Overview:
The Design Quality Engineer II plays a pivotal role in ensuring that new product designs and manufacturing processes meet all regulatory standards.
About You:
* You will have a third-level qualification in engineering, science, or a technical field.
* A minimum of five years of experience in the medical device or pharmaceutical industries is required.
Your Key Responsibilities:
1. Represent quality interests and concerns on project teams.
2. Lead risk management activities and own quality engineering tasks for NPD projects.
3. Review design control compliance requirements and initiate corrective actions as needed.
4. Support biocompatibility testing aligned with ISO 10993 and participate in internal and supplier audits.
Preferred Skills:
* Attention to detail
* Adaptability
* Strong problem-solving abilities
* Excellent interpersonal skills
We are seeking an experienced professional who can effectively manage multiple projects independently while collaborating with team members and meeting deadlines consistently.