Job Title
A quality engineer with 5-10 years' experience in med-tech is required to support a remediation program.
The successful candidate will focus on manufacturing process validation, quality system updates, and documentation remediation.
Key responsibilities include:
* Partnering with process owners to capture and remediate issues.
* Supporting process validation and documentation updates.
* Driving CAPA/NCR closure and implementing compliant solutions.
* Providing technical writing for quality and manufacturing documents.
Requirements include an engineering or quality degree, strong technical writing skills, and knowledge of 21 CFR Part 820 and ISO 13485.
Location: Cork