This job has expired

Quality Inspector - Documentation Control

Employer
Manpower Ireland
Location
Sligo
Salary
Negotiable
Closing date
20 May 2022

View more

Sector
Manufacturing
Job Type
Permanent
Hours
Full-time
You need to sign in or create an account to save a job.

We are currently recruiting for the Quality Inspector - Documentation Control for a medical device engineering company based in Sligo

Responsibilities:
The responsibilities for this position will include the following:

  • Approving incoming materials by confirming specifications; conducting visual and measurement tests; rejecting and returning unacceptable materials.
  • Routine Final QA Product Inspections of finished parts in production by confirming specifications; conducting visual and measurement tests; communicating any non-conformance to Production Manager & Quality Dept.
  • Routine Environmental Monitoring; pressure differential readings, Particulate Monitoring, Microbial Monitoring.
  • Document inspection results by completing reports and logs; inputting data into quality database.
  • Problem solving and continuous improvement investigations.
  • Performing internal audits as required.
  • Review and update of QA Documentation.
  • Providing assistance and support to the Quality Engineering and Operations function.
  • Driving continuous improvement and best practices in QMS "Right First Time".
  • Maintaining safe and healthy work environment by following standards and procedures; complying with legal regulations.
  • Updating job knowledge by participating in educational opportunities.
  • Ensuring compliance to all applicable regulatory standards and cGMP procedures and practices.
  • Other responsibilities may be assigned from time to time as needed, based on the evolution of the company and the requirements of the department/position
  • Reviewing documentation for completeness.
  • Scanning, filing, backing up and archiving quality documentation to maintain company's quality management system.
  • Maintaining and controlling all external supplied documentation which may affect product realisation.
  • Other responsibilities may be assigned from time to time as needed, based on the evolution of the company and the requirements of the department/position.

Other such duties as may be assigned from time to time by their Manager.


Person Specification:
Candidates likely to be called for interview will have most or all of the following:
* Leaving Cert plus minimum 3-year Medical Device assembly experience.

* Proficient computer skills. * Understand general principles of EN ISO 13485 & FDA 21 CFR 820.

* Competent in Inspection method and reading drawings and specifications. * Decision making ability coupled with the ability to work on one's own initiative and with minimum supervision is required, and ability to multitask and prioritise. * Good interpersonal skills and organisational skills.

* Excellent attention to detail.

* Documentation skills.

* Competent in inspection methods and reading drawing and specifications.

* Understand the principles of product/parts and FIFO.

* Communicates any concerns about work process regarding environment impact, health or safety issues to their manager.

* Forklift Licence would be an advantage.


Position Details
This is a full-time position on a Permanent contract.

You need to sign in or create an account to save a job.

Get job alerts

Create a job alert and receive personalised job recommendations straight to your inbox.

Create alert