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Search Results for Regulatory Affairs for Regulatory Affairs
Job Title. | Location | Salary | Actions |
Blood Tissue and Organ InspectorBlood Tissue and Organ Inspector Our client, a large regulatory body, are currently recruiting for a Blood Tissue and Organ Inspector to join their team. As Blood Tissue and Organ Inspector you will be responsible for assessing the compliance of organ procurement centres, organ transplant centres, blood establishments and tissue establishments with the requirements of European and National legislation and associated good practice guidelines. The role of an Inspector is to evaluate the compliance of sites inspected, in Ireland and abroad, with the requirements of National legi...Location: Dublin, |
Dublin | 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 | |
CMC Pre-Approval Regulatory ScientistCMC Pre-Approval Regulatory Scientist Our client, a global pharma company, are currently recruiting for a CMC Pre-Approval Regulatory Scientist to join their team on a permanent basis. This is an excellent opportunity to join a global team very strong of regulatory experts.. As CMC Pre-Approval Regulatory Scientist, you will partner with Global Regulatory Affairs – CMC (GRA-CMC) Regulatory Scientists to provide strategic, tactical and operational direction and support to expedite CMC development of the organisations portfolio by developing successful regul...Location: Cork, |
Cork | Not Disclosed | |
Principal Scientist Global Regulatory Affairs CMCPrincipal Scientist- Global Regulatory Affairs-CMC Our client, a global pharma company, are currently developing a state-of-the-art biotech manufacturing facility based in Limerick (hybrid working) and are currently recruiting for a Principal Scientist- Global Regulatory Affairs-CMC to join their team on a permanent basis. As Principal Scientist- Global Regulatory Affairs-CMC you will provide strategic, tactical and operational direction to expedite the CMC development of the organisations portfolio and technical agenda by supporting global clinical trial, market registration...Location: Limerick, |
Limerick | Not Disclosed | |
Regulatory Affairs ManagerRegulatory Affairs Manager Our client, a pharma organisation, are currently recruiting for a Regulatory Affairs Manager to join their team on a permanent basis with hybrid working. Experience working with oral solid dosage (OSD) forms is essential for this role. You will work with a small team in Ireland and other team members across the UK and EU. Responsibilities Advise and liaise services on behalf of company to ensure that requirements of national competent authorities are met Create, assemble, review and publish regulatory submissions in accordance with agreed ...Location: Dublin, |
Dublin | Not Disclosed | |
CMC Regulatory Principal ScientistCMC Regulatory Principal Scientist Our client, a global pharma company, are currently recruiting for a CMC Regulatory Principal Scientist to join their team on a permanent basis. This is an excellent opportunity to join a global team very strong of regulatory experts. This role offers hybrid working. As CMC Regulatory Principal Scientist, you will lead various aspects of the global marketing authorization submission management processes, help manage submission content for Drug Substance and Drug Product, provide guidance on structure and content placement within CTD registration...Location: Cork, |
Cork | Not Disclosed | |
CMC Regulatory Senior ScientistCMC Regulatory Senior Scientist Our client, a global pharma company, are currently recruiting for a CMC Regulatory Senior Scientist to join their team on a permanent basis. This is an excellent opportunity to join a global team very strong of regulatory experts. This role offers hybrid working. As CMC Regulatory Senior Scientist, you will lead various aspects of the global marketing authorization submission management processes, help manage submission content for Drug Substance and Drug Product, provide guidance on structure and content placement within CTD registration submissi...Location: Cork, |
Cork | Not Disclosed | |
Regulatory Affairs - Complaints Co-OrdinatorAMC0010 Regulatory Affairs - Complaint Co-ordinator 6 month contract Hybrid - Dublin - D12 Product Complaints Coordinator Role Main tasks: Management of product complaints for products on the Irish market, from initial receipt through to closure, in conjunction with the company’s Global Complaints Departments and in accordance with all relevant EU legislation, HPRA Guidelines and company specific Standard Operating Procedures. Document and maintain the complaint files for reports received. Prompt communicati...Location: Dublin, |
Dublin | 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 | |
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 | |
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 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 |
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Pharmaceutical | Tel:+353 1 685 4545 | Fax: +353 (0)1 443 05 24 | Email: [email protected] | Copyright © 2012 Life Science Recruitment Ltd
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Pharmaceutical | Tel:+353 1 685 4545 | Fax: +353 (0)1 443 05 24 | Email: [email protected] | Copyright © 2012 Life Science Recruitment Ltd
This site uses cookies. For more information on our cookie policy visit Privacy Policy | Terms of Use
Registered as a private limited company. No: 445328 |
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