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Technical Regulatory Manager - Switzerland - Permanent
at SEC Pharma in Switzerland
Technical Regulatory Manager – Switzerland – Permanent
My client is a large global pharmaceutical company, which is currently looking for an experienced Technical Regulatory Manager to join their team of top professionals based in their office in Switzerland. You need to be experienced with all regulatory activities to do with the quality regulatory documentation (CMC, Module 3) required for Clinical trial and Marketing approval for FDA and EMA.
Responsibilities:
• Strategic leadership and regulatory decision making for multiple small molecule and peptide development products
• Represent the technical regulatory function of the company
• Shape the technical regulatory strategy within international project teams
• Coordinate the preparation and filing of the quality regulatory documentation
• Participate in international health authority meetings
Requirements:
• At least a Bachelor’s Degree, but preferably a PhD degree in pharmaceutical sciences, chemistry or related technical fields
• Minimum 5 years of experience in technical regulatory, pharmaceutical development, production or quality.
• Good knowledge of Global regulatory requirements
• Excellent written and oral communication, presentation and negotiation skills
• Fluent spoken and written English and a good knowledge of German are a must.
This is a fantastic chance to work for a company where you have the opportunity to pursue your interests across functions and geographies, and where a job title is not considered the final definition of who you are, but the starting point.
Please, send your CVs to Nikolay.Dimitrov@secpharma.com
Or
Call +44 (0)20 7255 6600 and talk to Nikolay Dimitrov
My client is a large global pharmaceutical company, which is currently looking for an experienced Technical Regulatory Manager to join their team of top professionals based in their office in Switzerland. You need to be experienced with all regulatory activities to do with the quality regulatory documentation (CMC, Module 3) required for Clinical trial and Marketing approval for FDA and EMA.
Responsibilities:
• Strategic leadership and regulatory decision making for multiple small molecule and peptide development products
• Represent the technical regulatory function of the company
• Shape the technical regulatory strategy within international project teams
• Coordinate the preparation and filing of the quality regulatory documentation
• Participate in international health authority meetings
Requirements:
• At least a Bachelor’s Degree, but preferably a PhD degree in pharmaceutical sciences, chemistry or related technical fields
• Minimum 5 years of experience in technical regulatory, pharmaceutical development, production or quality.
• Good knowledge of Global regulatory requirements
• Excellent written and oral communication, presentation and negotiation skills
• Fluent spoken and written English and a good knowledge of German are a must.
This is a fantastic chance to work for a company where you have the opportunity to pursue your interests across functions and geographies, and where a job title is not considered the final definition of who you are, but the starting point.
Please, send your CVs to Nikolay.Dimitrov@secpharma.com
Or
Call +44 (0)20 7255 6600 and talk to Nikolay Dimitrov
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