Jobs in Ireland

Our Graduate Programme is designed to accelerate your professional development and provide you with extensive experience within Boston Scientific Clonmel. Throughout the 23 month programme, you will be provided with dedicated mentors and will have professional development 1:1 meetings to provide you with a solid foundation for a successful career. Our Graduate Programme is created around hiring the most innovative and best individuals, while Boston Scientific Clonmel provides the means for you to continuously learn and enhance your skill set to drive your career growth.

Responsibilities

• Works as part of the Global Team to assist in creation and monitoring of project plans, communication and documentation of ways of working (standard processes).
• Works on the Global Implementation of a new Enterprise Resource Planning (ERP) tool SAP S4 HANA.
• Works in the JIRA system to update data on project progress
• Works using Agile & Waterfall project management tools
• Conducts her/ himself as a regular full-time member of the staff by accepting and adhering to Boston Scientific's rules and regulations and by engaging in professional and personable conduct at all times with staff and customers. The intern is also obligated to comply with any confidentiality and professional policies established by the Boston Scientific.
• Becomes knowledgeable about her or his own responsibilities and the business and operational issues inherent in them as well as about the Boston Scientific's management and particular issues relevant to the Company.
• Contributes to the preparation and production of proposals and reports by using word processing, spreadsheets, and other computer programs.

Required

• BSc degree (Honours) in relevant discipline essential.
• Must have graduated within the last two years or in final year of University
• Relevant work experience/ co-op programme completed.
• Eligible to work in IrelandCommunication Skills
• Project Management Skills

** 23 Month Contract ** Closing Date 27th November

Should you require a reasonable accommodation during the recruitment process or after if offered, please let us know.

Advancing possibilities for a brighter tomorrow

Responsible for providing mechanical engineering support in the creation and the development of new medical device products (invasive and non-invasive). Interfaces with Design, Quality and Manufacturing organizations to integrate new products, equipment sets or processes into production.

Responsibilities:

• Researches, develops, designs, and evaluates mechanical and electro-mechanical materials, components, assemblies, processes and/or equipment.
• Conducts feasibility studies to verify capability and functionality.
• Develops new concepts from initial design to market release.
• Maintains detailed documentation throughout all phases of development.
• Working as part of the Process Development group this person will aid design of new equipment for new products & manufacturing.
• Work closely with machine Vendors in order to ensure that the equipment is designed, built & tested according to Boston Scientific specifications and is properly handed over to manufacturing.
• Applies technical knowledge to innovate, design, and develop processes, procedures, tooling and/or automation.
• Executes the functional deliverables associated with the PDP/TDP and Quality Systems.
• Plans, organizes, and conducts all aspects of technical reviews.
• Ensures proper documentation is completed to meet quality systems requirements. (e.g., BOM’s,FMEA’s, etc.).
• Reviews or coordinates vendor activities to support development.
• Demonstrates knowledge and application of Lean methodologies, and process improvement tools in identification and elimination of "waste" process steps and development of efficient, cost effective equipment and processes.
• Demonstrates knowledge and application of Process and equipment validation techniques (IQ, OQ, PQ), FMEA, and associated regulatory requirements and applies this knowledge in the efficient & timely validation of equipment and processes.
• Co-ordinates execution and documentation of validation builds, co-ordinates testing of validation units and the compilation, analysis and reporting of the validation results.
• Demonstrates a primary commitment to patient safety and product quality.
• Understands and complies with all the regulations governing the quality systems.

Qualifications/Experience:

• Hons bachelors degree engineering degree qualification
• 3+ yrs engineering experience in a GMP environment

To search and apply for open positions, visit:

Our Graduate Programme is designed to accelerate your professional development and provide you with extensive experience within Boston Scientific Clonmel. Throughout the 23 month programme, you will be provided with dedicated mentors and will have professional development 1:1 meetings to provide you with a solid foundation for a successful career. Our Graduate Programme is created around hiring the most innovative and best individuals, while Boston Scientific Clonmel provides the means for you to continuously learn and enhance your skill set to drive your career growth.

Responsibilities

• Works on the Global Implementation of a new Enterprise Resource Planning (ERP) tool SAP S4 HANA.
• Works in the JIRA system to update data on project progress
• Works using Agile & Waterfall project management tools
• Conducts her/ himself as a regular full-time member of the staff by accepting and adhering to Boston Scientific's rules and regulations and by engaging in professional and personable conduct at all times with staff and customers. The intern is also obligated to comply with any confidentiality and professional policies established by the Boston Scientific.
• Becomes knowledgeable about her or his own responsibilities and the business and operational issues inherent in them as well as about the Boston Scientific's management and particular issues relevant to the Company.
• Assist in building and maintaining data pipelines that support reporting and analytics in Power BI and Microsoft Fabric.
• Support integration of data from various sources (e.g., Excel, SQL databases, APIs) into usable datasets.
• Help maintain and improve Power BI dataflows, datasets, and visual models under guidance from senior engineer
• Collaborate with data analysts and team members to understand business needs and deliver clean, well-documented data.
• Learn and apply best practices around data quality, documentation, and governance.
• Monitor existing data solutions for accuracy and performance, and contribute to troubleshooting efforts as needed.
• Work with data from enterprise platforms such as JIRA, qTest, Solution Manager, SAP, ServiceNow, Snowflake, AWS, SharePoint, and PowerApps to support reporting and operational dashboards.
• Use Power Automate to orchestrate data ingestion, streamline workflows, and automate routine data tasks.

Required

• BSc (Hons) degree in relevant discipline essential.
• Must have graduated within the last two years or in final year of University
• Relevant work experience/ co-op programme completed.
• Eligible to work in Ireland
• Communication Skills
• Project Management Skills
• Some hands-on experience with Power BI (e.g., coursework, internships, or personal projects), including working with dataflows, DAX, or basic semantic modeling.
• Foundational knowledge of SQL and ability to work with structured and semi-structured data (e.g., JSON, CSV).
• General understanding of data governance principles, data lineage, and metadata — with willingness to learn and apply best practices.
• Exposure to or interest in working with enterprise platforms such as JIRA, qTest, Solution Manager, Snowflake, AWS, SAP, ServiceNow, SharePoint Lists, and PowerApps.
• Familiarity with Power Automate for orchestrating dataflows or automating repetitive tasks is a plus.
• Strong interest in solving problems with data and an eagerness to collaborate with both technical and non-technical team members.
• Ability to manage tasks across multiple projects and adapt in a fast-paced, team-oriented environment.

** 23 Month Contract ** Closing Date 27th November

Job Purpose:

As an experienced Quality Engineer, you will demonstrate commitment to the Quality Policy (patient safety and product quality) through 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. Committed to patient safety and product quality.

Key Responsibilities:

• Takes a preventive approach to Quality Assurance, proactively identifying potential issues.
• Uses strong organisational skills and effective time management to ensure work is completed in a timely manner.
• Effectively prioritises a diverse workload to ensure timely completion of critical tasks.
• Plans and executes both daily tasks and long-term projects to ensure timelines are met.
• Takes a pragmatic and logical approach to challenges faced.
• Explains technical topics clearly to diverse stakeholders through effective communication.
• Promotes a culture of continuous improvement through reflection and factoring in previous learnings.
• Makes informed decisions related to product quality, including dispositioning non-conforming product.
• Evaluates complex quality issues and selects the most appropriate problem-solving tools/ techniques.
• Completes timely scoping and containment of product-related issues when required.
• Documents non-conformances using a high standard of technical writing and detailed understanding of Containment, Disposition, Risk Assessment and Investigation.
• Identifies and drives Corrective Actions when required, to prevent/ eliminate/ facilitate/ mitigate the re-occurrence of non-conformances.
• Reviews Complaints’ signals and completes investigations for individual events/ unfavourable trends.
• Familiar with BSC Quality Systems and ISO/MDD/MDR standards.
• Involved in internal and external audits, including audit facing and presenting processes/ documents to auditors as a subject matter expert.
• Knowledgeable on Risk Management, Design Outputs and product/ process Risk Documentation.
• Uses appropriate statistical tools for sampling, capability, trend analysis, and control charts. Effectively interprets and presents conclusions drawn.
• Participates directly in a new product/technology transfer, ensuring compliance to all internal and regulatory requirements.
• Uses knowledge of Six Sigma, Statistical Analysis and Lean Principles to solve problems effectively.
• Involved in change control for work instructions, protocols/ reports and technical documents, either as a change owner or quality approver.
• Evaluates new equipment/processes/chemicals for safety and environmental impact/effect, in conjunction with EH&S.
• Completes validations for processes/ test methods in line with requirements and best practices.
• Maintains relationships and gives technical guidance to Quality Technicians.
• Deals with suppliers, other engineering disciplines within and outside of the site as required.

Education & Experience:

• A Level 8 Degree (240 Credits) or equivalent in a STEM discipline.
• A minimum of 5+ years relevant experience, ideally within the Medical Device industry or another highly regulated environment.

To search and apply for open positions, visit:

Job Purpose:

You will demonstrate commitment to the Quality Policy (patient safety and product quality) through your 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. Committed to patient safety and product quality.

Key Responsibilities:

• Takes a preventive approach to Quality Assurance, proactively identifying potential issues.
• Uses strong organisational skills and effective time management to ensure work is completed in a timely manner.
• Effectively prioritises workload to ensure timely completion of critical tasks.
• Plans and executes daily tasks to ensure timelines are met.
• Takes a pragmatic and logical approach to challenges faced.
• Explains technical topics clearly to diverse stakeholders through effective communication.
• Promotes a culture of continuous improvement through reflection and factoring in previous learnings.
• Makes informed decisions related to product quality, including dispositioning non-conforming product.
• Evaluates complex quality issues and selects the most appropriate problem-solving tools/ techniques.
• Completes timely scoping and containment of product-related issues when required.
• Documents non-conformances using a high standard of technical writing and detailed understanding of Containment, Disposition, Risk Assessment and Investigation.
• Identifies and drives Corrective Actions when required, to prevent/ eliminate/ facilitate/ mitigate the re-occurrence of non-conformances.
• Familiar with BSC Quality Systems and ISO/MDD/MDR standards.
• Involved in internal and external audits, including audit facing and presenting processes/ documents to auditors as a subject matter expert.
• Knowledgeable on Risk Management, Design Outputs and product/ process Risk Documentation.
• Involved in change control for work instructions, protocols/ reports and technical documents, either as a change owner or quality approver.
• Maintains relationships and gives technical guidance to Quality Technicians.
• Deals with suppliers, other engineering disciplines within and outside of the site as required.

Education & Experience:

• A Level 8 Degree (240 Credits) or equivalent in a STEM discipline.
• A minimum of 3+ years relevant experience, ideally within the Medical Device industry or another highly regulated environment.

To search and apply for open positions, visit: