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Job Details

German Speaking Regulatory Affairs Specialist

Company: CK Clinical
Location: Berkshire
Reference: CL40561
Closing Date: 07 Dec 17
Type: Contract
Salary (£): Competitive
Benefits:

Job Summary:

Mary Bolt is recruiting for a German speaking Regulatory Affairs Specialist to join a world leading medical device organisation that develop and manufacture speciality products...

Requirements:

Mary Bolt is recruiting for a German speaking Regulatory Affairs Specialist to join a world leading medical device organisation that develop and manufacture speciality products for all surgical fields at their site based in Berkshire on a contract basis. This is a contract position with an initial duration of 4 months (although highly likely to extend) and the hourly rate on offer is up to £40phr.

The company:
Our client is one of the worlds leading medical device organisations with an extensive portfolio of surgical technology and specialty solutions. This pioneering company focuses on advancing patient care and are committed to helping to address the world's most pressing healthcare issues.

Location:
This role is located in their offices on a lovely secluded site in Berkshire and is a 30 minute drive away from Reading, a vibrant and cultural city with plenty of shopping, history and architecture. They are also a 30 minute drive from Heathrow airport. The site is easily commutable by car from the M4 corridor and the surrey area as well as having good public transport links with London.

The role:
You will be responsible for providing Regulatory Affairs support to one of the company's European Authorised Representatives (EAR) and filing and maintaining medical device registrations in the relevant German national database, maintaining internal documentation and communicating registration information to relevant stakeholders. You will also assist with all responsibilities held by the European Authorised Representative based in Germany and prepare status updates for senior management on the progress of medical device registrations completed in Germany for the EAR as well as being responsible for the submission of regulatory documentation and data into the German Regulatory system.

Your background:
Ideal candidates must have experience of working in Regulatory Affairs and handling European Medical device Registrations (ideally across Germany). Candidates must be fluent in both written and spoken German and English.

The benefits:
This role is offering a competitive rate and is a great opportunity to work in a global prestigious company with opportunities for continuous growth and outstanding training programmes.

Please note that your CV should show exact dates of employment (month and year) and any gaps of a month or more should be explained.

CK Group is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria.

If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential. Please quote reference CL40561 in all correspondence.

Apply for this job: German Speaking Regulatory Affairs Specialist

Contact Information:

Address:  Head Office
9 High Street
Stevenage
Hertfordshire
SG1 3BG
England
Tel:  +44 (0)1438 743047
Fax:  +44 (0) 1438723800
Website:  Visit Our Web Site

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