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Life Science
Website | http://lifescience.ie | Phone Number: | (01) 685 45 45 |
Email: | [email protected] | 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.
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
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.
Job Title. | Location | Salary | Actions |
Associate Director (Quality Assurance) - LimerickAssociate Director (Quality Assurance) Our client, a global biotech, are currently recruiting for an Associate Director Quality Assurance to join their team on a permanent basis. As Associate Director Quality Assurance, you will lead the cross functional support of the manufacturing , warehouse and/or quality control operations. You will be responsible for QA business processes including support of GMP and GLP compliance, regulatory inspection readiness, Quality Plan and continuous improvement projects and will provide leadership and direction to the QA team. Respon...Location: Limerick, |
Limerick | Not Disclosed | |
Associate / Sr Associate (Regulatory Labelling)Associate / Sr Associate - Regulatory Labelling Our client is a global healthcare leader. Their employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. They are looking for people who are determined to make life better for people around the world. For more than 140 years, they have worked tirelessly to discover medicines that make life better. They are currently seeking a Labelling Associate / Senior Labeling...Location: Cork, |
Cork | Not Disclosed | |
Senior Reg Affairs Specialist - Post MarketJob title: Senior Regulatory Affairs Specialist – Post market Location: Parkmore, Galway. 1-2 days a week on site Benefits: Top salary, Bonus, pension, healthcare, hybrid working Overview: My client are a fast-paced, rapidly growing medical device company offering a highly differentiated solution in vascular interventions. With a culture of innovation helping each individual develop both professionally and personally, and our culture of respect means that they all work in a collaborative, empowering, and exciting environment. Reporting to t...Location: Galway, Galway City, |
Galway | Not Disclosed | |
Design Assurance EngineerJob title : Design Assurance Engineer Location: Galway West Business Park Benefits: Competitive salary, Share options, excellent opportunity to develop your experience and career in an exciting start up helping develop a product from its very early stages. Company: My client an early-stage medical device start-up company focused on the design and development of novel devices for the treatment of Intracranial Atherosclerotic Disease. This is a new and evolving treatment area likely to be the next frontier in Neuro-intervention. Overview: ...Location: Galway, Galway City, |
Galway | Not Disclosed | |
Qualified PersonQualified Person Our client, a global biotech,are seeking a highly motivated and detail-oriented Qualified Person to join the quality assurance team as the Lead QP onsite. The successful candidate will have previously been a named QP on a Irish licence previously. Responsibilities Ensure manufactured biotech drug substance (DS) batches are certified in accordance with all required regulations and in compliance with IND/CTAs/ manufacturing authorisation/ marketing authorisation Ensure that biotech drug product batches are test...Location: Limerick, Limerick City, |
Limerick | Not Disclosed | |
Senior Regulatory Affairs SpecialistJob title: Senior Regulatory Affairs Specialist – Premarket Location: Parkmore, Galway. 1-2 days a week on site Benefits: Top salary, Bonus, pension, healthcare, hybrid working Company: My client are a fast-paced, rapidly growing medical device company offering a highly differentiated solution in vascular interventions. This role is best suited to an individual who is self-motivated, accountable and seeking infinite learning and growth opportunities. Role: As a Senior Regulatory Affairs Specialist you will will pl...Location: Clare, Connaught, Galway, Galway City, Limerick, |
EU | Not Disclosed | |
Quality Systems EnginerRole: Quality Systems Engineer 24 month ftc with strong chance of going permanent. Based in Dun Laoghaire – on site role Competitive salary, Healthcare, bonus or share options. Pension contribution from company after 24 months. Job Purpose: Reporting to the Quality Systems Manager, duties will include implementing & maintaining the Company’s Quality Management System in accordance with applicable standards and regulations Responsibilities: Be a key driver of cGMP practices within Operations and Quality divisions Act as a p...Location: Dublin, Dublin City Centre, Dublin Greater, Dublin North, Dublin South, |
EU | Not Disclosed | |
Manufacturing EngineerMy Client: My client are based in Bishopstown, Cork and have developed a breakthrough single-use medical device, Solo+ TTD that addresses pain points of the current treatment of the surgical tympanostomy, a procedure that drains out the excess fluid built up in the ear. The surgical tympanostomy is the most common procedure done on children. This company was crowned Seedcorn’s Overall Winner for the Best Early Stage Company in 2014 and Emerging Medtech Company of the Year, Irish Medical Device Association (IMDA) in 2015. The AventaMed team have successfully co...Location: Cork, |
Cork | Not Disclosed | |
Quality ManagerJob title: Quality Engineer/ Quality Manager Location: ATU Ihub, Galway Company: My client are a developer of innovative medical devices which transform the mobility and quality of life of enteral feeding users. Their team understands that current feeding systems are complex, inconvenient and a burden on users’ daily lives. My client have developed the Mobility+® the first of its kind FDA cleared Elastomeric enteral feeding system. The Mobility+® is now available in the US market and has FDA Approval. Overview: As a Quality Engi...Location: Clare, Galway, Galway City, Limerick, Limerick City, |
EU | Not Disclosed | |
Quality EngineerRole: Quality Engineer Location: Mullingar, Westmeath (On site) Benefits: Good salary, pension, healthcare and yearly bonus. Company: My client are an exciting business located in a modern state of the art facility in Mullingar Co. Westmeath. Passionate about serving the world’s medical device and allied healthcare industries in offering a range of the highest quality innovative healthcare packaging solutions. Role: Reporting to the Senior Quality engineer and/or Quality and Regulatory Director the Quality Engineer will work in collaboration with the s...Location: Athlone, Cavan, Dublin, Kildare, Longford, |
EU | Not Disclosed | |
Quality Systems ManagerCompany: My client are have a global portfolio which includes best-in-class, iconic brand-name products as well as global key brands; generics, including branded and complex generics; and other offerings across a wide range of therapeutic areas. They are committed to helping create healthier communities worldwide through education, outreach and better access to treatment Role: Quality Systems Manager - Senior Location: Newenham Court, Northern Cross, Malahide rd, Dublin 17 Team: 6 direct reports Hybrid working: 2-3 days a week on site per week Benefits: Compe...Location: Dublin, Dublin City Centre, Dublin Greater, Dublin North, Dublin South, |
EU | Not Disclosed | |
Quality EngineerRole: Quality Engineer Location: Mullingar, Westmeath (On site) Benefits: Good salary, pension, healthcare and yearly bonus. Company: My client are an exciting business located in a modern state of the art facility in Mullingar Co. Westmeath. Passionate about serving the world’s medical device and allied healthcare industries in offering a range of the highest quality innovative healthcare packaging solutions. Role: Reporting to the Senior Quality engineer and/or Quality and Regulatory Director the Quality Engineer will work in collaboration with the s...Location: Athlone, Cavan, Dublin, Kildare, Longford, |
EU | Not Disclosed | |
Senior Regulatroy Affairs SpecialsitSenior Regulatory Specialist Our client a well funded high potential medical device start up are currently seeking experienced regulatory professional top join their team. The Senior Regulatory Affairs Specialist will work closely with a cross-functional team to obtain the regulatory approvals/clearances needed to support clinical and commercial use of an innovative new therapy. Role/Responsibilities Support and advise the VP Quality and Regulatory Affairs by executing regulatory activities and developing regulatory strategies to support...Location: Galway, |
Galway | Not Disclosed | |
Medical Device DirectorOur client a Medical Devcie notifeid body are currently seeking Director of Medical Devices to join their team. The Director of Medical Devices will have overall leadership repsonsibility for European and US Medical Division and provide leadership and strategic guidance. Role can be based in Dublin or Galway and can provide hybrid Roles/Responsibilities Responsible for European and US Medical Device Division Manage resources for Global Medical Device division Responsible for department KPIs and all certifications filed Oversee global audit team planning Mem...Location: Republic of Ireland, |
Republic of Ireland | Not Disclosed | |
Regulatory Affairs SpecialistRegulatory Affairs Specialist (Remote/Hybrid) Our client a high potential start up medical device company currently seeks a Regulatory Affairs Specialist to join their team. Reporting to the Clinical and Regulatory Affairs Manager, the Regulatory Specialist will be responsible for helping with compliance to standards, regulatory submissions and annual reporting to the notified body and FDA. The Regulatory Affairs Specialist must have a working knowledge of medical device regulatory requirements and standard practices in the medical device industry. This position re...Location: Cork, |
Cork | Not Disclosed | |
Senior Regulatory AffairsOur client a growing medical device organisation currently seeks a Senior Regulatory Affairs Specialist to join their team. The Senior Regulatory Affairs Specialist will be responsible for all regulatory activities including product certification and compliance, and for supporting the ongoing maintenance, audit and continuous improvement of specific elements of the Quality Management System Role/Responsibilities Manage the regulatory and vigilance process. Prepare regulatory submissions for required markets coordinating input from other stakeholders, tr...Location: Galway, |
Galway | Not Disclosed | |
Senior Regulatory Affairs SpecialistSenior Regulatory Affairs Specialist Our client a Medical Device Multinational currently seeks a Senior Regulatory Specialist to join their team. The Senior. Regulatory Affairs Specialist will develop strategies and submissions for complex projects and issues related to regulatory documents, submissions, investigations, product development planning and regulatory agency interaction. The Sr. Regulatory position will assist in mentoring and development of staff members as part of the role. Role/Responsibilities • Manage Technical Documentation ...Location: Westmeath, |
Westmeath | Not Disclosed | |
Senior Regulatory Affairs SpecialistSenior Regulatory Affairs Specialist Our client a high potential medical device start up current seeks a Senior Regulatroy Affairs Specialist to join their team. Reporting to the Director of Quality and Regulatory Affairs the Senior Regulatory Affairs will take an active role in developing the Regulatory strategy in Europe and the US and interacting with the relevant Regulatory and Notified Bodies. They will also be required to help maintain the Design History Fileof Class III implant. This position offers the opportunity to join in an exciting early stage company developing a...Location: Dublin, |
Dublin | Not Disclosed |
Regulatory Affairs | Tel:+353 1 685 4848 | Fax: +353 (0)1 443 05 24 | Email: [email protected]
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