Get new jobs by email
- ...As a Staff Regulatory Affairs Specialist based in Cork, you will play a key role in ensuring regulatory compliance for Stryker’s medical devices across global markets. In addition, you will support product transfers between Stryker manufacturing sites and international markets...RegulatoryMedical deviceWork from homeHome officeFlexible hours2 days week
- ...equipment based on analysis of specifications, reliability, and regulatory requirements. Work with quality engineers to develop component... ...Experience in post-additive manufacturing or medical device manufacturing. Knowledge of MES systems, Industry 4.0 technologies...RegulatoryMedical deviceContract workLocal area
- ...automated, innovative, cost effective and meet all Quality and EHS regulatory requirements • Manages and executes production equipment... .... • Working knowledge of the following preferrable: -Medical Device experience -Working knowledge of Validation processes (IQ/OQ...RegulatoryMedical device
- ...under minimal supervision, work with R&D, Quality, Manufacturing, Regulatory, Clinical, Marketing, and Project Management to ensure project... ..., developing, modifying, and verifying components/modules for medical devices. The candidate should quickly process and assimilate...RegulatoryMedical deviceWorldwide
- ...Engineer (R&D) to spearhead the development of a ground-breaking medical device aimed at tackling blood loss during medical procedures. This... ..., design requirements and test strategies which apply to regulatory requirements • Independently create or refine engineering documentation...RegulatoryMedical devicePermanent employmentHybrid work
- ...and operational procedures and practices comply with current regulatory requirements and corporate standards. Adopt new products to... ...degree in chemistry or pharmacy with experience in Pharma or medical device Minimum 2 years experience in people management. Must have...RegulatoryMedical deviceWorldwideFlexible hours
- ...This position provides experience working in a regulated medical device company. You will have the opportunity to develop and apply basic knowledge of quality, regulatory, and legal frameworks, requirements, legislation, processes, and procedures. Additionally, this opportunity...RegulatoryMedical deviceFlexible hours
- ...Position : LOTO (Lockout/Tagout) Engineer Industry : Medical Devices / Safety Engineering / Compliance Location : Ireland (On-site... ...central to safeguarding staff, patients, equipment integrity, and regulatory compliance. Key Responsibilities Identify and document...RegulatoryMedical devicePermanent employmentFull timeLocal area
- ...leading the verifying activities for compliance to the European Medical Device Regulations (MDR) for Stryker products, developing and... ...knowledge and understanding of RA frameworks, ensuring fulfilment of regulatory obligations and timely market access in EU countries. What...RegulatoryMedical devicePermanent employmentLocal areaHybrid work
- ...Bishopstown, Cork, and has developed a breakthrough single-use medical device, Solo+ TTD, which addresses pain points of the current... ...procedures, work instructions, and quality standards to ensure regulatory compliance. Provide technical support and troubleshooting expertise...RegulatoryMedical device
- ...Job Title : Senior Regulatory Affairs Location : Bishopstown, Cork Benefits: Competitive Salary, Bonus, Pension, Healthcare +... ...recently been acquired and have developed a breakthrough single-use medical device, that addresses pain points of the current treatment of the...RegulatoryMedical deviceContract work
- ...economic trends; stakeholder concerns; and regulatory issues; and determine implications for... ...for products addressing serious or unmet medical needs. Negotiate with regulatory authorities... .... Technical knowledge of medical device product lines. Excellent communication...RegulatoryMedical device
- ...provide quality assurance and quality control to ensure we meet regulatory standards, and procure the needed goods and services to... ...operating environment such as the biologics, pharmaceutical or medical device sectors is desirable though not essential. Previous packaging...RegulatoryMedical deviceTemporary workWorldwideShift work
- ...Development Executive to develop and execute a sales strategy for medical device testing, consultancy, and packaging services. This role will... ...technical understanding of laboratory testing services, regulatory requirements, and industry trends. Responsibilities Include...RegulatoryMedical deviceContract workWork from home
- ...Associate Director of Quality to become part of a top-tier medical device organization headquartered in Cork . This globally recognized... ...is responsible for delivering expert guidance on quality and regulatory compliance to ensure that all pharmaceutical products produced...RegulatoryMedical devicePermanent employmentLocal area
- ...and will play a critical role in maintaining the quality and regulatory compliance of our biopharmaceutical products. You will work closely... ...quality assurance within a biotechnology, pharmaceutical, or medical device manufacturing environment. ~ Strong knowledge of cGMP, FDA,...RegulatoryMedical deviceLocal area
- ...Responsibility Maintain EHS management system in line with internal and regulatory requirements, ensuring procedures and documents are up to date... ...or equivalent. Proven success as an EHS Manager in a large Medical Device or related manufacturing facility is desirable. Ongoing...RegulatoryMedical device
- ..., ensuring robust process risk management and compliance with regulatory standards. The ideal candidate will drive cross-functional collaboration... ...years of experience in a regulated manufacturing environment (Medical Device, Pharmaceutical, Biomedical, or Automotive). ~ Minimum of 3+...RegulatoryMedical deviceHybrid work
- ...Maintenance of EHS management system in line with internal and regulatory requirements ensuring procedures and other documents are kept... ...A proven track record of success as an EHS Manager in a large Medical Device (or related industry) manufacturing facility is desirable. ~...RegulatoryMedical deviceLocal area
- ...and the global leader in Foot & Ankle solutions. Our innovative medical devices help transform lives every day. We are seeking a Staff... ...experts across Quality, Biomechanical Testing, Manufacturing, Regulatory, Clinical, Marketing, and Project Management to shape the future...RegulatoryMedical deviceWorldwide
- ...safe, high-quality clean and sterile products while maintaining regulatory compliance Oversight of Micro & Sterility key processes... ...Thorough knowledge and understanding of US and International Medical Device Regulations and standards in area of expertise (Microbiology)...RegulatoryMedical deviceLocal areaHybrid work
- ...development and launch. The role involves working within the medical device quality management system, managing a cross-functional team, and... ...updates to stakeholders. Aligning project strategies with regulatory pathways and requirements. Supporting supply chain strategies...RegulatoryMedical devicePermanent employmentHybrid work
- ...to work at the intersection of advanced medical technology and work on patient impacting... ...and verify components/modules for medical devices • Translate design inputs to engineering... ...requirements and test strategies which apply to regulatory requirements • Independently create or...RegulatoryMedical devicePermanent employmentHybrid work
- ...lead a high-performing team at the forefront of innovation in medical device manufacturing. In this hands-on leadership role, you’ll play... ...transfer meets the highest standards of quality, safety, and regulatory compliance. Your work will directly shape the future of life-changing...RegulatoryMedical device
- ...cv to ****@*****.*** Role: Regulatory Associate Location: Bishopstown, Cork... ..., in‑office ear‑tube insertion device. They've scaled from Irish clinical success... ...regulations. You must have a working knowledge of medical device regulatory requirements and...RegulatoryMedical deviceContract workLong term contractWork at officeImmediate startWorldwideHybrid workFlexible hours
- ...A dynamic and fast-paced medical device start-up based in Galway, is seeking a Quality Engineer I to join their growing team. Location... ...needed. Support updates and gap assessments for applicable regulatory standards and guidance. Participate in supplier quality management...RegulatoryMedical deviceContract workVisa sponsorshipLocal areaImmediate startWork visa
- ...excellence, delivering high-quality orthopaedic devices that improve the lives of millions of... ...~ Oversee engineering compliance with regulatory standards (e.g., FDA, ISO 13485) and internal... ...role. ~ Strong background in the medical device or orthopaedic manufacturing sector...RegulatoryMedical deviceLong term contractWorldwide
- ...to product development teams, preclinical team, quality, and regulatory teams. Quick learning and a desire to understand requirements... ...worked in a global team setup ~3–6 years of experience in a medical device or other regulated environment Preferred Qualifications...RegulatoryMedical device
- ...budget, and to performance requirements. Working within the medical device quality management system, this leader manages a cross-... ...project status at various business forums. # Coordinate with Regulatory Affairs to ensure project strategies meet regulatory requirements...RegulatoryMedical devicePermanent employmentTemporary workHybrid work
- ...delivery, budget adherence, and performance standards. Within the medical device quality management system, this leader manages a cross-... ...on project status across business forums. # Coordinate with Regulatory Affairs to align project strategy with regulatory requirements...RegulatoryMedical devicePermanent employmentTemporary workHybrid work