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QC TEAM LEADER (PTX)

 

Company:

COOK MEDICAL

Job Reference Number

14571220

Client ID:

RI/QCTL

Posted On:

Feb 20 2012

Location:

MUNSTER, LIMERICK

Job Type:

Permanent

Salary:

NOT DISCLOSED

Benefits:

  • SPORTS & SOCIAL CLUB
  • FLEXITIME
  • SUBSIDISED CANTEEN
  • CAR PARKING
  • PENSION / PRSA
  • EMPLOYEE ASSISTANCE PROG
  • QUINN HEALTHCARE
Primary Function


The primary function of this role is to work with the QC Supervisor to coordinate daily workflow within IQC, FQC and PKQC, ensuring that all product, which is manufactured in or distributed by Cook Medical, is tested appropriately and passes specified quality control requirements before being shipped to customers.


Responsibilities

    Monitor level of work in the area ensuring that there is sufficient work available at all times and that set targets are achieved.
    Carry out day to day QC duties as required.
    Act as first point of contact for team members on quality control issues/queries which have been escalated by the QC team.
    Ensure that new employees receive induction training and that Induction Training records are returned to HR when they are completed.
    Ensure that training of new employees or employees being trained on a new product is completed in a timely manner.
    Work with team members to identify areas in which the person may require training or retraining.
    Be familiar with company Quality procedures and instil a Quality ethos to team members.
    Be familiar with company safety policy and take an active part in assisting the company to provide a safe working environment.
    Discuss employee performance with area Supervisor/Manager prior to review.
    Ensure all internal communications are made available to members of the QC team.
    Follow company procedure on Holiday Requests.
    Produce and verify time sheets. Give the time sheets to the QC Supervisor for final approval.
    Compile Monthly Reports based on thru-puts/rejects in the area.
    Originate Change Requests for QC documents.
    Originate Deviation Requests if required.
    Work with the Quality Control supervisor in relation to rejects from IQC and Production for the Materials Review Board.


Requirements


    Experience in a manufacturing environment.
    Previous experience in medical devices, while not essential is advantageous.
    Previous experience working in a Team Lead/Supervisory capacity is advantageous
    Good communication and inter-personal skills.
    Ability to work as part of a team.
    Some flexibility as regards working hours / days.