Lead Manufacturing Technician - Evening Shift

Edwards; Limerick; Hybrid; EUR 50,000 - 70,000; Full time

Job summary

Edwards Lifesciences in Ireland is seeking a Lead Technician to provide technical and function-specific knowledge to support Operations and Engineering activities.

The role involves troubleshooting, preventive maintenance, equipment validation, and collaboration with Quality to drive continuous improvements in a sterile manufacturing environment.

This is a hands-on, leadership-oriented position requiring a recognised trade or higher qualification and at least six years of related experience.

Qualifications

• A recognised trade qualification or relevant third-level qualification; plus manufacturing, engineering, or medical device industry experience.
• Minimum of 6 years of related experience.
• Strong written and verbal communication, problem solving and GDP practices.

Responsibilities

• Troubleshoot and maintain equipment to minimize downtime and ensure validation.
• Lead equipment validation projects and investigations.
• Perform preventive maintenance on complex equipment.
• Collaborate with Quality on corrective actions and EWOs/ENCRs.
• Update documentation in systems (ECRs, SOPs, drawings).
• Coach and guide technicians.

Skills

Troubleshooting

Preventive Maintenance

Documentation skills

Team leadership

Problem solving

Education

Trade qualification

Engineering degree

Tools

JDE

QMS

PLM

CAD software

Job description

Innovation starts from the heart. Edwards Lifesciences is the leading global structural heart innovation company, driven by a passion to improve patient lives. With millions of patients served in over 100 countries, each team makes a meaningful contribution by improving patient outcomes and discovering lasting solutions for unmet patient needs.Our Lead Technician position is a unique career opportunity that could be your next step towards an exciting future.

The Lead Technician provides technical and function-specific knowledge to support Operations and Engineering activities.

Working Hours : Monday to Thursday, 4:30pm-3am (Finish at 2am on Thursdays)

How You'll make an impact

• Troubleshoot and recommend maintenance to limit downtime, to keep production on schedule, and to ensure ongoing validation compliance
• Design, set-up and execute feasibility studies, experiments, and tests - both creating and following established protocols - to develop findings for the validation and improvement of equipment and manufacturing processes/methods based on engineering principles; analyze results, make recommendations, and develop reports for Engineering review
• Lead projects related to new equipment validation, equipment investigations, testing, objective evidence of product dispositions and rework
• Perform both scheduled and unscheduled preventive maintenance routines on a wider range of complex equipment to validate user operation and avoid program down time
• Check for failures in more complex equipment and processes, and perform corrective actions to affected areas that have down time, including conducting and writing impact assessment reports of incidents
• Collaborate with Quality in devising and implementing corrective actions, exception work orders (EWOs), Equipment Non-conformance Reports (ENCRs), and Out of Tolerance (OOTs)
• Review documentation and take appropriate actions to ensure that information is appropriately catalogued and follow through to validation and qualification of equipment, including transferring information to appropriate locations, e.g., ECRs, SOPs, drawings, and tooling, for Engineering approval
• Utilize manufacturing software (e.g., JDE, QMS,PLM) to update documentation in systems
• Collaborate with Engineering and CAD/Designers to develop new basic tools
• Provide coaching and guidance to technicians
• Other incidental duties

What you'll need (Required):

• A recognised trade qualification or relevant third-level qualification, plus relevant manufacturing, engineering, or medical device industry experience;
• A minimum of 6 years of related experience.

What else we look for (Preferred):

• Strong written and verbal communication, interpersonal, and relationship building skills
• Problem solving methodology, root cause analysis, and GDP (Good Documentation Practices)
• Strong computer skills, including usage of MS Office Suite; and CAD if applicable
• Full knowledge of validation and improvement of automated equipment
• Ability to troubleshoot manufacturing equipment
• Knowledge of material compatibility in the proposed use environment
• Ability to understand the fundamentals of project management
• Full knowledge routine preventive maintenance of production equipment
• Full knowledge electrical, mechanical, electronic, pneumatic, and controls
• Knowledge of and adherence to Edwards Environmental Health and Safety and Quality guidelines as they relate to department clean room medical device manufacturing
• Knowledge of Good Manufacturing and Good Documentation Practices supporting a medical device environment
• Strict attention to detail
• Must be able to work with other departments including formulating work instructions and providing guidance and training to lower-level employees with little to no direction
• Adhere to all company rules and requirements (e.g., pandemic protocols, Environmental Health & Safety rules) and take adequate control measures in preventing injuries to themselves and others as well as to the protection of environment and prevention of pollution under their span of influence/control