Pharmiweb ChannelsAll | PharmaCo | Clinical Research | R&D/BioTech | Sales/Mktg | Healthcare | Recruitment | Pharmacy | Medical Comms

Pharmiweb.com RSS Feed Pharmiweb.com RSS Feeds

Job Details

RA / QA Specialist

Company: Clinical Professionals Ltd
Location: Warwickshire
Reference: JO-1810-418459
Closing Date: 29 Dec 18
Type: Full Time
Salary (£): 30,000 - 40,000
Benefits:

Job Summary:

This global Medical Technology organisation specialises in providing market leading Orthopaedic products to the Healthcare Industry.

Requirements:

Regulatory Affairs / Quality Assurance Specialist
Warwickshire
Industry: Medical Devices
Salary: 35K
Full time / Office based
Competitive salary and benefits


This global Medical Technology organisation specialises in providing market leading Orthopaedic products to the Healthcare Industry. Due to continuous growth they now have an exciting opportunity for a Regulatory Affairs & Quality Assurance specialist to join their highly professional team in Warwickshire.

Responsibilities
Representing the Regulatory Affairs & Quality Assurance function for all Field Safety Corrective Actions (FSCA), including reporting related activities to the competent authorities
Assisting the Group Manager with other RA duties as required
Dealing with product registrations
Managing certificates with the MHRA
Acting as a single point of contact with the UK & Ireland Competent Authorities for FSCA and related matters
Collating and reporting evidence of FSCA closure for each affected country within EU & Canada region
Developing and assisting in product registrations & re-registrations, including the supply of necessary documents (e.g. certificates of the marketability, authentications, etc) for Europe & Canada and to existing approved countries for their products. Working with the MHRA in managing and obtaining Free Sales Certificates, legal for Notary signatures and Embassies for Legalisation of documents for the customers.
Assisting in the development, reviewing and implementing regional policies and procedures based on corporate and regional requirements (e.g. current MDD and new MDR coming into force)

Successful candidates will have the followings skills & experience:
Experience of working within Regulatory Affairs within the Medical Devices sector Essential
Previous experience of working within the Quality Assurance department, working to ISO 13485 standards Essential
Global experience of dealing with the MHRA is also required for this role Essential
You will also have experience of dealing with recalls Essential

Please note in order for your application to be successful you must hold a valid right to work document for the UK as no sponsorship is offered.

To apply for this role please send your CV through to Kully Sahota, Senior Consultant, Kully.sahota@medtechprofessionals.com or call 0207 822 1710 for more information

Apply for this job: RA / QA Specialist

Contact Information:

Address:  Clinical Professionals Ltd
33 Blagrave Street,
Reading
RG1 1PW
England
Tel:  0118 959 4990
Fax:  0118 956 0607
Website:  Visit Our Web Site

Advertising
Site Map | Privacy & Security | Cookies | Terms and Conditions

PharmiWeb.com is Europe's leading industry-sponsored portal for the Pharmaceutical sector, providing the latest jobs, news, features and events listings.
The information provided on PharmiWeb.com is designed to support, not replace, the relationship that exists between a patient/site visitor and his/her physician.