• Contract
  • Dublin

Website Independent Search Solutions Ltd

My client a Medical Device Distributor has a position for a Regulatory Affairs Specialist to come on board for a 12 Month Project.

 

Your primary function will be associated with the new Medical Device Regulations within Europe (EUDR); and ensuring that the company is completely compliant.

 

This role will require occasional travel between the companies offices in Dublin, Belfast and in England (All travel expenses covered).

 

I am keen to speak with candidates who have exposure to European Medical Device Regulations and have worked in Regulatory Affairs.

 

A Mid-Level position the package will reflect a competitive rate plus other benefits – APPLY TODAY

 

Regulatory Affairs Specialist / Regulatory Affairs Advisor / Regulatory Affairs Officer / RA Specialist / Medical Device Regulations / Medical Device Distribution / Dublin / Ireland

 

Job Title: Regulatory Affairs Specialist (12 Month Project Manager)

Reports To: QCRA Manager

Location: Dublin Head Office

Package:

  • 12 Month Contract
  • € – Dependent on Experience and open to Negotiation
  • Parking
  • Travel Allowance
  • Paid Annual Leave

 

Role:

Project Management:

  • Lead the planning and implementation of the EUDR project in conjunction with key stakeholders
  • Play a leading role in defining project scope, goals and deliverables
  • Define the required resources to meet project goals
  • Ensure momentum of each work-stream by engaging with relevant stakeholders to keep actions on track and to document project progress
  • Scheduling stakeholder meetings with relevant teams for each individual work-stream, diary scheduling and room bookings
  • Identification and recording of potential blocks/obstacles to the project, identify and propose solutions
  • Driving risk mitigation plans across each work-stream
  • Documenting actions required and completed and updating each team on progress
  • Administration of project documentation including planning documents, risk registers, action logs, stakeholder update

 

Stakeholder Management:

  • Present to Project Steering Group on a monthly basis – including progress, plans, problems and solutions
  • Reporting updates to the QCRA manager and stakeholders on a weekly basis
  • Implement and manage change when necessary to meet project outputs
  • Evaluate and assess result of project

 

Experience:

 

  • Third Level Qualification / Degree in Quality, Science or Business
  • 2 – 3 Years’ experience in Medical Device Regulatory Affairs
  • Full Clean Driving License required

 

If you would like to be considered for this fantastic opportunity why not contact me directly on my mobile 00353 (0) 87 25 35 247; Just ask for Patrick.

 

Alternatively, follow the links below and send me your CV.

 

Key Words: Regulatory Affairs Specialist / Regulatory Affairs Advisor / Regulatory Affairs Officer / RA Specialist / Medical Device Regulations / Medical Device Distribution / Dublin / Ireland

 

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To apply for this job please visit independentsearchsolutions.com.