Job Title: Quality Inspector – Documentation Control
We are seeking a full-time Quality Inspector – Documentation Control to support our team.
Responsibilities:
* Inspect incoming materials and finished products for quality, ensuring compliance with regulatory standards and practices.
* Perform environmental monitoring and document results in accordance with EN ISO 13485 and FDA 21 CFR 820 guidelines.
* Conduct problem-solving, audits, and update QA documentation to maintain accurate and up-to-date records.
* Support Quality Engineering and Operations by reviewing and managing quality documentation.
Requirements:
* Leaving Certificate + 3 years' medical device assembly experience.
* Proficient computer and documentation skills, including the ability to read drawings and multitask.
* Knowledge of EN ISO 13485 and FDA 21 CFR 820 regulations.
* Ability to work independently with strong organizational skills and attention to detail.
* Forklift license (advantage).