Regulatory Affairs Specialist (m/w) in the northern part of Swi

Lawrence Harvey


Job ID :

11231


Company Type :

Staffing Firms


Industry :

Pharmaceuticals


Education Level :

Other


Address 1 :

Western Europe,Switzerland,Wil,


Key Skills :

Regulatory Affairs, EU/MDD, ISO 13485, asap, Switzerland, north


Salary :

Negotiable


Date Posted :

24 Apr, 2018



Company Name :

Lawrence Harvey


Location1 :

Wil




Job Category :

Regulatory Affairs Jobs


Experience :

Fresher


Job Type:

Permanent


Travel Amount:

100.00%





Description

Regulatory Affairs Specialist (m/w) in the northern part of Switzerland



Our customer collaborates with healthcare professionals around the globe to advance the pace of innovation in of medical devices. The products and solutions help treat patients suffering from disorders of, or injuries to, bones e.g.. Together with healthcare professionals, we help millions of people live better lives.

If you seize this opportunity, you will able to develop your international experience and be a part of a great and truly global team. Our client offers a wide range of challenging career advancement opportunities and a dynamic work environment.

For the European Headquarters we are looking asap for following profile:

Responsibilities:

* Prepares submission dossiers to support EMEA registration(s), re-registrations due to internal company or external government changes and renewals for expiring registrations
* Coordinates and reviews proposed product changes for impact on regulatory submission status of the product in EMEA
* Interpret and applies EMEA regulations to business practices and provide regulatory input, advice, and guidance to the organization
* Provide guidance to new entry-level associates

Your Qualifications and Experience:

* Degree in life sciences, technical (engineering) or related field (or non-US equivalent)
* At least 2 years of experience in regulatory field and working knowledge of and experience applying International medical device regulations and guidance documents.
* Knowledge of EMEA regulations (including labeling regulations) and knowledge of overall business environment, the orthopaedic industry and the marketplace.
* Excellent command of English and basic in German both verbal and written, ability to speak and write additional language would be an asset.
* Good computer skills, including Microsoft Office Suite.
* Ability to function well as a member of the team and build relationships between RA and other areas.
* Strong attention to detail, ability to multi-task and demonstrate strong writing and communication skills.

Möchten Sie mehr erfahren über unseren Kunden, den großen Gestaltungsfreiraum dieser Position und Ihre Entwicklungsmöglichkeiten? Dann übersenden Sie bitte Ihren CV sowie Ihre Zeugnisse unter Angabe von zwei Referenzen an Petra Ognjenovic: p.ognjenovic@sciproglobal.de. Bitte kontaktieren Sie im Falle von Rückfragen Frau Petra Ognjenovic unter: +41 43 5089217.

SciPro Global ist auf die Vermittlung von Experten aus den Bereichen Regulatory Affairs und Quality Assurance im Rahmen der Medizintechnik mit Fokus auf die D-A-CH Region spezialisiert. Die langjährige Erfahrung unserer Consultants bietet Ihnen neben einem großen Netzwerk an Kunden auch eine ausgezeichnete Branchenkenntnis sowie Beratung für den nächsten Schritt in Ihrer Karriere. Wir stehen für Qualität und freuen uns auf eine Zusammenarbeit mit Ihnen, denn uns ist am Herzen gelegen, dass die am besten qualifizierten Mitarbeiter mit dem entsprechenden Arbeitgeber in Verbindung gebracht werden.

Sollte Ihr Profil den Anforderungen entsprechen, setzen wir uns schnellstmöglich mit Ihnen in Verbindung.


Company Name:

Lawrence Harvey


Headquarters:

150 Leadenhall Street,London


Sector:

Staffing Firms


Country:

United Kingdom


Zipcode:

EC3V4TE


Website:

www.lawrenceharvey.com


Employees:

100 - 499


Industry:

Pharmaceutical Recruitment


City:

London


Phone No. :

0203 327 3072


Lawrence Harvey Life Sciences has exceptional relationships with the top talent and leading organisations in the Pharmaceutical and Medical Devices industry across the UK, USA, DACH region and the rest of Europe. Our consultants are experts within their specific areas and have a deep understanding of the full Life Sciences developmental cycle. As a client with a challenging role or a candidate with a niche specialism, you will receive a consultative service from people who truly understand the expectations and requirements of your industry. In an ever developing industry, an in-depth technical understanding and knowledge adds significant value and is imperative to ensuring our consultants are always up to speed, positioning ourselves perfectly to offer advice, analysis and support to our clients and candidates. We partner with leading pharmaceutical, medical device, generics, biotechnology, clinical research, R&D, manufacturing, regulatory affairs, CRO’s, CMO’s and medical communications organisations and have acquired an enviable and unrivalled reputation for delivering on niche, hard to fill and challenging positions. Our Specialisms within Life Sciences: Pharmaceuticals Medical Devices Regulatory Affairs Quality Assurance Quality Control Engineering Medical Affairs / Medical Information Qualified Persons Drug safety & Pharmacovigilance Biostatistics Clinical SAS Medical Writing Account Management & Business Development

For more information,visit www.lawrenceharvey.com.

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