Manufacturing Technician S2 Csp Sterilisation Days Nights jobs at Boston Scientific in Ireland, Galway

Job Purpose:

role. Sterilization operates in a 24/7 shift pattern (12-hour shift).

Note Job shifts:

Day1 Mon to Wed (7AM to 7PM), alternating Sunday

Day2 Thurs to Sat (7AM to 7PM), alternating Sunday

Nights1 Sun to Tues (7pm to 7AM), alternating Saturday

Nights2 Wed to Fri (7PM to 7AM), alternating Saturday

Responsibilities:

• Work with Line Facilitators to manage the process, the process loads and Production Area.
• Work with Manufacturing Engineers in developing, trouble shooting, standardising and improving existing production methods and procedures.
• Work with Engineering team to commission and validate new sterilization equipment.
• Support and assist on equipment and cycle qualifications and validations.
• Proactive on PSPI and PDCA in the area.
• Work on Electronic/ Mechanical troubleshooting and electronic hardware interfacing.
• Investigate and implement new production methods.
• Interface with a variety of BSI personnel and with outside vendors when necessary while performing the above.
• Take responsibility for preventative maintenance procedures with an assigned process or area.
• Assists in implementing technical improvements under the teams C.I. program.
• Communicates any concerns about work process regarding environmental impact, health or safety issues to their manager.
• Owns the key performance metrics for the ME function.

Qualifications and Experience

• HETAC NFQ Level 6 Honors Degree in STEM
• Sterilization experiences an advantage.
• Strong focus on safety and safety procedure adherence.
• Strong electromechanical experience required.
• Plant equipment experience an advantage.
• Electrical level 2 or 2+ years relevant years experience required
• Comfortable working with full PPE (respiratory gear etc) – requirement to be clean shaven
• Experience with Gas cylinders an advantage
• Drives continuous improvement efforts
• Good technical capabilities, communication skills, teamwork abilities and initiative.
• Proven ability to work well both as part of a team but also able to work on own with minimum supervision

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Job Purpose

In Operations, provide daily support of products, processes, materials, and equipment to achieve production goals (i.e., quality, delivery, cost, productivity, and safety).

Key Responsibilities

• Uses problem-solving methodologies to support issue investigations and make improvements.
• Actively interacts with cross-functional team members through face-to-face meetings, virtual video calls, emails or group sessions.
• Practices good teamwork by actively listening, sharing ideas and working together as one team, in support of day-to-day operating requirements.
• Assists in the development and analysis of process, product, material or equipment specifications and performance requirements
• Evaluates new equipment/processes/chemicals for environmental impact to eliminate or lessen such impacts in conjunction with Environmental Health and Safety (EHS)As part of personal development, may assume engineering responsibility for manufacturing equipment or processes within the cleanroom environment.
• Interfaces with vendors, possibly physicians and other technical consultants as part of the role.
• Builds Quality into all aspects of work by maintaining compliance to all quality requirements in Standard Operating Procedures.

Education & Experience

• NFQ Level 8 Honours Bachelor’s degree in a STEM discipline is required. (You must be graduating prior to September 2026 or have graduated in last 2 years)
• An understanding of systems and a willingness to learn and develop technical skills.
• Good communication skills, teamwork abilities and initiative.
• Proven ability to work well as part of a team & on own with minimum supervision.
• Eager to learn and active participate.
• Strong interpersonal skills.

• Eligible to work in Ireland.

• Competitive Benefits –we offer market leading benefits including performance-related bonus, pension contribution, onsite gym, onsite parking, subsidised canteen, organised social groups and healthcare.

• – opportunity to transform the lives of patients worldwide.
• Our Culture- our work is guided by core values that define our culture and empower our employees.
• Career Development– our highly engaged leaders will empower you to grow and will invest in your potential. You can also broaden your skills through personal development courses.
• Opportunity to Innovate– we encourage you to fulfil your true creative potential by speaking up with your ideas and solutions to problems that matter.
• Work-Life Balance– we have created a culture that acknowledges, respects and supports your life and work choices.
• Corporate Social Responsibility– we are dedicated to progressing business practices in areas important to our communities. Our onsite charity events have raised over €1.5 million for worthy causes in the past ten years.

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Job Purpose:

Responsibilities that include data analysis and identification of process improvement. The role will span all operations on site and will give the successful candidate a very good understanding of all aspects of the operation Projects will incorporate lean manufacturing, theory of constraints, quick response manufacturing, Just-In-Time, Methods-Time Measurement, or a variety of other systems improvement philosophies.

Responsibilities:

• Preventative Maintenance & Calibrations.
• Continuous improvement of all types of mechanical and electrical systems, to achieve maximum availability and equipment reliability, in a regulated Medical Device facility.
• Update and maintain all maintenance records in an organised and efficient manner.
• Provision of technical support and troubleshooting on automated controls, electrical equipment and mechanical systems.
• Participate fully in training and development in cross-skilling and other job-related competencies.
• Work in compliance with the site Safe Systems of Work including permitting, LOTO, isolations and safety documentation review.
• Work Collaboratively with Operations, Quality, EHS and other departments.
• Any other reasonable duties which may be required by management from time to time

Requirements:

• Completion of Mechanical/Electrical/Multiskilled Apprenticeship or NFQ Level 6 qualification.
• Experience within Medical Devices or a similar industry is an advantage.
• Knowledge of electrical, mechanical, hydraulic & pneumatic drawings would be an advantage.
• Experience of working on & maintaining Electrical and Mechanical equipment within a regulated industry.
• Experience with SAP based Computerised Maintenance Management System and electronic Maintenance Request Systems.
• Excellent interpersonal and communication skills.
• Strong planning and organizational ability.

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Job Purpose:

To perform routine Analytical testing as assigned and to accurately document test results. They are responsible for ensuring that all testing is carried out in line with all quality system and regulatory requirements.

Responsibilities

Key Responsibilities:

• Demonstrate a primary commitment to patient safety and product quality.
• Understand and comply with all the regulations governing the quality systems (including ISO 17025 for accredited laboratory).
• Delivery of key Quality and Performance Objectives.
• Conduct testing according to written procedures, Raw material, in-process and finished product testing in the Analytical laboratory.
• Collect, compile and analyse data and prepare laboratory reports.
• Ensures all notebooks/logbooks/Worksheets are completed and reviewed in a timely manner.
• Records all information and raw data only on designated forms or logbooks and/or via appropriate systems.
• Assist manufacturing/operations/quality in solving quality-related problems.
• Ensures NCE’s, laboratory investigations and out of specification results are documented and reported to Laboratory Management.
• Ensure equipment, standards and other materials are approved/released prior to use.
• Performs cleaning, preventative maintenance, verification of instruments and equipment where required.
• Ensure all training is completed as per Laboratory Training Program.
• Support Internal/External Audits.
• Communicates any concerns about work process regarding environmental impact, health or safety issues to their Manager.
• To build quality into all aspects of work by maintaining compliance to all quality requirements, including Good Manufacturing Practice, Good Laboratory Practice and Good Documentation Practice (GMP, GLP and GDP).
• Perform and assist with additional duties as may be directed by the Supervisor.
• Identify and implement opportunities for improvement.

Education & Experience:

• NQF Level 6 (120 Credits) or above in STEM Discipline.
• Experience and Product Knowledge in Analytical Lab is required.

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Advancing possibilities for a brighter tomorrow

Function:Quality Pre & Post

Reporting to:Associate Quality Manager

Closing Date:18th April 2025

Days

Job Purpose:

You will demonstrate commitment to the Quality Policy through your daily execution of sound quality practices and the maintenance of an effective quality system and complying with regulations governing the quality system. Quality Pre and Post is a sub-group of the site Quality Systems team that supports all material inbound and outbound activities including product release.

Key Responsibilities:

• To provide assistance and support to the Quality Pre&Post function.
• Ensure compliance to all applicable regulatory standards, current GMP procedures and practices
• Review and update of documentation.
• Control of non-conforming product.
• Compile metrics and report results as required to key stakeholders
• Problem solving and continuous improvement investigations.
• To provide assistance and support to the Quality Engineering and Operations function.
• Provision of excellent service to all internal customers for the production group or functional area in which they work.
• Work with Boston Scientific systems including but not limited to eCAPA, MES, SAP, Windchill.
• Communicate any concerns about work process regarding environmental impact, health or safety issues to their Manager
• Raise Quality Catches & implement Mitigations
• Participate in safety walks
• Audit preparation activities

Education & Experience:

• NFQ Higher Certificate Level 6 (120 Credits) or above in STEM Discipline
• Must have 2-4 year experience in a similar role. Medical Device experience is advantageous
• Continuous improvement mindset with a passion for Quality
• Decision making ability coupled with the ability to work on one’s own initiative and with minimum supervision
• Good interpersonal skills and organisational skills
• Excellent attention to detail

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