Post Market Surveillance & Clinical Spe

CPL

Limerick

On behalf of my client, a global medical device company, I am recruiting for a Post Market Surveillance & Clinical Specialist. In this role you will join the Regulatory Affairs team and you will be involved in the development and generation of post market surveillance (PMS) plans and reports for my Clients medical device portfolio in Ireland. In addition, you will perform activities associated with PMS, including Post Market Clinical Follow-Up (PMCF), and Clinical Evaluation Plans and Reports (CEPs, CERs. Applications are invited from candidates with the following background and experience: Third level Qualification in any of the following areas: Science/Engineering, Pharmacy, Medicine, Nursing desired. 2 years experience in a regulated industry in a similar role would be advantageous. Knowledge of regulations pertaining to PMS, PMCF and CERs particularly in relation to the EU (MDD & MDR regulations) would be advantageous. Knowledge of medical device quality standards/practises or similar regulated industry knowledge. Good communication and inter-personal skills with ability to communicate clearly and concisely in both spoken and written form. Participate in a team-based environment. Proven problem-solving skills. Good technical writing skills; advantageous to have experience in medical writing. Knowledge / use of search databases for published literature (Embase, MEDLINE etc.) Good computer skills including knowledge of Microsoft. Proven organisational skills. High level of self-motivation. Willingness and availability to travel on company business as required. For a full Job Spec and to apply for this position please call me on +353 1 2784671 or e-mail dbolger@thornshaw.com. Thornshaw Scientific Recruitment is a leading Irish provider of specialist Scientific Recruitment. Part of the CPL Group. www.thornshaw.com Tel: +353 1 2784671. This job originally appeared on RecruitIreland.com.

1780 days ago