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Responsable affaires rglementaires

Location Lyon, United Kingdom
Posted 06-December-2018
Description

Vacancy Details

My client, a fast-growing Medical Device company based in Lyon Area are looking for an RA manager. A great opportunity to join an expanding team with a great portfolio of products.

Responsable affaires rglementaires

Location : Lyon Area

Rmunration selon profil

CDIpourvoir ds maintenant

Responsabilits

* Rattach directementla direction gnrale

* Prparation et suivi des dossiers rglementaires

* Gestion des enregistrements des donnes techniques selon la rglementation en vigueur
* Validation des procds spciaux

Candidate criteria

* Droit de travailler en France
* 2+ annes dexprience en affaires rglementaires dans le pharmaceutique (ou dispositif mdicaux)
* Exprience des rglementations Europen (Globale dsirable)
* Anglais courant crit et orale

Looking but this isnt the right position for you?

If you are interested in a new opportunity but your experience doesnt fit this role, please email your CVor call 00 44 203 589 9296 for a confidential discussion about potential opportunities.

NOT OF INTEREST TO YOU BUT KNOW SOMEONE IT WOULD BE?

JCW offer a generous referral scheme reward, whereby anyone who refers us to a successfully placed candidate is entitled to up to 250 worth of vouchers.

Catalyst Life Sciences

CLS is a global recruitment company operating in the Life Sciences space, with specialist consultants working within the technical and regulatory areas. This includes the following markets;

* Pharmacovigilance/Drug Safety
* Regulatory Affairs
* Quality Assurance
* Quality Control
* Medical Information
* Medical Writers
* Medical Affairs
* Compliance
* Audit
* Validation
* Production
* Manufacturing
* Clinical Trials
* Clinical Research
* Project Management
* Finance

My Linked In Profile

(url removed)/in/cheikh-khoule

I personally specialise in recruiting QA and validation professionals for roles across the UK so please do get in touch should you be considering new roles or looking to fill ones at your current company!

KEYWORDS

Medical / device / ISO / 13485 / FDA / 9001 / QMS / 62304 / quality / assurance / engineer / Regulation / MDD / MDR / 1471 / Design / Validation / risk / assessment / SRS / pharmaceutique

 
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