Regulatory Documentation Specialist

At TN Ireland, we're seeking a highly skilled Documentation Specialist to join our Engineering team. As a key member of our documentation team, you'll be responsible for creating technical documents that support the Engineering department.Job Responsibilities:Create and submit high-quality technical documents such as Change controls, risk assessments, and...

TN Ireland is seeking a skilled GMP Documentation Specialist to create high-quality documentation for a major expansion project.Job Description:Responsibilities include developing and reviewing GMP documentation, including SOPs, training materials, and calibration records.Close collaboration with cross-functional teams ensures that all documentation meets...

We are seeking a skilled Document Control Specialist to join our team at Global Professional Consultants. As a key member of the project team, you will be responsible for managing and maintaining accurate and up-to-date documents, ensuring compliance with regulatory requirements.In this role, you will work closely with the project manager and quantity...

Job DescriptionWe are seeking a skilled Document Controllers Specialist to join our team at TN Ireland.The successful candidate will be responsible for managing electronic documentation and records across various systems, ensuring compliance with global and local requirements. This role requires strong organizational and analytical skills, as well as the...

Job SummaryTN Ireland is seeking a highly skilled Regulatory Writer to join our team.This role involves creating high-quality regulatory documents, including GMP documents, labeling, and packaging information.You will work closely with regulatory affairs specialists to develop and maintain accurate and up-to-date content.Strong knowledge of regulatory...

We're looking for a skilled and experienced Regulatory Compliance Specialist to join our quality assurance team at Eli Lilly Limerick. As a Senior Qualified Person, you'll be responsible for ensuring the quality and regulatory compliance of our biopharmaceutical products within our next-generation manufacturing facility.This role requires a deep...

Job OverviewTN Ireland is seeking a highly skilled Documentation Specialist to join our team.The successful candidate will be responsible for creating high-quality GMP documents, including standard operating procedures, system design documents, and work instructions. This role requires strong collaboration with subject matter experts and key functional...

About Us:Northern Trust is a leading financial institution that provides innovative services and guidance to the world's most successful individuals, families, and institutions. Our company has been in continuous operation since 1889 and has a strong commitment to service, expertise, and integrity.We have a globally recognized team of professionals who...

Social network you want to login/join with:Technical Regulatory Specialist, LimerickClient:Northern Trust CorporationLocation:Limerick, IrelandJob Category:OtherEU work permit required:YesJob Reference:b1139177ffa8Job Views:87Posted:21.01.2025Expiry Date:07.03.2025Job Description:About Northern Trust:Northern Trust, a Fortune 500 company, is a globally...

OverviewThe Regulatory Affairs Specialist 2 plays a crucial role in developing regulatory strategies to secure approval for medical devices in target markets. This specialist serves as a liaison between the manufacturer and local affiliates, distribution partners, or regulatory authorities. Reporting directly to the Team Lead, Regulatory Affairs or Manager,...

Role Overview:We are seeking a highly skilled and experienced Technical Regulatory Specialist to join our Regulatory Risk & Oversight Office in Asset Servicing. The successful candidate will play a key part in shaping our regulatory approach and ensuring compliance with relevant regulations.The Technical Regulatory Specialist will work closely with our...

Overview The Regulatory Affairs Specialist 2 ensures regulatory compliance to the EU MDR at the office of the EU Authorised representative (AR).The EU AR Office is responsible for verifying compliance to the EU MDR on behalf of Cook Medical's non-EU manufacturers.The Regulatory Affairs Specialist 2 serves as a communication liaison between the Cook...

Social network you want to login/join with:Regulatory Affairs Specialist 2 (Hybrid), LimerickClient:Cook MedicalLocation:Limerick, IrelandJob Category:OtherEU work permit required:YesJob Reference:5c63328c9fe6Job Views:65Posted:22.01.2025Job Description:OverviewThe Regulatory Affairs Specialist 2 ensures regulatory compliance to the EU MDR at the office of...

About Northern Trust: Northern Trust, a Fortune 500 company, is a globally recognized, award-winning financial institution that has been in continuous operation since 1889. Northern Trust is proud to provide innovative financial services and guidance to the world's most successful individuals, families, and institutions by remaining true to our enduring...

Overview The Regulatory Affairs Specialist 2 ensures regulatory compliance to the EU MDR at the office of the EU Authorised representative (AR). The EU AR Office is responsible for verifying compliance to the EU MDR on behalf of Cook Medical's non-EU manufacturers. The Regulatory Affairs Specialist 2 serves as a communication liaison between the Cook...

Job DescriptionCPL is seeking a highly organized and detail-oriented Technical Document Specialist to join their team. In this role, you will be responsible for managing, organizing, and maintaining all project-related documents throughout the lifecycle of a project.The successful candidate will have excellent attention to detail, strong organizational...

OverviewThe Regulatory Affairs Specialist 2 helps develop regulatory strategies and performs activities associated with obtaining and maintaining regulatory approval to commercialize medical devices in selected target markets. The Regulatory Affairs Specialist 2 serves as a communication liaison between the Cook manufacturer and the Cook local affiliates,...

Overview The Regulatory Affairs Specialist 2 helps develop regulatory strategies, performs activities associated with obtaining and maintaining regulatory approval to commercialise medical devices in selected target markets. The Regulatory Affairs Specialist 2 serves as a communication liaison between the Cook manufacturer and the Cook local affiliates,...

Job Description:The Regulatory Affairs Specialist 2 at Cook Medical plays a crucial role in developing and implementing regulatory strategies for medical devices. This position requires a deep understanding of global regulations, including ISO 13485, MDD 93/42/EEC, EU Medical Device Regulation 2017/745, and FDA QSP 21 CFR Part 820.Responsibilities:Maintain...

Role DescriptionNorthern Trust is a forward-thinking company that prides itself on its commitment to compliance and regulatory risk management. We are seeking a highly skilled Regulatory Compliance Specialist to join our team in Limerick, Ireland.About the RoleThe successful candidate will be responsible for executing the testing program, independently...