ISO / Compliance Manager

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Job description

Vicon is the world leader in Motion Capture, developing high-performance software and innovative hardware products for the entertainment, engineering, and medical industries. Vicon systems are a crucial tool for measurement and 3D tracking for cutting-edge science including biomechanics, robotics, and virtual or augmented reality. Vicon products have been used in many major feature films, video games, and commercials. We have offices in Yarnton, Denver, Los Angeles, and Auckland.

Vicon Motion Systems Ltd is a subsidiary company of Oxford Metrics Plc.

We are seeking an ISO/Compliance Manager who will be responsible for implementing, maintaining, and delivering quality and compliance within the company as well as liaising with other group companies to achieve common quality and compliance policies.

Responsibilities

The role consists of the following key areas:

• Maintaining the company’s ISO-9001 and ISO-13485 Quality Manuals, procedures and related documentation.

• Understanding of the MDD & MDR regulations.

• Liaison with external companies providing audit assistance.

• Liaison and management of Notified Body audits.

• Management and data provision to provide customers with compliance certification relating to various international requirements such as Li-Po & Li-Ion battery compliance, RoHS, Conflict Minerals, TSA, FDA, CE, Certificates of Origin.

• Liaison with hardware development department regarding compliance issues with products in research and development.

• Liaison with production department to allow for efficient expansion of internal production processes.

• Management of internal records relating to compliance and quality throughout the design/production/manufacturing process.

• Training of staff on quality and compliance issues including health & safety.

• Management of customer audits as well as auditing key suppliers and supplier visits.

Experience

The right candidate will have a technical, manufacturing, or engineering background and will have worked for 5 + years in a quality/compliance role, and be familiar with the various quality-related standards in medical devices both in the UK and the EU. They will likely have experience working with high-tech design and manufacturing.

ISO13485 / MDD/ MDR experience and understanding of medical devices are essential.

For more information please visit our website.

Vicon is an equal opportunities employer.

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