Quality , Science, Pharmaceutical & Food
Quality Tech -Med Device
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Contract
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Sligo, County Sligo, Ireland
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42132567
Desired Skills: incoming quality,quality tech,qa technician
PE Global are currently recruiting for a Quality Technician for our Medical Device client site in Sligo on a 12-month initial contract:
QUALITY TECHNICIAN MEDICAL DEVICES
Job Dept: Quality Assurance
Responsibilities
- To work as a member of the Quality Team to ensure that Quality goals and objectives are achieved.
- Ensure that all actions comply with current good manufacturing practices.
- Operate within the QC/ IQA and Metrology Areas, as required.
- Complete incoming product testing per the relevant approved specifications and procedures.
- Complete in-process and final release product testing per the relevant approved specifications and procedures.
- Ensure Management is kept informed of all Quality Events or potential Quality Events Related to the product or process.
- Ensure all Quality System documentation is thorough, complete, and compliant.
- Audit the quality system with other personnel where required.
- Support Change Management Process including Product and Quality System document review and updates.
- Generate and Providing metrics for inclusion in the management review, monthly reports and overall Quality Performance
- Ensure compliance with training requirements is maintained.
- Participation in continuous improvement programs to implement improvements in the quality, safety, environmental and production systems at the site.
- Generate batch records for as required in support of manufacturing process orders.
- Complete disposition decisions for incoming material
Essential Requirements
- A third level qualification in an appropriate discipline is desirable.
- 2+ years’ Experience within a regulated GMP environment is desirable.
Experience Required
- 1 year plus experience in the day-to-day operation of the quality system in a highly regulated combination product/device manufacturing environment is desirable.
- The position requires a high level of attention to detail and mental concentration, to ensure total compliance with operating procedures and Regulations at all times.
- The position requires the ability to adapt to new processes on a regular basis.
- The position requires total commitment to quality and safety at all times.
- Has a personal responsibility to commit to the Vision, to engage and align with the Strategic Imperatives, and to consistently execute in accordance with the Operational Pillars and Ways of Work
- Requires good knowledge of Company Policies and Procedures and involves. working towards general results to achieve organizational needs.
- Demonstrates an ethos of Right First Time at all times.
- Adheres to and follows all procedures policies and guidelines ensuring compliance with cGMP and ISO/FDA regulations and company policies, procedures, and guidelines.
- Shows a high level of attention to detail and tenacity to ensure any issues noted are elevated to the Operations Quality Team Leader.
- Complies with cGMP at all times.
- Considerable and continual care and attention to detail is needed to detect and avoid errors.
Interested candidates should submit an updated CV, marked for the attention of Audrey
audrey.mccarthy@peglobal.net or 00353 21 4297900
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