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Job Details

Senior Regulatory Affairs Manager

Company: Clinical Professionals Ltd
Location: Germany
Reference: J25961
Closing Date: 05 Jan 17
Type: Full Time
Salary (£): On Application
Benefits:

Job Summary:

Senior Regulatory Affairs Manager Job type: Full-time, permanent: Germany A unique career opportunity has arisen at Regulatory Professionals. My client is one of the worlds most established and well-respected Medical Device Manufacturers

Requirements:

Senior Regulatory Affairs Manager
Salary: Competitive
Job type: Full-time, permanent
Location: Germany

A unique career opportunity has arisen at Regulatory Professionals. My client is one of the worlds most established and well-respected Medical Device Manufacturers, with sites across the EMEA and the US. They are looking for an experienced Regulatory Affairs Manager to join their operations in Germany.

Eligibility
The successful candidate will fulfil the following criteria:
*Having global Regulatory Affairs expertise for EU; Asia Pacific; Latin American Countries and US;
*Proven, high-level experience of the medical devices Regulatory sector in Europe, Product registration; CE Marking and dossier submission;
*Knowledge of other applicable international Regulatory requirements (FDA, 510(k));
*Solid understanding of medical devices Class II to III and in-depth expertise in the In Vitro Diagnostics, IVD, and therapeutic area is a must;
*German language to a native-level standard, with fluent English language skills is required;

Key responsibilities
Following their selection, the successful candidate will be responsible for the following areas:
*Regulatory dossiers creation, coordination and submission, across Europe and Latin America regions, to EU authorities and Notified bodies;
*Obtain Medical Device Licensing, Medical Device Establishment licensing, CE Marking and 510(k) clearance for Class I, Class II (a and b) and Class III medical devices in Europe;
*Obtain Regulatory approval for the marketing of devices across Classes I to III;
*Consulting on Regulatory Affairs matters pertaining to In Vitro Diagnostic devices;
*Provide expertise in MDD (Directive 93/42/EC), Quality requirements 21 CFR 820, ISO 13485 and Medical Device Risk Management ISO 14971.

Key words
Medical devices; medical technology; diagnostics; Regulatory; RA; Consultant; Consultancy; biotechnology; affairs; regulatory affairs; Specialist; officer; manager; VP; director; Germany; English; German; MDD; compliance; FDA; 510(k); 21; CFR; 820; 14971; 13485; Quality; Risk; Management; CE; Marking; CE mark; dossier; Notified body; IVD; In Vitro Diagnostic; IVD; EMEA; Americas; APAC; Switzerland; Austria;


In the event that you do not feel that this is the right role for you, please do not hesitate to forward these details on as we have a generous referral scheme in place.

Apply for this job: Senior Regulatory Affairs Manager

Contact Information:

Address:  Clinical Professionals UK
3rd Floor
33 Blagrave Street
Reading
Berkshire
RG1 1PW
England
Tel:  0044 118 959 4990
Fax:  0044 118 956 0607
Website:  Visit Our Web Site

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