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Siobhan Ryan
Life Science

+353 1 507 9254
[email protected]
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Details

Manufacturing Technician/Operator


Reference:SR - A009579 (AGCE-662048) Location: Limerick City
Qualification:CertificateExperience:0-1 Years
Job Type:PermanentSalary: Not Disclosed
May be suitable for: Manufacturing Engineer, Process Technician

Excellent opportunity to join a dynamic medical devices company as MANUFACTURING TECHNICIAN

Swing Shift Role with hours as follows;

Week 1 - 7.30am to 3.30pm
Week 2 - 3.30pm to 11.30pm


Purpose of the role:

The Manufacturing Technician will utilise their technical and interpersonal skills in supporting the manufacture of medical device products and maintaining process and manufacturing technologies within their area of responsibility.

Key Responsibilities:

Key responsibilities will include (but are not limited) to the following.

  • Ensure Quality and EHS policies and procedures are adhered to always.
  • Work closely with Team Leads to plan and prioritise planned changeovers and equipment setups that occur daily.
  • Ensure where applicable, that downtime and process issues are communicated and handed over between shifts in an effective manner.
  • Demonstrate an attitude of knowledge sharing within the technician group with respect to equipment and processes.
  • Day to Day Manufacturing and Process support, including but not limited to-

    • Support all engineering and Value Stream activities in support of the commercial build plan.
    • When required support and assist new customer development opportunities within the Value Stream.
    • Changeovers & set up of manufacturing equipment and processes.
    • Look after tooling stocks – e.g. heater bands, dies, core pins & pinch offs and other tooling when required.
    • Problem solving of process and manufacturing issues.

  • Work within the technician and wider engineering group in providing solutions to systematic downtime and process issues.
  • Work with the wider group in the Value Stream in identifying opportunities for yield and cost saving improvements.
  • Support CIP project activities within the Value Stream.
  • Updating procedures / docs in line with DCR changes etc.
  • Maintaining a clean and efficient work area (6S) of the technical areas.
  • Re-organisation of tooling storage and tooling control systems.
  • Maintenance of controlled tooling drawings.
  • Liaison with tool suppliers and external contractors.
  • Maintenance of PM schedules as applicable.
  • Ensure full compliance with regulatory requirements.


Professional skills/knowledge
  • Engineering or relevant manufacturing qualification to Certificate level.
  • Good mechanical aptitude to have the ability to problem solve day to day mechanical issues in the production environment
  • Injection moulding experience – knowledge of injection moulding equipment is preferable but not essential.
  • Ability to multi-task.
  • Self-Starter with the ability to work independently with some supervision and with drive and enthusiasm for quality and yield improvements.
  • Work within the Value Stream Team to ensure that product ships to the customer as agreed.
  • Ability to work as part of an effective engineering team.
  • Excellent communication and interpersonal skills.
  • Ability to work with cross functional teams in the Value Stream and wider site.
  • Good problem-solving skills.
  • Willing to learn new skills.
  • Ability to work in a fluid, demanding environment.
  • Understanding and appreciation of company ethics standards.
  • Knowledge and experience of working in the medical devices industry is preferred but not essential.
  • Ability to use interpersonal skills to work with people to successfully deal with day-to-day manufacturing and process related issues.
  • Demonstrates behaviours in line with company Core Values.
  • Ability to contribute constructively at meetings.
  • Understand the key drivers impacting the business.