Skip to main content
Cook Group

Cook Medical jobs in Limerick, County Limerick

Post your CV and find your next job on Indeed!

Cook Medical jobs in Limerick, County Limerick

Sort by: -
    • Proven knowledge and experience (ideally minimum 6 years) of working with ISO, EU, FDA medical device standard regulations.
    • View all Cook Group jobs - Limerick jobs - Quality Engineer jobs in Limerick, County Limerick
    • Salary Search: Team Lead, Quality Engineering salaries in Limerick, County Limerick
    • See popular questions & answers about Cook Group
    • Provide proficient technical training and support to medical personnel on the use of Cook’s medical devices as required.
    • Maintains an excellent understanding of the global medical device regulations.
    • Knowledge of medical device quality standards/practises or similar regulated…
  • View similar jobs with this employer
    • Minimum of 10 years experience in an advanced manufacturing environment, medical device field preferred.
    • Partnering closely with IT, the successful candidate…
    • Experience of medical device development from concept through to commercialisation.
    • Knowledge of relevant ISO, EU, FDA medical device standards regulations is…

People also searched:

cook medical jobs
zimmer biomet
medical secretary, administration
cook medical
kitchen
kitchen assistant
medical administration
medical receptionist

Job Post Details

Team Lead, Quality Engineering - job post

Cook Group
3.3 out of 5 stars
Limerick, County Limerick
Full-time
You must create an Indeed account before continuing to the company website to apply

Job details

Job type

  • Full-time

Location

Limerick, County Limerick

Full job description

Overview:
The primary function of this role is to lead and supervise the Quality Engineering group including Senior Quality Engineer(s) and Quality Engineers. Agree objectives, generate training plans, coach team members, carry out performance appraisals and deal with performance related issues. Assess workload for the group and allocate tasks accordingly.

Reporting to: Quality Engineering Manager

Find out more about Cook Medical here
Responsibilities:
  • Drive all assigned Quality Engineering projects and ensuring that they are managed in a structured fashion and completed in compliance with the relevant procedures.
  • Manage and drive project activities to ensure timely completion of project milestones.
  • Represent team at key review meetings.
  • Work closely to build effective relationships with other functions in particular Operations, IT, Engineering and Regulatory teams.
  • Leading the area of FDA, QSR and ISO13485 requirements, promoting, awareness of best industry practice and making appropriate decisions on a daily basis using the Quality Engineering Manager as the final arbitrator on critical quality decisions.
  • Identify and implement opportunities for improvement.
  • Maintain a proactive approach to developing Cook’s Quality system to meet the changing needs of the business.
  • Ensure that in-house or external Quality issues are effectively prioritised and acted upon in a timely manner.
  • Responsible for Quality systems including the following key processes within the Quality Engineering group:
    • Design, Process and Software Validation.
    • Supplier Quality.
    • CAPA.
    • Non conformances.
  • Support of the Internal Audit, Supplier Audit and Regulatory Audit Programmes.
  • Prepare execute and analyse Quality Engineering Documentation.
  • Trending and analysis of key Quality metrics.
  • Responsible for the assessment of risk throughout Quality Engineering key processes and systems.
  • Provide leadership and mentoring to team members to ensure the effective completion of activities associated with their role.
  • Designee for the Quality Engineering Manager.
  • The Quality Engineering Team Leader signature is equivalent to Senior Quality Engineer.
  • Ensure that Cook’s Code of Conduct is considered with in all business matters carried out on Cook’s behalf.

Qualifications:
  • Third level qualification in Science, Engineering or relevant technical discipline.
  • Proven knowledge and experience (ideally minimum 6 years) of working with ISO, EU, FDA medical device standard regulations.
  • Previous supervisory experience would be beneficial.
  • Excellent communication and inter-personal skills.
  • Proven track record of perusing continuous self-improvement.
  • Good working knowledge of Microsoft Office.
  • Proven Problem-Solving Skills.
  • Good working knowledge of statistics.
  • Knowledge and experience of all aspects of validation.
  • Excellent organisational, time management and presentation skills.
  • Excellent attention to detail.
  • Proven self-starter
  • Willingness and availability to travel on company business.
Let Employers Find YouUpload Your Resume