Hot Medical Affairs Jobs

Vigilance Assessor

Reporting to the Director of Human Products Monitoring the role of the Vigilance Assessor is to provide post marketing evaluation and regulation of the benefits and risks of medicinal products in Ireland and the European Union and to provide technical support to the Director of Human Products Monitoring in order to facilitate the effective safety monitoring of medicinal products. A degree in Pharmacy or a PhD with 3 years research experience is essential for this role. Role/Responsibilities: o Signal detection activities using available databases and with integration of quantitative ...

Location: Dublin,

Regulatory Affairs & Quality Manager

Regulatory Affairs & Quality Manager Our client a cardiovascular medical device start-up looking to hire a Quality and Regulatory Affairs manager. The succ

Location: Dublin,

Fluent French Senior Medical Information Analyst

Fluent French Senior Medical Information Analyst Our client, a global pharmaceutical organisation are currently recruiting for a Senior Medical Information Analyst to join their team on a permanent basis. As Senior Medical Information Analyst you will provide accurate & efficient Medical Information support to Healthcare professionals, patients and other customers. You must be a fluent French speaker to apply for this opportunity. Responsibilities • Manage customer queries regarding products & medical devices from healthcare professionals, patients and...

Location: Cork,

Sales & Applications Specialist

Our client is a leading distributer of Life Science solutions to Healthcare, Academia & Industrial markets. They are currently seeking a Life Science Sales & Applications Specialist who will represent and sell products which are part of a diverse and extensive line of Life Science reagents, consumables and instrumentation. The successful candidate will manage and grow new business relationships within academic, biotech, food and pharma accounts. This includes working existing accounts as well as prospecting for new customers, qualifying leads and training customer...

Location: Dublin,

Regulatory Affairs Associate

Regulatory Affairs Associate Our client is looking for a regulatory affairs associate who will deal with the compliance and approval of products. This person will also be responsible for determining and supporting regulatory activities. Responsibilities • Use technical solutions for problem solving • Improve quality of projects • Use strong writing skills to clearly define and describe technical information • Analyse customer complaints • Identify trends and corrective actions • Review and assess of change control activities for po...

Location: Westmeath,

Consultant

Life Science Recruitment is a specialist recruitment agency with a focus on the recruitment and selection of professionals for the pharmaceutical, biotechnology

Location: Cork,

QA Specialist (QC)

This position is responsible for carrying out tasks and projects related to management of Quality Assurance activities at Janssen Biologics as required by Good Manufacturing Practice (GMP). These activities include Incoming material release, Batch release, Change control, Event management, Supplier qualification, Annual product review and Validation compliance activities.Provide support and direction to all departments in respect of specific quality system elements to ensure business, quality and compliance goals are met. GENERAL SCOPE OF RESPONSIBILIT...

Location: Cork,

Head of Quality & Regulatory Affairs

Head of Quality & Regulatory Affairs Our client a multinational healthcare company currently seeks Head of Quality and Regulatory Affairs. Reporting to Ge

Location: Dublin,