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Quality Systems Technician (Spiddal Galway)
Location: Spiddal, Galway, Ireland
Job Category:
Other
EU work permit required:
Yes
Job Reference:
7b8a758fe620
Job Views:
192
Posted:
03.03.2025
Expiry Date:
17.04.2025
Job Description:
At Integer, we create a culture that unifies and embraces the uniqueness we all bring to the company, positioning us for long-term success.
REPORTING STRUCTURE
The Quality Systems Technician will report to the Quality Supervisor.
ROLE
As Quality Systems Technician, you will actively support quality systems and compliance activities including review and maintenance of documents, records and data, support for audit preparation and execution activities, Non-conformance reports, Corrections, Corrective & Preventive actions within area of responsibility, and continuous process improvement.
RESPONSIBILITIES & DUTIES
* Compliance to applicable regulatory standards and current GMP procedures and practices.
* Maintain QS documentation and records in a compliant state.
* Support/maintain the document and record control processes.
* Support and actively participate in audits (internal and external) and follow-up activities.
* Complete/Support administrative review for Complaint/Manufacturing Investigations.
* Initiate and process Engineering Change Notices for document updates.
* Actively support activities associated with the Supplier management process.
* Participate in the initiation and implementation of Non-conformance reports, Corrections, Corrective & Preventive actions within area of responsibility.
* Participate in continuous process improvement initiatives.
* Collate/trend and present Key Performance Indicators and Quality data to support communications and Management review.
* Participate in training events to continuously develop and maintain competencies.
* Respond to non-standard requests from customer needs.
* Support quality system compliance activities including review of standards and follow-up to ensure satisfactory closure of identified gaps.
* Act as a Trainer for responsibilities associated with Quality Systems and document control.
* Provide support for document control activities and personnel.
* Perform other related duties as assigned by Quality leadership.
EDUCATION & EXPERIENCE
Minimum of 2 years’ experience working within the Medical Device/Pharmaceutical Industry.
Previous work experience within QS/QA/QC environment.
Knowledge of Medical device Regulatory requirements (e.g. ISO13485, FDA QSR 21CFR Part 820).
Level 7 or 8 Degree in Manufacturing/Quality Engineering/Life Sciences.
Capabilities & Abilities:
* Knowledge of and adherence to Quality systems.
* Good computer skills in usage of MS Office Suite - Microsoft Word/Excel/PowerPoint.
* Proficiency with Electronic QMS systems (e.g. SharePoint, Reliance, etc).
* Ability to work on own initiative as well as part of a team.
* Good documentation skills with strict attention to detail.
* Logical and methodical approach to work practices and processes.
* Strong written and verbal communication skills are essential.
* Basic understanding of statistical techniques.
* Resilient to deal with challenging situations.
* Capable of influencing change.
* Highly motivated.
* Self-aware/Optimistic/Empathetic.
U.S. Applicants: EOE/AA Disability/Veteran
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