Are you ready to push the boundaries of global health and make a lasting impact, this role within a well-established Medical Technology company could be your next best move.
Hobson Prior is seeking a proactive Manufacturing QA Engineer to ensure high-quality production standards in medical devices. You will focus on maintaining compliance, improving processes, and supporting manufacturing quality across internal and external operations. This role is essential for sustaining quality and regulatory standards as we expand our market presence.
Please note that to be considered for this role you must have the right to work in this location.
Responsibilities:
- Oversee quality in electronic and system-level manufacturing.
- Analyze production quality metrics and support inspections.
- Investigate and resolve product issues, implementing corrective actions.
- Validate processes and review manufacturing documents.
- Manage supplier quality and participate in audits.
- Ensure compliance with industry standards and support audits.
- Drive improvements to enhance product quality and reduce defects.
Key Skills and Requirements:
- Degree in Engineering, Quality, or a related field.
- Knowledge of industry standards like ISO 13485 and FDA regulations.
- Experience in process validation and handling product issues.
- Ability to understand technical drawings and documentation.
- Strong communication skills and attention to detail.
For more information, please contact Billy O'Brien.
If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists visit the 'Contact Us' page.
Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.
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