A global medical technology firm is seeking a highly motivated Toxicology Specialist II in Galway, Ireland. The role involves supporting biocompatibility and toxicology processes for medical devices. Responsibilities include conducting evaluations and ensuring compliance with regulatory standards. An ideal candidate will have a BS/MS in Toxicology or a related field, along with 2-3 years of relevant experience and strong communication skills. This position offers an opportunity to work in a collaborative team environment. #J-18808-Ljbffr
A leading medical solutions company is seeking a Senior Electrical Test Engineer in Munster, Ireland, to support electronic medical device product transfers. The ideal candidate has an Hons BSc in electrical engineering and over 5 years of related experience. Responsibilities include failure analysis of electronic test equipment and collaborating with cross-functional teams to enhance product quality and efficiency. This is a permanent role with opportunities for career advancement and skill development. #J-18808-Ljbffr
Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we'll give you the opportunity to harness all that's within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we'll help you in advancing your skills and career. Here, you'll be supported in progressing - whatever your ambitions. Advancing possibilities for a brighter tomorrow Boston Scientific is seeking a highly motivated Toxicology Specialist II on a permanent basis to join our team. Job Purpose You will provide support for the global biocompatibility and toxicology processes and offers related biocompatibility and toxicology technical support to assigned business divisions in support of new product development, regulatory submissions and manufacturing and engineering changes to meet business objectives. Key Responsibilities Provides support for biocompatibility and toxicology processes initiated by department management and ensures the biocompatibility and toxicology related information and data are accurate, reliable, and support business objectives as consistent with Global Preclinical objectives and Quality Management System requirements. Demonstrates a primary commitment to patient safety and product quality. Under direction and mentorship of senior staff completes biocompatibility evaluations and chemical safety assessments as necessary to support divisional objectives. Provides input on the regulatory requirements related to medical device submissions, procedures, techniques, concepts and approaches used at divisional levels for biocompatibility and toxicology programs. Serves as a resource for biocompatibility and toxicology information for medical devices and pharmaceutical materials, which may include issues related to materials of animal origin, colorant additives, exposure assessments of chemicals, and other chemical toxicities as assigned. Communicates with internal customers on biocompatibility and toxicology issues and supports problem solving and resolution related to chemical risk assessments and biocompatibility assessments as assigned. Provides input on biocompatibility, chemistry and toxicology testing related to new investigational and strategic device development programs during new Technology and Product development programs. Participates in a Biocompatibility Training Program for all functional groups of device development teams based on standards and regulatory requirements. Education & Experience Academic Degree: BS, MS in Toxicology preferred or an alternative in chemistry, biochemistry, biology, biomedical science or a related field. 2-3+ years medical device knowledge with biocompatibility and toxicology experience preferable or an equivalent combination of education and experience. Professional with an understanding and application of principles, theories, and concepts in the biocompatibility of medical devices, ISO 10993 and toxicological risk assessor experience preferred; results and detail-oriented, and ability to multi-task while working against aggressive timelines. Comfortable in a dynamic environment and able to work independently as well as on teams. English level required: B2+ (80‑89%), excellent written and verbal communication skills. Experience of working with regulated authorities preferable. As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most — united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do — as a global business and as a global corporate citizen. So, choosing a career with Boston Scientific isn't just business, it's personal. And if you're a natural problem‑solver with the imagination, determination, and spirit to make a meaningful difference to people worldwide, we encourage you to apply and look forward to connecting with you! To search and apply for open positions, visit our careers page. At Boston Scientific, we recognise that nurturing a diverse and inclusive workplace helps us be more innovative. It is essential in advancing science for life and improving patient health. We stand for inclusion, equality, and opportunity for all. By embracing the richness of our unique backgrounds and perspectives, we create a better, more rewarding place for our employees to work and reflect the patients, customers, and communities we serve. Boston Scientific is proud to be an equal opportunity and affirmative action employer. Boston Scientific is committed to providing reasonable accommodations for applicants and employees with a disability. Should you require a reasonable accommodation during the recruitment process, please email To be considered for this role you will be redirected to and must complete the application process on our careers page. To start the process, click the Apply button below to Login/Register. #J-18808-Ljbffr
Additional Locations: N/A Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of diverse and high‑performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we’ll help you in advancing your skills and career. Here, you’ll be supported in progressing – whatever your ambitions. Advancing possibilities for a brighter tomorrow We are seeking a Senior Electrical Test Engineer on a permanent basis to join our team. Job Purpose: The candidate will be responsible for supporting the transfer of new electronic medical device products to the Clonmel Facility. Provide supervision, direction and mentoring of a technical team to validate and implement Test equipment and Manufacturing processes to production. Key Responsibilities: The ability to perform failure analysis on electronic test equipment. Using knowledge of standard system software applications, able to work with in‑house and external software developers to define and drive improvements and changes to test applications and systems to improve manufacturing test yields. Work with cross‑functional groups to improve product quality, lean efficiencies and test system efficiency’s and reduction in production fallout. Performs tests, writes reports and executes validations to medical device standard for Test and Manufacturing processes. Excellent data analysis and technical problem‑solving skills and project time management. Utilizing good documentation skills, complete regulatory submissions using change notice process and procedures. Work daily with quality, manufacturing, R&D and Design to efficiently implement product transfer. Work with PM to develop manufacturing project timelines. Education & Experience: Hons BSc degree in electrical engineering or related discipline. 5+ year’s relevant experience in a related industry. Experience in an electrical engineering-related environment essential. Strong working knowledge of process validations with proven problem‑solving abilities and the ability to project manage issues to closure. Knowledge of test software applications such as Lab View and C or C++. Experience in validations in the medical device industry and new product transfers would be an advantage. Requisition ID: 615765 As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most – united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do – as a global business and as a global corporate citizen. So, choosing a career with Boston Scientific isn’t just business, it’s personal. And if you’re a natural problem‑solver with the imagination, determination, and spirit to make a meaningful difference to people worldwide, we encourage you to apply and look forward to connecting with you! To search and apply for open positions, visit: https://bostonscientific.com At Boston Scientific, we recognise that nurturing a diverse and inclusive workplace helps us be more innovative. It is essential in advancing science for life and improving patient health. We stand for inclusion, equality, and opportunity for all. By embracing the richness of our unique backgrounds and perspectives, we create a better, more rewarding place for our employees to work and reflect the patients, customers, and communities we serve. Boston Scientific is proud to be an equal opportunity and affirmative action employer. Boston Scientific is committed to providing reasonable accommodations for applicants and employees with a disability. Should you require a reasonable accommodation during the recruitment process, please email To be considered for this role you will be redirected to and must complete the application process on our careers page. To start the process, click the Apply button below to Login/Register. #J-18808-Ljbffr
Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we'll give you the opportunity to harness all that's within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we'll help you in advancing your skills and career. Here, you'll be supported in progressing - whatever your ambitions. Advancing possibilities for a brighter tomorrow Boston Scientific is seeking a highly motivated Associate Manager (Equipment Engineer) on a permanent basis to join our team. Job Purpose: You will provide support for both new and current manufacturing equipment in regard to design, installation, troubleshooting, performance and validation activities. Key Responsibilities: Generate documentation for the detailed specification, design, development and testing of new equipment & automated systems Develop detailed knowledge & understanding in all aspects of automation systems including PLC, HMI, vision, robotics, PC software and databases. Develop a detailed understanding of Overall Equipment Effectiveness (OEE) and use of same to drive optimum equipment utilisation/operation. Identify equipment & automated system upgrades as part of continuous improvement programs, improving equipment/systems in terms of performance, qualify & availability. Provide technical support and make informed decisions on hardware and architecture selection Analyse, understand & fault-find as necessary on complex automation equipment Develop, test and install code changes to existing equipment under change control Maintain comprehensive documentation of code to medical device standards Actively participate among cross-functional teams to ensure projects are delivered on time and to required quality standards. Education & Experience: Degree in Automation/Electrical/Electronics/Mechatronics/Software or related Engineering discipline with at least 5 years relevant experience Experience working with automation systems & automated production equipment essential Excellent working knowledge of PLCs: Allen Bradley, Siemens, Beckhoff, GE Fanuc, Mitsubishi, Omron, Toshiba etc. Experience of HMI or SCADA programming and configuration Hands-on working experience with Allen Bradley and Siemens PLC's a distinct advantage. Hands-on working experience with Robotics & Vision system applications is an advantage Excellent analytical and Technical problem-solving skills essential Strong organisational skills Strong Leadership & Influencing skills Works well within a team environment and on own initiative Ability to document own work clearly and precisely Excellent communication skills As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most - united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do - as a global business and as a global corporate citizen. So, choosing a career with Boston Scientific isn't just business, it's personal. And if you're a natural problem-solver with the imagination, determination, and spirit to make a meaningful difference to people worldwide, we encourage you to apply and look forward to connecting with you! To search and apply for open positions, visit: At Boston Scientific, we recognise that nurturing a diverse and inclusive workplace helps us be more innovative. It is essential in advancing science for life and improving patient health. We stand for inclusion, equality, and opportunity for all. By embracing the richness of our unique backgrounds and perspectives, we create a better, more rewarding place for our employees to work and reflect the patients, customers, and communities we serve. Boston Scientific is proud to be an equal opportunity and affirmative action employer. Boston Scientific is committed to providing reasonable accommodations for applicants and employees with a disability. Should you require a reasonable accommodation during the recruitment process, please email To be considered for this role you will be redirected to and must complete the application process on our careers page. To start the process, click the Apply button below to Login/Register.
Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we'll give you the opportunity to harness all that's within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we'll help you in advancing your skills and career. Here, you'll be supported in progressing - whatever your ambitions. Advancing possibilities for a brighter tomorrow Boston Scientific is seeking a highly motivated Associate Packaging Engineering & Labelling Manager on a permanent basis to join our team. Job Purpose: The Associate Packaging Engineering & Labelling Manager supports Interventional Cardiology Therapies and Vascular Therapies (ICVT). This position works with cross-functional global teams to support many commercial product types across multiple divisions and manufacturing sites. In a Hybrid work mode, the Associate Packaging Engineering & Labelling Manager will manage and support a team of engineers and specialists. This team applies Packaging, Labelling & Graphics R&D principles and directives across projects including packaging design, design changes and enhancements, standards compliance, and cost-reduction improvement efforts. Key Responsibilities: Supervise 10+ direct reports (engineers/specialists and/or technicians) in Packaging, Labelling & Graphics R&D, including assignment and operational oversight of small to medium projects within the Sustaining organization. Technical and developmental strategy for direct reports. Develop direct reports by securing appropriate training, technical coaching, assigning progressively challenging tasks and conducting performance reviews. Monitor daily work operations and provide direction and guidance (technical and professional) to staff to achieve project goals. Lead and participate in Packaging, Labelling, & Graphics R&D initiatives. Influence the implementation of packaging changes/requirements to commercial devices. Supports the execution and documentation of Packaging, Labelling & Graphics R&D activities. Determines project staff assignments and schedules work to meet completion dates and project deliverables. Drives the development and continuous improvement of department tools and methodologies. Education & Experience: Required qualifications: Bachelor's degree in Packaging Engineering, or equivalent. Minimum of 5 - 7 years of Packaging R&D experience Minimum of 3 years medical device experience 2+ years of direct or indirect supervisory experience ISO 11607, relevant ASTM and ISTA standards, and Quality System understanding and demonstrated use Travel approximately
Additional Onsite Location(s): Cork & Clonmel Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we'll give you the opportunity to harness all that's within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we'll help you in advancing your skills and career. Here, you'll be supported in progressing - whatever your ambitions. Advancing possibilities for a brighter tomorrow We are seeking a Principal Talent Acquisition Specialist on a permanent basis to join our team. This role can be based at any of our three Ireland locations, Clonmel, Cork or Galway. At Boston Scientific, we value collaboration and synergy. This role follows a hybrid work model requiring employees to be on site at least three days per week. Job Purpose: The Principal Talent Acquisition (TA) Specialist will champion the TA strategy across the Ireland Region, working closely with Hiring Managers and HR Business Partners to understand the recruiting needs of the business; anticipate future talent demands, and proactively deliver sourcing solutions. You will lead and execute recruiting strategies in alignment with regional and global TA teams, supporting critical and emerging talent needs while reinforcing Boston Scientific's position as an employer of choice. This role requires confidence, collaboration and strategic influence to manage multiple stakeholders and competing priorities, while driving business success and a high-performing TA culture. Key Responsibilities: Coach and influence Hiring Managers and coordinate a diverse selection process to ensure optimal selection of candidates for available Senior and Executive Level positions. Develop and implement organizational recruiting strategies to attract the best qualified candidates. Work closely with the TA Ireland team to drive these strategies, with particular focus on niche and emerging roles in the region. Assign and allocate requisitions across the team with clarity, based on assessment of role type, areas of focus within the team and workload priorities. Act as a trusted mentor and advisor, fostering growth, confidence, and accountability within the TA team across the region. Drive purpose and accountability at daily stand up and team meetings, ensuring alignment, engagement and a culture of ownership. Prepare, extend, negotiate and finalise competitive job offers along with offering advice and coaching to members of the TA team to build confidence and knowledge in the job offer process. Communicate proactively and transparently with HR Business Partners and Hiring Managers, building trust through timely updates and confident engagement at all organizational levels. Own resolution of complex recruiting challenges, while mentoring the TA team to develop problem-solving skills and self-directed solutions. Support the already strong continuous improvement mindset within the team, suggesting and driving improvements within the current TA Hiring Process in the region and globally. Drive a technology-forward approach, advocating for innovative tools and AI solutions that elevate efficiency and candidate experience. Manage external partnerships, ensuring alignment with organizational standards and accountability for results. Act as a visible leader and contributor on specified Regional and Global initiatives Maintain full compliance with local laws and regulations, embedding best practices into all sourcing and hiring activities What we are looking for: Level 8 Honors degree in a relevant field A minimum of 7 years' experience working within a HR Function/Talent Acquisition environment, with at least 2 years in a leadership role Experience leading teams and supporting team development Proven ability to collaborate across regional and global functions Demonstrated ability to influence without authority, and build trusted relationships with stakeholders at all levels. Strong initiative, accountability, and resilience with a growth mindset and confidence in decision-making. Excellent relationship-building and stakeholder engagement skills. Demonstrated ability to lead with confidence and humility, inspiring trust and alignment beyond direct reporting lines. As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most - united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do - as a global business and as a global corporate citizen. So, choosing a career with Boston Scientific isn't just business, it's personal. And if you're a natural problem-solver with the imagination, determination, and spirit to make a meaningful difference to people worldwide, we encourage you to apply and look forward to connecting with you! To search and apply for open positions, visit: At Boston Scientific, we recognise that nurturing a diverse and inclusive workplace helps us be more innovative. It is essential in advancing science for life and improving patient health. We stand for inclusion, equality, and opportunity for all. By embracing the richness of our unique backgrounds and perspectives, we create a better, more rewarding place for our employees to work and reflect the patients, customers, and communities we serve. Boston Scientific is proud to be an equal opportunity and affirmative action employer. Boston Scientific is committed to providing reasonable accommodations for applicants and employees with a disability. Should you require a reasonable accommodation during the recruitment process, please email N/A To be considered for this role you will be redirected to and must complete the application process on our careers page. To start the process, click the Apply button below to Login/Register.
Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we'll give you the opportunity to harness all that's within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we'll help you in advancing your skills and career. Here, you'll be supported in progressing - whatever your ambitions. Advancing possibilities for a brighter tomorrow Boston Scientific is seeking a highly motivated Regulatory Affairs Specialist II on a permanent basis to join our team. Job Purpose: You will be responsible for Regulatory Affairs support of the product development process, submissions, maintenance of regulatory files and regulatory compliance primarily focused on pharmaceutical products and associated ancillary products (medical devices and components) for the administration of drug product. Key Responsibilities: Review and assess design and CMC changes, and prepare suitable submissions to ensure compliance to pharmaceutical regulatory requirements. Support and provide regulatory input for pharmaceutical quality system deliverables such as batch variation summaries, customer complaints, CAPA, deviations, NCMR, etc. for the manufacturing site(s). Prepare and submit OPDP, NDA and IND submissions and annual reports using eGateway via third party providers for USA submissions. Support clinical, sustaining projects and other product focused teams by giving direction on regulatory impact and requirements for proposed changes. Establish and maintain effective relationships and professional interactions with manufacturing sites CMC and Quality staff, third party suppliers, regulatory authority staff and reviewers. Support filings and maintenance of regulatory files globally. Management of local site licenses for manufacture and importation. Participate in regulatory authority inspections and audits. Monitor regulatory landscape and communicate changes or new requirements that may impact the product or quality system. Education & Experience: Degree in Life sciences (e.g., Chemistry, Biology, etc.). Minimum requirement of pharma industry experience 1-3years, ideally in a regulatory capicity. Medical device regulatory experience desirable. Demonstrated leadership and organizational skills. Understanding of commercial business. Demonstrated ability to handle multiple projects. Working knowledge of local regulations and guidelines related to drug development and registration. Excellent verbal and written communication skills. Work successfully within a team environment and as an individual contributor. Flexible and ability to adapt to changing regulatory environment and business needs. Proficient use of technology including MS office programs and Internet resources. As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most - united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do - as a global business and as a global corporate citizen. So, choosing a career with Boston Scientific isn't just business, it's personal. And if you're a natural problem-solver with the imagination, determination, and spirit to make a meaningful difference to people worldwide, we encourage you to apply and look forward to connecting with you! To search and apply for open positions, visit: At Boston Scientific, we recognise that nurturing a diverse and inclusive workplace helps us be more innovative. It is essential in advancing science for life and improving patient health. We stand for inclusion, equality, and opportunity for all. By embracing the richness of our unique backgrounds and perspectives, we create a better, more rewarding place for our employees to work and reflect the patients, customers, and communities we serve. Boston Scientific is proud to be an equal opportunity and affirmative action employer. Boston Scientific is committed to providing reasonable accommodations for applicants and employees with a disability. Should you require a reasonable accommodation during the recruitment process, please email To be considered for this role you will be redirected to and must complete the application process on our careers page. To start the process, click the Apply button below to Login/Register.
A leading medical device company is seeking a Senior Validation Engineer in Galway. The role involves leading and managing validation activities while ensuring compliance with global standards and best practices. Ideal candidates will have at least 6 years of experience in Validation Engineering and possess a strong background in project management and team leadership. This position offers opportunities for professional growth and contributions towards innovative medical solutions. #J-18808-Ljbffr
Overview Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we will give you the opportunity to harness all that's within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we’ll help you in advancing your skills and career. Here, you’ll be supported in progressing - whatever your ambitions. Advancing possibilities for a brighter tomorrow Job Purpose Seeking a Senior Validation Engineer within the Global Equipment Engineering function to lead and manage day to day Validation activities across Galway and other sites as required. This role combines strong leadership and project management skills along with technical expertise in equipment and software validation. The ideal candidate will possess excellent analytical, system analysis and problem-solving skills, excel at guiding teams, driving complex projects to completion and thrives in a fast paced, collaborative team environment. Core Leadership & Project Management Responsibilities Manage and mentor a team of validation engineers (staff & contractor), providing guidance, training, and career development support. Motivate and inspire individuals to achieve results while building a high-performing, engaged team culture. Provide project management, validation oversight and direction through all phases of the project lifecycle. Ensure validation deliverables meet project timelines, budgets, and scope, addressing changes proactively. Ability to assess schedule deviations and assist in the development of alternative methods for corrective action at the project level. Develop and enhance cross-functional team relationships and work collaboratively to identify and resolve issues. Key Technical Responsibilities Ensure equipment and software validations comply with global and site standards, and applicable regulatory requirements, while maintaining up-to-date validation procedures. Ensure best validation practices are employed by the Equipment Engineering Group to maximise effectiveness and minimise non-value-add work. Works closely with customers to understand requirements and propose creative, cost-effective validation solutions. Partner with global engineering teams to share best practises and align validation strategies. Travels to various BSC sites to coordinate and oversee validation activities across multiple BSC sites as needed. Champions continuous improvement initiatives in validation processes, leveraging data-driven insights to enhance efficiencies. Education & Experience Level 8 Bachelor's Degree (240 credits) in a relevant engineering discipline with a minimum of 6+ years' experience in a medical device industry. 6+ years' experience in Validation Engineering, including protocol development & execution. Experience leading and developing teams, acting as a role model, and giving clear guidance and support. Demonstrated ability to manage groups with different skill levels effectively. Advanced knowledge of software validation Lifecycle Qualification & Risk based qualification strategies. Proven ability to qualify and validate highly complex PC and PLC based automated systems. Experience with Databases & multi-technology platform integrations is an advantage. Strong project management/project lead experience with excellent interpersonal skills, PMP qualification is a distinct advantage. Company Commitment As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most – united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do – as a global business and as a global corporate citizen. We encourage you to apply and look forward to connecting with you! To search and apply for open positions, visit our careers page. Boston Scientific is proud to be an equal opportunity and affirmative action employer. Boston Scientific is committed to providing reasonable accommodations for applicants and employees with a disability. Should you require a reasonable accommodation during the recruitment process, please email. #J-18808-Ljbffr
