Description
I have an immediate opening for a Quality Senior Supervisor (Salary €60K- €70K) with a leading medical device company based in Wexford.This is an excellent opportunity for senior quality professionals looking to make the step up into management position in a role that will oversee the supervision of up 25 engineers/inspectors.
The Quality Senior Supervisor will primarily be responsible for maintaining and improving where necessary all quality systems and monitoring production process for compliance to implemented process controls.
Responsibilities:
* Developing and maintaining quality world class systems related to the manufacture of guide wires while developing employee efficiencies,
* Direction for quality in all manufacturing areas
* Direction of the relevant quality engineers in areas of responsibility
* Direction of the relevant inspectors in areas of responsibility
* Playing a role in the plant annual objectives.
* Ensure continued compliance with all Regulatory Standards including:
-ISO 13485, -FDA QSR,-ISO 14000
* Monitor production process for compliance to implemented process controls to ensure quality product is shipped to customer and provide:
-Trend analysis of data from the controls
-Potential improvements for review with engineering based on the trends.
-Areas for Improvement to management.
* Support the RCA meetings to ensure that internal and customer concerns are handled and dealt with in an appropriate manner.
* Review and ensure that for areas of responsibility
* Develop and maintain a program ensuring only correctly validated equipment is used in production process. This will include:
a.Participation in validation protocol development
b.Overseeing completion of validation or validation samples
c.Supporting the manufacturing engineering function to ensure compliance to related element of quality system.
* Supervision of quality engineers to ensure compliance for their areas of responsibility.
* Project meeting attendance as required.
* Attend and participate in daily cell meetings.
* Ensuring information for PMR and Management Review meetings is maintained and available on time.
* Ensuring all quality reports are of required standard and issued on time.
Requirements:
* Engineering or science Degree preferably with Quality Engineering included.
* 5 years medical device experience
* Previous Supervisory/management experience
* Ability to communicate and work with people inside and outside the department.
* Good communicator (written and oral).
* Ability to train and lead.
* Ability to co-ordinate, plan and organise in a timely manner.
* Knowledge of engineering theories and methods
This is an fantastic opportunity to join a very progressive company in the South East. If you are interested in hearing more about this position please respond directly to this advert or contact Derek Sheridan on for further details.