Sector: Medical Devices Type: Permanent
Contact: Matt Henocq Job Published: 1 day ago
Quality Engineer
As a Quality Engineer, you will support the local quality management system and processes. You will act as an advocate of Quality, promoting the group's vision and mission while supporting the overall business goals. You will collaborate closely with teams in areas such as Supplier Quality, Manufacturing, Order Fulfillment, and Regulatory Affairs.
Responsibilities
1. Complete projects and compliance activities.
2. Prepare monthly metrics related to your area of responsibility.
3. Analyze process data and trends to drive optimization and improvement.
4. Represent the QA organization in processes like CAPA, Order Fulfillment, Manufacturing, and Deviation Management.
5. Support other QA and functional teams on technical issues to achieve results.
6. Participate in external audits by regulatory authorities.
7. Promote and uphold company values.
8. Prepare internal audit plans, conduct audits, and compile audit reports.
Required Skills and Experience
* Bachelor's degree in engineering or a related field, or a formal engineering apprenticeship with relevant experience.
* Training and experience in medical device regulatory standards (e.g., ISO, IEC, MDR, MDSAP).
* Lead auditor trained in ISO 13485/9001.
* Proven experience in Quality, Regulatory, or Engineering roles within a medical device environment.
* Strong communication skills, both written and verbal, with effective teamwork abilities.
* Objective-driven and customer-focused mindset.
* Ability to work independently and produce results.
* Professional integrity and the ability to translate regulations into business requirements.
* Structured problem-solving skills with knowledge of quality tools and techniques.
Services advertised by Gold Group are those of an Agency and/or an Employment Business. We will contact you within 14 days if selected for an interview. For our privacy policy, please visit our website.
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