hirly

Edwards

Lead Manufacturing Technician - Evening Shift

Ireland-Limerick

See how you match this job — and similar ones. Free.

Upload your resume and hirly scores it against this role at Edwards first, then against similar open jobs, and shows where you fit and why.

PDF or DOCX, up to 12MB. No sign-up to see your matches.

Get past the screening software and onto a recruiter's desk

hirly rewrites your resume for this job — matching the keywords and skills in the posting, moving your most relevant experience to the top, and writing a cover letter to fit. About 30 seconds.

  • Keywords matched to this posting
  • Fit score before you apply
  • Cover letter included
Tailor my resume for this job →

Apply from your AI assistant

Connect hirly to Claude and ask it to apply to this job. hirly tailors your resume, fills the employer’s form and asks before sending. ChatGPT: manual setup today.

Some employer sites stop an application at a CAPTCHA or sign-in and hand it back with a link. Applying needs a paid plan. Works with any assistant that supports MCP.

hirly's read of this role

Seniority
Lead / management
Country
IE
Work mode
On-site / unstated
First seen by hirly
14 Oct 2026

Derived automatically from the posting. Upload your resume above to see how the role scores against it.

the posting

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 of 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
Original posting on Edwards's site ↗

Listed on hirly, a job board. hirly is not the employer: Edwards is hiring for this role.

Browse similar roles

Want this one?

Upload your resume and hirly rewrites it for this job and writes the cover letter — in about thirty seconds, before you sign up.

Tailor my resume for this job