Quality Assurance Specialist Job Opportunity
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About the Role:
A Senior Medical Device Quality Engineer is Required for a Leading Engineering Firm.
This role focuses on ensuring product and process quality for medical devices align with global regulations. A minimum of five years' experience in regulated industries, including strong knowledge of CAPA, validation, and regulatory standards is required.
Main Responsibilities:
1. Supporting new product introductions to ensure seamless integration into production workflows while maintaining compliance with industry standards.
2. Liaising between teams to lead investigations and facilitate effective problem-solving strategies.
The investigator must have excellent analytical skills and be able to make informed decisions based on available data. They will also need strong communication skills to effectively convey findings and recommendations across all levels within an organization.
The engineer should also focus heavily on mentoring junior team members in areas such as best practices adherence when conducting audits or training workshops designed specifically around auditing techniques related primarily towards achieving ISO certification requirements through successful internal audits performed internally throughout different departments company-wide leading collaborative environment approach management principles!