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- ...Month Contract Join a high-impact project at the forefront of medical device innovation. Support the design and development of a cutting-... ...& development Strong understanding of design controls and regulatory standards (FDA, ISO, IEC) Excellent documentation and process...RegulatoryMedical deviceContract workLong term contract
- ...protocols, reports & amendments of the Quality Management System ensuring compliance with the latest Regulatory Agencies (HPRA, FDA) directives / requirements within the Medical Device and Pharma Sector. Generate applicable quality documentation in conjunction with validation...RegulatoryMedical device
- ...Your New Job Our client is a specialist Pharmaceutical Manufacturing firm that have a... ...compliance with all safety, quality, and regulatory programs and initiatives across daily... ...essential. Previous experience in a medical device or regulated manufacturing environment...RegulatoryMedical devicePermanent employmentNight shiftRotating shift
- ...procedures. The Senior Quality Engineering Specialist will manage the quality aspects of West... ...compliance with relevant regulations; regulatory requirements; international standards;... ...environment, ideally in the Medical Device / Pharmaceutical sectors. ~ Desirable...RegulatoryMedical deviceLocal area
- ...to receive an alert: Title: Senior Specialist, Quality, Integrated Systems Requisition... ...multiple concurrent projects to ensure regulatory and quality compliance is maintained... ...experience in a regulated industry (e.g., Medical Device), including Product Manufacturing and...RegulatoryMedical device
- ...Join a leading medical device and pharmaceutical company in Waterford, where innovation, compliance, and quality are at the heart of everything... ..., reports, and amendments in line with HPRA, FDA, and other regulatory requirements. Prepare and maintain quality documentation...RegulatoryMedical deviceFull timeImmediate start
- ...800 work together at a state-of-the-art biopharmaceutical and medical device campus. Recognised through multiple local and national awards,... ...activities. Authors and reviews process development sections of regulatory and technical documents, study reports and technology transfer...RegulatoryMedical deviceFixed term contractLocal areaFlexible hours
- ...~ Extensive hands-on experience of preventive / reactive maintenance and technician supervision / interaction. ~ Knowledge of medical device and/or pharmaceutical production preferred (cGMP / FDA regulated environment). ~ Self-directed with excellent communication skills...Medical deviceShift work
- ...~3-6 years’ experience in a manufacturing environment (high volume automated assembly experience would be an advantage as would medical device manufacturing experience). ~ Travel as necessary to support equipment buy-offs and training at vendor / customer sites. For...Medical deviceFor contractors
- ...Qualified trades personnel with industrial experience are also considered. Automation/robotics experience (high volume). Medical device manufacturing experience (desirable). Experience with pneumatics, electronics, hydraulics, PLCs, servo motors, vision systems,...Medical deviceShift workSundayMonday to Wednesday
- ...initiatives to implementation and management. Conducting regular audits, assessments and inspections and ensure sites are adhering to regulatory compliance Coaching and supporting project teams to generate new solutions to common, everyday issues. Working closely with...RegulatoryPermanent employmentFor subcontractorLocal areaFlexible hours
- ...’s degree (Honors) in Engineering (Level 8). Minimum of 2 years of experience in manufacturing engineering , preferably in medical device or pharmaceutical industries. Proficiency in MS Office and CAD software such as SolidWorks (or equivalent). Experience...Medical deviceFull timeImmediate startDay shiftMonday to Thursday
- ...central to ensuring we deliver a reliable, high-quality consumer device that seamlessly integrates with our software and user experience... ...electronics or fluidics-based systems (e.g., beverage machines, medical devices, or lab instrumentation). Strong proficiency in 3D CAD...Medical deviceFull timeHybrid work
- ...Experience ~ Graduate or individual with 1+ years experience in a similar role (Micro/Particulate testing) within the pharmaceutical / medical devices / manufacturing industry. Preferred Knowledge, Skills and Abilities Good knowledge and understanding of principles of...Medical deviceLocal area
- ...discipline. Graduate or individual with 1 - 3 years experience in a similar role (Chemistry / QC testing) within the pharmaceutical / medical devices / manufacturing industry. Preferred Knowledge, Skills and Abilities Good knowledge and understanding of principles of...Medical deviceLocal areaShift work
- ...technical discipline. Work Experience ~5+ years’ experience in Energy Engineering for the pharmaceutical, biopharmaceutical or medical device industry. ~ Good working knowledge of MS office applications, including Word, Excel, PowerPoint, Outlook etc. ~ Knowledge and...Medical deviceLocal area
- ...diversify to serve patients around the world. Today, a team of almost 800 works together at a state-of-the-art biopharmaceutical and medical device campus. Recognized through multiple local and national awards, Sanofi Waterford offers flexible working and access to a world of...Medical deviceFixed term contractLocal areaFlexible hoursShift work
- ...maintenance staff. Excellent problem-solving abilities and the capacity to make sound decisions under pressure. Solid understanding of regulatory requirements and standards related to building services and facilities maintenance. Exceptional communication and interpersonal...RegulatoryContract work
- ...financial operations and reporting Manage budgeting, forecasting, and financial planning Ensure compliance with all relevant regulatory and tax requirements Liaise with auditors and external stakeholders Provide strategic financial guidance to the management team...RegulatoryLong term contract
- ...by working closely with the marketing and sales teams. Drive the development of new innovations while ensuring market needs and regulatory requirements are met. Develop and maintain a technology roadmap for advancing core technologies to maintain a competitive and sustainable...Regulatory
- ...that may arise during construction Ensure that all relevant permits and licenses are obtained and that all projects comply with regulatory requirements Preferred Candidate Experience: Bachelor's degree in Civil Engineering or related field Professional Engineering...RegulatoryContract workFor contractorsFor subcontractor
- ...Coordinate with logistics, supply chain, and other departments to ensure timely delivery of materials and services. Ensure quality/ regulatory compliance procedures are implemented and followed by site personnel Manage scheduling, resource allocation, and conflict...Regulatory
- ...Maintenance Supervisor- Waterford A multinational Medical device Manufacturer is currently seeking a skilled Maintenance Supervisor to join its team. As a Maintenance Supervisor, you’ll oversee a talented team and ensure optimal performance of equipment while maintaining...Medical devicePermanent employmentShift work
- ...financial statements in line with applicable accounting principles and audit standards. Ensure Compliance : Stay up to date with regulatory changes and ensure all audits comply with the latest laws and standards. Risk Assessment : Identify audit risks and take...Regulatory
- ...effective development and fostering of a strong team working culture. # Promote a quality culture and ensure compliance with all regulatory requirements including FDA and cGMP. # Conduct and manage performance appraisals for operators and identify and implement appropriate...RegulatoryShift workWeekend work
- ...Safety & Health and welfare Thorough knowledge of current environmental, health and safety legislation Experience in dealing with Regulatory Bodies Internal Auditing Experience would be beneficial Experience with ISO 45001 Standards. Skills and competencies: Be...RegulatoryFor contractorsFor subcontractorRotating shift
- ...years of experience in construction management in Ireland. In-depth knowledge of construction contracts, procurement processes, and regulatory requirements. Strong budgeting, financial management, and risk assessment skills. Excellent organizational and problem-solving...RegulatoryContract workFor subcontractor
- ...compliance to GMP certification by conducting and reporting internal reviews. Co-ordinates, prepares and is the lead for all internal, regulatory, supplier and customer audits. Operational Activities: Administration of quality documents, continuous improvement initiatives...RegulatoryContract work
- ...qualified trades personnel. Experience in high-volume automation/robotics is required. Prior experience in a healthcare or medical device manufacturing environment is highly desirable. Knowledge of Pneumatics, Electronics, Hydraulics, Programmable Controllers, Servo...Medical deviceFull timeImmediate start
- ...THE APPLICATION FORM FULLY, CV'S ARE NOT ACCEPTED********* Principal Duties and Responsibilities Professional / Clinical The Medical Scientist,Senior (Histology) will : Be required to support the principle that the care of the patient comes first at all times and...Permanent employmentFull timeWork at officeLocal area