Regulatory Affairs Manager for Medical Devices

Senior Manager Regulatory Affairs for Medical Devices and Person ResponsibleVectura Ireland Limited is seeking a Senior Manager in Regulatory Affairs for Medical Devices who will also assume the critical role of Person Responsible for Regulatory Compliance (PRRC). This position plays a key role in ensuring compliance with European medical device regulations...

VisionWe are seeking an experienced Senior Manager in Regulatory Affairs for Medical Devices to join our team at Vectura Group plc. As Person Responsible for Regulatory Compliance (PRRC), you will play a critical role in ensuring compliance with European medical device regulations. Your expertise will contribute to the success of our global regulatory...

Social network you want to login/join with:Have you ever wanted to make a difference?At Abbott, you will play a crucial role to help people live more fully at all stages of their lives. Abbott is a global healthcare leader and our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics,...

Job DescriptionKey Responsibilities:Ensure full compliance with European medical device regulations in your capacity as Person Responsible for Regulatory Compliance (PRRC)Lead communications and interactions with Competent Authorities regarding Vectura's duties as Authorized RepresentativeContribute to global regulatory strategy and ensure the successful...

Company Overview:Our client is a leading provider of sterile injectable pharmaceutical products, marketing and distributing a portfolio of sterile injectable drugs worldwide. They have a robust pipeline of products in development, including dosage forms in multidose vials, multiple presentations within the blow-fill-seal offering, and small molecule...

Social network you want to login/join with: Responsibilities Oversee the strategy implementation and operations for directing development of product registration submission, progress reports, supplements, amendments, or periodic experience reports.Interact with regulatory agency to expedite approval of pending registration.Serve as regulatory liaison...

Regulatory Affairs Coordinator sought by Asset Recruitment for a contract position at a pharmaceutical manufacturer in Carlow. The Regulatory Affairs Coordinator will provide critical support to ensure compliance with legal requirements related to EHS and industry best practices.The successful candidate will have EHS experience in the...

About the RoleWe are looking for an experienced R&D Engineer to support the product development of a cutting-edge device. The successful candidate will work closely with our cross-functional team to design, develop, and test the device, ensuring that it meets the required specifications and regulatory requirements.The ideal candidate will have a strong...

Job Description:Tn Ireland is looking for a skilled Global Regulatory Affairs Manager to join our team. The successful candidate will be responsible for interacting with regulatory agencies to expedite approval of pending registration and serving as regulatory liaison throughout the product lifecycle.Key Areas of Responsibility:Oversee the strategy...

TN Ireland is seeking a highly skilled Production Quality Specialist to join our team at Abbott.The ideal candidate will have a minimum NFQ Level 6 qualification in Engineering, Science, or Manufacturing and at least 2 years' experience in the food/medical/pharmaceutical industry.Responsibilities will include ensuring compliance with site and divisional...

Tn Ireland is a leading agri-food company dedicated to nourishing the world while protecting the environment.We are seeking an experienced regulatory affairs manager to join our team.Key Responsibilities:Ensure regulatory compliance across all Tn Ireland productsOversee regulatory updates and communicate changes to relevant teamsVerify supplier-provided...

**Product Development Opportunity**We are seeking a skilled R&D Engineer to contribute to the product development of a cutting-edge device. As an R&D Engineer, you will be responsible for designing sub-assemblies and finished devices, building and testing prototypes, and ensuring quality in the product's design.This is a great opportunity for someone who...

Job Description:We are seeking a skilled Global Regulatory Lead to join our team at Quanta Consultancy Services Ltd. As a key member of our organization, you will be responsible for ensuring compliance with regulatory requirements in the pharmaceutical industry.Key Responsibilities:• Act as a Responsible Person for Market Authorisation filings.• Manage...

Abbott is a leading manufacturer of life-changing technologies in diagnostics, medical devices, nutritional products, and branded generic medicines.Our manufacturing facilities are located in Clonmel, Cootehill, Donegal, Longford, Sligo, and Kilkenny, with a new facility opening in Kilkenny in 2024.We require a Quality Technician to join our team in...

About Cpl HealthcareWe are a leading healthcare recruitment agency providing temporary and permanent staffing solutions to the UK's National Health Service (NHS). Our goal is to connect talented professionals with rewarding career opportunities in the healthcare sector.Job Details:Job Title: Validation Engineer.Location: Longford.Type:...

In this Medical Devices Recruiter role, you will be responsible for delivering exceptional talent acquisition services to support Teleflex's EMEA business units. You will act as a brand ambassador, communicating proactively and timely on the status of searches, and providing consultative direction and industry expertise to hiring leaders. Your key...

Job Summary:We are seeking an experienced Product Registration Coordinator to join our regulatory affairs team. The successful candidate will be responsible for ensuring timely approval of new drugs, biologics or medical devices and continued approval of marketed products.Main Responsibilities:Serve as regulatory representative to marketing, research teams...

Required Skills and QualificationsBachelor's degree in Engineering or Science, preferably in Mechanical, Biomedical, or Chemical Engineering.7+ years' experience in medical device design or R&D with a successful track record of delivering products to market and supporting products after launch.Medical product design, research, and development...

At embecta, we are committed to empowering people with diabetes to live their best life through innovative solutions. As a Senior Product Engineer, you will play an integral part in the product lifecycle engineering team responsible for supporting various product lines in our $1 billion diabetes business.Job DescriptionThe Senior Product Engineer's primary...

Abbott is a global healthcare leader, providing life-changing technologies in diagnostics, medical devices, nutritional products, and branded generic medicines.The company has operations across ten sites in Ireland, employing around 6,000 people. Our manufacturing facilities are located in Clonmel, Cootehill, Donegal, Longford, Sligo, and Kilkenny.Kilkenny's...