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Search Results for Scientific
Job Title. Location Salary Actions

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,
Vigilance Assessor 		Dublin Not Disclosed

GMP Inspector

GMP Inspector Reporting to a GMP Inspection Manager, the GMP Inspector will be responsible for assessing the compliance of manufacturers with EU Good Manufacturing Practice (GMP). The Manufacturing Compliance Specialist will evaluate the compliance of sites inspected, in Ireland and abroad, with the requirements of National legislation European Community Directives, Regulations and Guidance. These sites may include; • Manufacturers and distributors of medicinal products. • Manufacturers of investigational medicinal products. • Sites involved in ...

Location: Dublin,
GMP Inspector 		Dublin Not Disclosed

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,
Regulatory Affairs Associate 		Westmeath Not Disclosed

Quality Assurance and Regulatory Affairs Manager

Quality Assurance and Regulatory Affairs Manager Our client, one of the largest biomedical innovator based in Dublin is looking to recruit QA/RA Manager wh

Location: Dublin North,
Quality Assurance and Regulatory Affairs Manager 		Dublin North Not Disclosed

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,
Consultant 		Cork Not Disclosed

Mechanical Design Engineer

Mechanical Design Engineer required to focus on the development of cutting edge medical devices in the Cardiac and Vascular space. Engineers are directly involved in the development of innovative products for use in medical procedures. Principal R&D Engineers are directly involved in all stages of the product development process from concept generation through to commercialization of cutting edge devices such as structural heart devices. Responsibilities: Support basic clinical need through opportunity assessment and device concept to prototype. You will participate in...

Location: Galway,
Mechanical Design Engineer 		Galway Not Disclosed

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,
QA Specialist (QC) 		Cork Not Disclosed

Associate Scientist

Life Science Recruitment Cork are currently recruiting a Scientist for a large multinational client in Cork where they will be responsible for Tox Release testing, Clinical Release and Stability testing for Drug Substance and Drug Product, and Stability Lifecycle management.The Clinical Release & Stability Department in Cork, Ireland, is responsible for the biotechnology (Large molecule) scope of the PDMS product portfolio. Education and Experience/Competencies A minimum of Degree in Chemistry, Biochemistry, Pharmaceutical Sciences or ...

Location: Cork,
Associate Scientist 		Cork €40000 - €45000
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