Regulatory Affairs Specialist/ Manager - Central Swiss- Pharma

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Schlagworte

Beschreibung

An international pharmaceutical company based in the surrounding areas of Zurich and Zug are currently seeking a Regulatory Affairs professional to join a specific division within their Swiss headquarters.

The position is a specialist role. Within the position a senior and experienced regulatory affairs professional will report directly into the Head of RA and will ensure that all regulatory aspects are covered with a view to ensure products are compliant for the Swiss market.

Within your job duties you will act as a go to person for all regulatory requirements as well as ensuring that local market needs are understood and aligned to the global regulatory strategy of the company. As the specialist, or indeed regulatory expert you will liaise with a number of departments throughout the business including commercial, marketing, quality and R&D.

The successful applicant will have a very strong knowledge within Regulatory Affairs including the preparation of product license applications and have exposure to Licensed products, medical devices, cosmetics and food. You will also be responsible for Swiss submissions so previous experience with Swiss Medic is required. In addition you should speak German and English, and French would be an advantage.

For further information, please contact Ed Bevans at Real Pharma on or email me directly to Additionally, if you have read this and feel this role isn't ideal for you, but you are looking for a new position within regulatory affairs, please do not hesitate to contact me for a consultation.

To find out more about Real please visit www.realstaffing.com
Start
01/2014
Von
Real Staffing
Eingestellt
11.10.2013
Projekt-ID:
611423
Vertragsart
Festanstellung
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