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Life Science

Websitehttp://lifescience.ie Phone Number:(01) 685 45 45
Email:info@lifescience.ie Map:Click here


Life ScienceRecruitment is a specialist science recruitment agency with a specific focus on the recruitment and selection of professionals for the pharmaceutical, biotechnology, healthcare, clinical research, medical device, engineering and scientific sectors in Ireland. Whether its science jobs, pharmaceutical jobs, biotechnology jobs or a job in clinical research you're looking for, our consultants are industry professionals strategically placed in the best position possible to help you achieve your dream position.


At Life Science Recruitment we understand your needs and are committed to helping you to move forward in your career. Our philosophy is simple; life scientists recruit life scientists, chemists recruit chemists etc. - you know you are speaking to a peer who understands where you're coming from and can advise on the best route forward in your new career.

Life Science Recruitment's mission is to bring specialist recruitment to the next level, with a fresh novel outlook combined with creative thinking to provide the best possible quality of service and standards in Irish recruitment

Life Science has the following jobs posted
Job Title. Location Salary Actions

Regulatory Affairs & Communications Specialist

The Regulatory Affairs Specialist - Regulatory Communications serves as a communication liaison between the manufacturer and the local affiliates or regulatory authorities and assists in assessing complaints for Regulatory Reporting, this includes Adverse Event Reporting (MDR, Vigilance, etc.), Post Market Surveillance Activities (PMS, PMCF, CER) and associated correspondence to applicable Regulatory bodies. Reporting to: Senior Regulatory Affairs Specialist, you will: • Assess complaints from global distribution centres for adequate information to det...

Location: Limerick,
Regulatory Affairs & Communications Specialist 		Limerick Not Disclosed

Lab Technician

We’re currently recruiting for an exciting opportunity with an award-winning medical device organization based in Galway. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do. Duties You will be part of a high performing Complaint Handling and Medical Device Regulatory reporting department, which provides value throughout the Product Life cycle through world class execution in Medical Device Reporting and Vigilance compliance. Responsibilities may include the follow...

Location: Galway,
Lab Technician 		Galway Not Disclosed

German Speaking Medical Information Analyst

German Speaking Medical Information Analyst Our Cork based client are currently recruiting for a German Speaking Medical Information Analyst to join their team on a permanent basis. As Medical Information Analyst you will be required to provide excellent and efficient Medical Information support to Healthcare professionals, patients and other customers & to complete the relevant documentation for these queries. Responsibilities • Manage customer queries regarding products/medical devices from healthcare professionals, patients and other customers in a courteous...

Location: Cork,
German Speaking Medical Information Analyst 		Cork Not Disclosed

Communications Specialist

Communications Specialist Our client, a Global pharmaceutical organisation are currently recruiting for a number of Communication Specialists to join a new team in the organisation. As communication specialist you will handle customer interactions including calls and alternate channels (e.g. emails, chats, etc.), analyses customers’ questions to formulate an accurate and complete response using approved resources in a timely manner & ensures best in class customer service at all times Responsibilities • Maintain and demonstrate product and proce...

Location: Cork,
Communications Specialist 		Cork Not Disclosed

Regulatory Affairs Specialist

Our client a medical device early stage company wishes to add a Regulatory Affairs Specialist to our team. The successful candidate will work with the Design, Quality and Regulatory teams to support all regulatory functions for both existing and new products. Role/Responsibilities • Contribute to the regulatory strategy plans for new products, including required Regulatory Agency approvals. • Provide regulatory input into labelling, test strategies for new product development, risk analysis, clinical, preclinical and marketing issues. • Planning,...

Location: Cork,
Regulatory Affairs Specialist 		Cork Not Disclosed

Regulatory Affairs Manager

Regulatory Affairs Manager Our client a medical devcie multinational currently seeks a Reg Affairs Manager to join their team. Reporting to Senior Director QA/RA the Reg Affairs manager will support the Strategic Manufacturing group to prepare global submission and registration documents in support product transfer activities; complete risk management activities, transfer and maintain technical files/design dossiers for the transfer products. The candidate is required to work effectively with cross-functional groups and global regulatory affairs contacts to maintain worldwide Regul...

Location: Westmeath,
Regulatory Affairs Manager 		Westmeath Not Disclosed

Regulatory Affairs Officer

Regulatory Affairs Officer This company are exclusively sourcing a Regulatory Affairs Officer based in Limerick. The ideal candidate will have a degree in molecular science with the ability and confidence to undertake all associated responsibilities. This role will also involve R&D Liaison with R&D teams. Roles & Responsibilities Coordination of post market surveillance/vigilance reporting for CE-IVD marked products. Coordination of risk management activities and documentation for CE-IVD marked products. Communication of specific regulatory requir...

Location: Limerick,
Regulatory Affairs Officer 		Limerick Not Disclosed

Regulatory Affairs Specialist

This job requires the person to work within the current regulatory environment and frameworks for all relevant markets. You will support marketing the products and ensure they are in conjunction with the commercial requirements. Duties/Responsibilities: • Define regulatory strategy for individual devices within the Product Development Process. • As appropriate, manage Submissions and Significant Changes and Notified Body interactions. • Assist with the preparation of egulatory filings and subsequent FDA correspondence on submissions. • Manage R...

Location: Galway,
Regulatory Affairs Specialist 		Galway Not Disclosed

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,
Regulatory Affairs & Quality Manager 		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

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,
Head of Quality & Regulatory Affairs 		Dublin Not Disclosed
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