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 Manufacturing Engineering Manager on a permanent basis to join our team. Job Purpose: Provides daily support in the PCT mouldings area for products, processes, materials, and equipment in order to achieve production unit goals (i.e., People & Safety, Quality, Service, NPE, Cost & Productivity). Key Responsibilities: Lead a team of operations engineers and technicians in improving our processes across People, Quality, Service and Cost. Liaise with management within the Production Unit in developing strategic goals and planning effectively. Provide direction on product and process issues, while ensuring effective communication to key stakeholders. Support the introduction of new products and processes, while managing close relationships with other departments both internally and externally within the corporation. Demonstrate a primary commitment to patient safety and product quality. Develops engineers and technicians on technical and leadership competencies aligned to our culture. Use our processes and systems to run the business, drive improvement and ensure compliance to requirements. Maintain a valid capacity model and conduct adequate advance planning for required capital funding aligned with production requirements. Evaluates in conjunction with EHS new equipment/processes/chemicals for environmental impact/effect to eliminate or lessen such impacts/effects Sponsor problem solving/process improvement projects. Education & Experience: Honours Bachelor's Engineering Degree (Level 8 - 240 credits). Polymer qualification a distinct advantage. Experience in injection moulding ME line support of 5 years minimum. This experience in a Medical Device / strongly regulated environment a distinct advantage Demonstrated experience leading and supporting teams to achieve organisational goals Expert in problem solving. A strategic team-player, with deep-rooted initiative and accountability. Good technical capabilities, communication skills, teamwork abilities and initiative. 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 We are seeking a Clinical Software Engineer III (Audit Support) on a permanent basis to join our team. This role can be based at any of the three Irish Sites or at our Costa Rica Site Job Purpose: The Clinical Software Engineer P3 (Audit Support) role provides experienced, hands-on operational support for clinical and pre-clinical software audit and vendor cybersecurity activities across Clinical, PreClinical, and IT environments. This role serves as a critical connector between Clinical and PreClinical teams, IT Security, Quality, and vendor owners, requiring a strong understanding of regulated documentation practices and systems. By owning day-to-day audit operations, documentation coordination, and tooling optimization, this position enables the broader audit team to focus on strategy, process maturity, and continuous vendor improvement while maintaining a patient-first focus on quality, compliance, and data integrity. Key Responsibilities: Provide operational audit support spanning both Clinical and PreClinical organizations, ensuring alignment of cybersecurity and vendor risk activities across development and lifecycle stages. Act as a primary liaison between IT Security, Boston Scientific business owners, Clinical and PreClinical stakeholders, and external software vendors. Analyze audit and risk data to identify gaps, trends, and opportunities for vendor and process improvements that inform risk-based decision making. Own execution of routine and moderately complex audit support activities, including vendor evidence collection, review coordination, issue tracking, and follow-up. Maintain and optimize vendor risk, audit, and remediation records within the ServiceNow platform, ensuring data accuracy, completeness, and audit readiness. Coordinate controlled documentation associated with audits and vendor assessments, including proper storage, versioning, and traceability within document management systems such as Windchill. Apply knowledge of documentation governance, retention, and controlled workflows to ensure compliance with quality and regulatory expectations. Design, build, and maintain dashboards and reporting that provide visibility into vendor cybersecurity posture, audit status, trends, and key risk indicators across Clinical, PreClinical, and IT vendors. Support standardization and continuous improvement of audit support processes, templates, and workflows. Ensure timely, clear communication of audit requirements, findings, and remediation actions to internal stakeholders and vendors. Independently manages operational audit support for a defined portfolio of Clinical and PreClinical software vendors. Enables consistent execution of audit and cybersecurity activities across organizational boundaries and development phases. Reduces low-level operational workload for senior audit staff, allowing greater focus on strategy, risk prioritization, and vendor improvement initiatives. Improves documentation quality, traceability, and audit readiness through effective use and optimization of controlled document management systems. Provides a strong foundation for growth into senior audit, cybersecurity risk, vendor management, or program leadership roles. Education & Experience: Level 8 Honors Bachelor's degree in Engineering, Information Systems, Computer Science, or a related technical discipline. 5+ years of relevant experience in cybersecurity, IT compliance, audit support, or vendor risk management within regulated environments. Hands-on experience with ServiceNow (IRM, TPRM, or related modules). Working knowledge of document control and documentation management systems such as Windchill. Demonstrated ability to provide operational support across cross-functional and cross-lifecycle teams. Strong organisational skills and ability to manage multiple workstreams and stakeholders. Experience supporting clinical, preclinical, or medical device software environments desirable. Familiarity with cybersecurity and risk frameworks (NIST, ISO 27001, SOC) desirable. Experience working with third-party vendors and outsourced service providers desirable. Experience operating within Quality Management Systems (QMS) desirable. Exposure to continuous improvement or Lean methodologies desirable. 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 We are seeking a Maintenance Technician S2 on permanent basis to join our team. Job Purpose: Reporting to the Senior Maintenance Engineer, the role of Maintenance Technician is to provide electrical and mechanical maintenance support to ensuring that equipment asset performance is maximised. A high maintenance standard is a must as is adherence to quality standards and safety. Key Responsibilities: Maintain Planned Preventative Maintenance through CMMS System (BMRAM) Carry out the maintenance of production process equipment, to include planned preventative and unplanned maintenance tasks. Carry out detailed root cause analysis on breakdowns to implement corrective repairs. Review planned preventative maintenance procedures (PM's) to improve their quality and effectiveness and manage amendments to same though the Senior Maintenance Engineer and/or CMMS admin where appropriate. Provide support to the Line support team and systems to maximise equipment uptime for the Value Streams in accordance with the requirements of the business. Assist the department in achievement of world class equipment uptime (M.T.T.R. and M.T.B.F. metrics) through the utilisation of downtime and OEE (Overall Equipment effectiveness) data. Work with Senior Maintenance Engineer and Value Streams to identify & implement projects for permanent solutions of known recurring equipment downtime issues. Promote an environment of continuous improvement and innovation in line with lean thinking and Operational Equipment Excellence. Participate and support the 5s + Safety program within the Value Streams & Equipment Management areas as appropriate. Promote and participate in the Maintenance departments Continuous Improvement Program. Reporting of work status on a timely basis to the Senior Maintenance Engineer and Value Stream team leaders as appropriate. Maintain log of activities carried out on equipment i.e. actual hours works, spare parts used, equipment downtime etc using the site Computerised Maintenance Management System (BMRAM). Ensure compliance to all aspects of the Company's Health, Safety and Environmental procedures. Ensure all activities are carried out in accordance with the GMP requirements. Education & Experience: NFQ Level 6 Higher certificate qualification in STEM, Automation Systems or or Mechatronics Relevant working knowledge of an FDA regulated industry and GMP requirements. Experience working in a Cleanroom environment Previous experience working with a CMMS (preferably BMRAM) in a maintenance role Minimum 3-5 years' experience in a regulated manufacturing environment. Knowledge & Experience in OEE systems/software applications Strong electrical and electronic repair and diagnostic skills Strong mechanical systems problem solving & repair skills Experience in pneumatic fault finding and repair Experience with high-speed automated manufacturing equipment Experience with maintenance of Vision inspection systems Experience in the operation & programming of Programmable Logic Controllers, Drives, HMI's etc. Demonstrate levels of theoretical knowledge with practical application. Good teamworking & communication skills. Good computer skills. Experience in another simiolr technician position is advantageous. 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 Senior Regulatory Affairs Specialist on a permanent basis to join our team. Job Purpose: The Senior Regulatory Affairs Specialist - eRIM Process Support supports the expansion of features in Boston Scientific's electronic Regulatory Information Management (eRIM) system and the adaptation of processes to integrate the technology. This individual works under direction of the eRIM Process Lead (Req 624200) on the business support team and partners closely with the Product Owner, Data Lead, Change Management and Training Lead, and cross-functional Regulatory Affairs stakeholders to ensure global regulatory processes are clearly defined, fit for purpose and scalable across phases of the eRIM program. This role will report into Global Regulatory Affairs Operations, a corporate/global function. As part of our continued team growth, we are expanding our team within this function. Please visit the Boston Scientific Careers site to explore related openings and apply to the position that best matches your background. At Boston Scientific, we value collaboration and synergy. This role follows a hybrid work model requiring employees to be in our local office at least three days per week. Key Responsibilities: Process development and ownership Serve as a core team member for the eRIM program, contributing to the design and implementation of the global RIM solution and operating model. Support the transformation, development, and documentation of end-to-end regulatory business processes aligned with eRIM program phases, including worldwide authorizations and registrations, regulatory submission planning and tracking, submission and correspondence storage, international change notification and response and future-state regulatory processes beyond initial go-live. Define clear process flows, business rules and decision points that align with regulatory requirements and system capabilities. System and requirements collaboration Partner with the Product Owner to translate regulatory process needs into clear system requirements, user stories and acceptance criteria. Collaborate with the Data Lead to define regulatory data elements and attributes, support data standards and governance decisions and ensure alignment between processes, data capture and downstream use. Act as a key business liaison to ensure regulatory processes are accurately reflected in system configuration. Documentation and work instructions Author and maintain high-quality process documentation, including work instructions (WIs), standard operating procedures (SOPs), knowledge sharing documents (KSDs) and other supporting guidance and training-ready materials in collaboration with the Change Management and Training Lead. Ensure documentation is clear, concise and suitable for a global regulatory audience and external auditing bodies. Stakeholder engagement and communication Engage global and regional Regulatory Affairs stakeholders to gather input, understand current-state practices and assess the impact of new processes. Evaluate diverse feedback, incorporate value-added input and clearly communicate decisions and rationale. Clearly articulate process expectations, roles and responsibilities across functions and regions. Change enablement and adoption Support change management activities by providing strong process context and rationale for change. Partner with training and change leads to support effective rollout, adoption and continuous improvement of eRIM processes. Serve as champion for the strategic advantages of an enterprise-wide RIM system. Education & Experience: Honours Bachelor's degree (level 8) in life sciences, engineering, pharmacy, public health, communications or a related discipline. Minimum of 5 years' experience in Regulatory Affairs or related compliance experience within the medical device industry. Demonstrated working knowledge of FDA, EU or international regulatory frameworks impacting medical device authorization and maintenance. Proficiency with Microsoft Office applications, including Word, Excel and PowerPoint. Preferred qualifications: Strong written and verbal communication skills, including the ability to translate complex regulatory requirements into clear, actionable guidance, with demonstrated writing, editing, critical-thinking skills and attention to detail. Experience with electronic Regulatory Information Management (eRIM) systems, such as Rimsys, Veeva or Honeywell. Familiarity with Boston Scientific Regulatory Affairs processes and organizational context. Demonstrated ability to influence without authority and collaborate effectively within cross-functional teams. Experience supporting large-scale system or process transformation programs. Experience working in global regulatory environments with regional and country-specific requirements. Strong organizational skills with an audit-ready mindset and documentation discipline. Learning agility and a continuous improvement orientation. Pragmatic problem-solving skills with a coaching mindset. 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. Job Purpose: The Quality Engineer will serve as a key Quality representative within the Galway Magellan Go Live readiness Program. You will ensure Magellan solutions meet Quality System requirements, Galway requirements, support testing and deployment activities, and drive quality-focused process improvements. A critical requirement for this position is the ability to understand existing SAP functionality in ECC and work towards understanding the new functionality in S4 to become a super user. This role offers the opportunity to work on a project for a site SAP rollout involving planning, stakeholder engagement and execution with cross functional site and global Magellan personnel. Key Responsibilities: Demonstrate strong commitment to the Quality Policy and compliance with 21 CFR Part 820, ISO 13485, and BSC Quality System requirements. Build quality into all aspects of work and support compliant solution design, site activities for readiness. Conduct business, quality and process impact assessments and execute readiness in conjunction with site cross functional teams and Magellan business support Apply effective problem-solving methodologies to resolve quality issues. Business Readiness Support for site Magellan implementation Understand quality-related business requirements and translate info to Magellan functional reps to ensure requirements are understood. Work with business areas through the duration of site readiness ensuring business requirements are understood, Magellan solution is appropriate and business readiness (training, business, quality and process changes) is appropriate Partner with Magellan business quality reps to ensure quality requirements are understood and implemented. Facilitate workshops to evaluate current-state and future-state workflows if required Recommend quality process improvements and system enhancements. Solution Delivery & Testing Work in conjunction with Business Magellan team to develop test plans, complete test execution and work through testing results with Magellan teams for new S4 functionality. Work in conjunction with Business Magellan team to Develop test plans for business readiness for SAP functionality already implemented under previous implementations. Stakeholder Collaboration & Communication Act as liaison between Galway site business teams, Galway site Magellan teams and global quality Magellan teams. Communicate program/site risks, issues, and decisions clearly to Galway team and leadership if required . Provide coaching and SME support to business Quality Engineers and Technicians. Support CAPA, Lean, and continuous improvement initiatives. Audit & Quality Systems Support Support audit readiness and document non-conformances if applicable. Recommend appropriate corrective and preventive actions. Contribute to development of streamlined quality business systems. Education & Experience: Hons bachelor's degree in Engineering, Science, or related field. 3+ years of Quality Engineering or Quality Systems experience in a regulated environment. Strong SAP ECC knowledge will be extremely valuable for this role as it will help to be able to translate from ECC to S4 Strong understanding of ISO 13485 and 21 CFR 820. Experience supporting process or system transformation initiatives. Excellent communication, documentation, and stakeholder management skills. Preferred Qualifications Systems and process thinker with strong analytical skills. Comfortable operating in ambiguity with ability to bring clarity. Strong relationship builder and collaborator. High accountability, professionalism, and attention to detail. Able to work effectively across functions and with global teams. Strong analytical and technical writing skills. This is hybrid role - Min 3 days per week onsite Requisition ID: 624897 Boston Scientific transforms lives through innovative medical technologies that improve the health of patients around the world. As a global medical technology leader for more than 45 years, we advance science for life by providing a broad range of high-performance solutions that address unmet patient needs and reduce the cost of healthcare. Our portfolio of devices and therapies helps physicians diagnose and treat complex cardiovascular, respiratory, digestive, oncological, neurological and urological diseases and conditions. Learn and follow us on LinkedIn. 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 We are seeking a Senior R&D Engineer on a permanent basis to join our team. Senior Systems Engineer About the role: We are looking for an experienced Senior Systems Engineer to join the Boston Scientific Urology team. In this role, you will contribute technically in developing medical device product systems, including both capital equipment and active implantable, from initial concept through to product launch. Responsibilities also include supporting acquisition and integration activities, providing technical and engineering expertise. The Systems Engineer considers both business and technical requirements to deliver a quality product that meets user needs. You will collaborate with cross-functional teams to balance user expectations, market opportunities, and business objectives. In this role, you will lead engineering efforts to develop high quality, complex medical device systems including active implantable products, capital systems, combination medical devices, single use devices and software-only products for market differentiation and growth within Urology franchises. Your responsibilities will include: Support acquisition and integration activities for complex capital equipment and active implantable product systems. Provide due diligence support through technology evaluations, gap assessments and remediation planning including partnership with cross-functional teams. Support systems requirements and design modifications needed for seamless integration of product systems. For new product development, work with all stakeholders to translate user needs into design requirements (e.g. hardware, software, mechanical, electrical, cloud interface, etc.) consisting of system requirements, sub-system requirements, product/system security requirements, and system interface requirements to define the system as a whole and all associated sub-systems. Support system architecture, design and integration of new or next generation technologies/products (implantable & capital platform eco-systems) under BSC quality system in collaboration with technical/cross-functional stakeholders. Provide systems thinking perspective for system/sub-system definition and understand how product changes affect the larger system Identify technical risks, develop risk burndown plans, and implement phased system integration approaches, characterization studies to mitigate risk. Support special studies on subjects such as improving system quality, usability, system partitioning, trade off assessments etc. by researching and analyzing options for implementation. Analyzes system requirements to determine testability, completeness and support system test development, systems characterization, test method development and build traceability. Contribute to system risk assessment activities, Use/Design FMEA's activities. Support product/feature design, concept generation and functional prototyping for systems and associated interfaces. Act as an R&D representative on cross-functional deliverables. Create and support documentation as part of the Product Development Process (PDP) and Quality Management System. Collaborate with R&D, regulatory, quality, project management teams for integration activities and communicate findings/recommendations to senior leadership and key stakeholders Builds Systems Engineering capability by mentoring engineers in engineering activities/methodologies and domain knowledge. Required qualifications: Hons bachelor's degree or MSc in electrical engineering, mechanical engineering, biomedical engineering or related field 5+ years of experience with product development activities, preferred in a regulated environment. Experience with requirements authoring design, trade-off analysis, systems integration, risk management and V&V processes. Proficiency in technical documentation, risk assessment and design control processes. Knowledge of System Architectures and design principles. Experience using configuration management, test management, requirements management, and issue tracking systems. Ability to lead teams through a structured approach to solving complex technical problems. Strong knowledge of Design Controls & Risk Management practices Strong personal credibility & excellent communication skills Ability to work cross-functionally and communicate technical insights effectively Preferred Qualifications & Experience Experience leading product development teams in a Medical Regulated Environment. Experience in building and modifying System Architectures, Systems Requirements, Systems Design for implantable medical devices and connected platform eco-systems. Knowledgeable in Human Factors and Usability Engineering processes as part of regulated product development. Demonstrated ability to interact with and influence key stakeholders both internal and external to the organization. Experience dealing with regulatory questions from FDA, BSI, TUV 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 We are seeking a Production Manager on a defined term (18 months) basis to join our team. Job Purpose: Manages a discreet business unit through Production Team Leaders and Support Teams. Primary job functions include: developing capacity plans; managing financial budgets and setting aggressive department goals that support BSC's current and future objectives; partnering with Logistics, Engineering, Quality, HR and Finance to optimize business performance; supporting process development endeavours; ensuring and championing department adherence to Quality regulatory and GMP requirements. This position is responsible for directing and co-ordinating all the manufacturing operations for the area of responsibility. Key Responsibilities: Leadership: a key leader in the value stream, ensuring a team of 200+ produce strong business results and team ethos. Sets stretch goals and ensures strong overall performance. Drive for results/ Customer Focus: leads team to ensure a strong focus on execution, to ensure customer needs met, through delivery of a balanced scorecard across safety, quality, service, cost & people. Able to meet targets & deadlines. Collaborative relationships: forms strong collaborative relationships with Engineering & Quality Manager peers. Develops strong raporte with local and global customers/ support functions. People Management: manages a direct team of Senior Production Supervisors & Production Supervisors, and indirectly manages a team of Product Builders across multiple shifts. Fosters strong employee engagement & communication. Planning & Prioritisation: plans resources and capacity of value stream to deliver on committed build plans and future growth. Coach/ Mentor: coaches & mentors reports to ensure they develop the skills required for their roles, and there is reports to ensure strong succession pipeline in place. Diversity & inclusion: focuses on developing a culture of diversity & inclusion within value stream teams. Financial Acumen: develops an understanding of key financial metrics and levers. Able to manage within budget, and develops annual budgets to deliver on strategic plan. LEAN/ Innovation: promotes the use of key lean tools such as Daily Accountability, 5S, Continuous Improvement, 6 Step Problem Solving and Communication Huddles. Uses innovative thinking to develop new approaches to issues as required. Quality System: ensures strong quality focus from team, in line with Boston Scientific Quality System to ensure patient safety and product/ process compliance. Strategic Thinking/ Execution: partners with Engineering & Quality Manager peers to develop and deliver 3 year strategic plan for Value Stream. Supports and leads site and functional strategic initiatives as required. Preferred Education & Experience: Bachelor Degree (HETAC level 8) in a Business/Engineering or other related discipline. Ideally 8 + years experience in a Leadership role within a manufacturing environment. Excellent leadership skills and demonstrated ability to build strategic relationships. Results driven with a proven ability to deliver targets and meet deadlines. Key Decision Maker and ability to drive innovation and engagement. 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 We are seeking a Quality Manager on a permanent basis to join our team. Job Purpose: Demonstrates commitment to the Quality Policy (patient safety and product quality) through their daily execution of sound quality practices and the maintenance of an effective quality system. Understands and complies with all the regulations governing the quality systems. Ensures their team are aware of their commitment to patient safety and product quality, are current with their training requirements and that they understand and comply with all other regulations governing their work. Key Responsibilities: Develops and manages a high performance quality engineering team with focus on customer needs, compliance, product quality, and risk mitigation. Has the responsibility and independent authority to make decisions related to product quality, including the disposition of non-conforming product. Participates in Customer Complaints investigation for areas under their control. Is viewed as a leader or expert in the areas of QSR and ISO/MDD standards within ones own group, constantly promoting awareness of best industry practices and making appropriate decisions on a daily basis using the Site QA Director as the final arbitrator on critical quality decisions. Develops, directs and executes plans for major segments of complex projects from a quality perspective. Reviews and approves operational, test and validation data to establish technical specifications and performance standards for newly designed or modified products and processes. Takes a leadership role in developing and implementing new techniques and initiatives to enhance the Quality management system on site and across the Corporation where possible. Is key to developing staff on new quality initiatives and assists understanding and rollout of quality initiatives across the department/site. Is a champion of continuous improvement with particular focus on product quality through six sigma initiatives. Is an effective people manager resulting in a motivated high performance team. Is an influential team member, fully motivated to achieve and demonstrate best practices in line with the department. Works with EHS to identify significant environmental impacts of Boston Scientific operations and to establish goals and targets around significant environmental impacts. Works with Production Unit Manager and Engineering Manager to deliver business goals & objectives Is familiar with the internal auditing process. To establish and support a work environment of continuous improvement that supports BSC's Quality Policy, Quality System and the appropriate regulations for the area. What we are looking for: Level 8 Honours Degree in a relevant discipline A minimum of 8 years' experience with progressive leadership responsibilities within a Medical device Quality System regulated organization Experience in Operations Quality required, experience in product transfers and product development and advantage Good technical capabilities, communication skills, teamwork abilities and initiative Proven ability to work well as part of a team & on own with minimum supervision 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.
