Regulatory Affairs Specialist

About the RolePale Blue Dot Recruitment is seeking a Senior Regulatory Affairs Specialist to join their team. As a key member of the regulatory affairs department, you will be responsible for developing and implementing regulatory strategies to support the timely and successful registration, approval, and maintenance of company and client products.Key...

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 Description:The Senior Regulatory Scientist role is a critical position in the regulatory affairs team, responsible for assisting in the running of regulatory programmes and providing input into regulatory strategies.Key responsibilities include implementing regulatory requirements, maintaining an excellent understanding of global medical device...

OverviewCook Medical is a leading medical device company that develops and manufactures innovative products to improve patient outcomes. We are seeking a highly skilled Regulatory Affairs Expert to join our team.

We're looking for people who are determined to make life better for people around the world. Organization Overview: At Lilly, we serve an extraordinary purpose. We make a difference for people around the globe by discovering, developing and delivering medicines that help them live longer, healthier, more active lives. Not only do we deliver...

OverviewThe Regulatory Scientist 2 will be involved in the development and generation of post market surveillance (PMS) plans and reports for Cook Ireland medical devices. In addition, the Regulatory Affairs Specialist will perform activities associated with PMS, including Post Market Clinical Follow-Up (PMCF), and Clinical Evaluation Plans and Reports...

Overview The primary role of the Senior Regulatory Scientist is to assist in the running of the regulatory affairs by providing input into: regulatory strategies, performing activities associated with obtaining and maintaining regulatory approval to commercialise medical devices in selected target markets and providing regulatory affairs input for the...

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

Job SummaryPale Blue Dot Recruitment is seeking a highly skilled Senior Regulatory Affairs Specialist to join their team. In this role, you will be responsible for developing and implementing regulatory strategies to support the successful registration, approval, and maintenance of company and client products.Main ResponsibilitiesDevelop and implement...

Role Summary:This is an exciting opportunity for a highly skilled and experienced professional to join our regulatory affairs team as a Senior Regulatory Scientist.The successful candidate will be responsible for assisting in the running of regulatory programmes, providing input into regulatory strategies, and ensuring compliance with relevant ISO, EU, and...

Job DescriptionMaintain an excellent understanding of global medical device regulations for specific jurisdictions as assigned.Develop global regulatory strategies for Cook medical devices in collaboration with other regulatory affairs or clinical personnel.Communicate country/region specific regulatory requirements to the regulatory...

We're recruiting for a Regulatory Compliance Specialist to join our Medical Device organization based in Limerick. This is an excellent opportunity for anyone who is passionate about regulatory compliance.About the RoleAs a Regulatory Compliance Specialist, you will be responsible for ensuring that our products meet the highest standards of quality and...

Work Flexibility: Onsite This position provides experience of working in a regulated medical device company. You will have the opportunity to develop and apply basic knowledge and understanding of the quality, regulatory and legal frameworks, regulatory requirements, legislation, processes and procedures.  Additionally, this opportunity provides good...

About the Role:We are looking for a highly motivated and experienced Regulatory Compliance Specialist to join our team at Regeneron Ireland DAC. As a QA Specialist, you will be responsible for ensuring the quality and compliance of our biologics manufacturing operations.Key Responsibilities:Preparation and review of batch disposition documentation to support...

About Our Commitment to Diversity and InclusionWe are committed to fostering a culture of diversity and inclusion, where everyone feels valued, respected, and empowered to contribute their best work.We believe that a diverse and inclusive workplace is essential to driving innovation, collaboration, and excellence.About This RoleWe are seeking a highly...

We are seeking a Regulatory Compliance Specialist to join our quality assurance team at TN Ireland. As a member of our team, you will play a critical role in maintaining the highest standards of product quality and compliance for our computer systems.Key Responsibilities:Regulatory Compliance:Stay current with industry regulations, guidelines, and best...

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...

**About the Role:**Northern Trust is a globally recognized, award-winning financial institution that has been in continuous operation since 1889. We are seeking an experienced AML Remediation Specialist to join our Global Regulatory Affairs Office.The successful candidate will report to the Remediation Validation Testing Manager and will bring proven...

About the OpportunityWe are seeking a highly skilled Senior Regulatory Affairs Specialist to join our team. In this role, you will be responsible for developing and implementing regulatory strategies to support the successful registration, approval, and maintenance of company and client products.Key AccountabilitiesDevelop and implement regulatory strategies...

Key ResponsibilitiesLead business analysis activities within the Cyber and Regulatory Remediation Programme, focusing on cyber security requirements and compliance.Work closely with stakeholders to gather and document detailed business and technical requirements related to cyber security, compliance, and third-party risk.Provide expert advice on cyber risk...