Negotiable
- Closing date
- Dec 29, 2018
View more
- Sector
- Pharmaceutical, Regulatory Affairs
- Contract Type
- Employee
- Hours
- Full Time
- Organization Type
- Corporate
Job Details
Your Responsibilities
* Prepare international submissions
* Develop and write clear arguments and explanations for new product certifications and license
renewals
* Monitor and set timelines for certification and/or license variations and renewal approvals
* Collect, collate and evaluate scientific data that has been researched by colleagues
* Provide input to project teams during the development of regulatory plans & filing strategy to
ensure acceptable labelling in markets assigned
* Provide regulatory intelligence information to the organization
* Monitor the regulatory competitor landscape and keep the organization abreast of potential
threats and opportunities jeopardizing global development goals
* Stay abreast of current and new legislation related to medical devices
Company
Our Consultants are trained to deliver an exceptional standard of recruitment services to clients across the life sciences, chemical, care, educations, technical, digital and finance industries.
Our clients – and bottom line profits - tell us that we do a great many things very well. Complacency, however, is the last word you would associate with us. We work incredibly hard to deliver better and better results, based on stronger and stronger service delivery. Which is why we believe the best is yet to come – for us, our clients and for the people who have what it takes to join us on the journey.
The result? We’re expanding (in the UK and across Europe and even to Boston, US) and continue to post impressive performances in all our niche sectors.
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