Job Description

A reputable and well-established Medical Device company is actively recruiting a Document Control Specialist for their team in Oxford.

Please note that you must meet all the criteria set out below for your application to be considered. Suitable candidates will be contacted within 5 working days. If you are not contacted by us within that time, please consider your application unsuccessful on this occasion.

The main responsibilities will include but not limited to:

• Manage and maintain all controlled company documents.
• Implement and manage document hierarchy and process systems.
• Verify document quality and accuracy.
• Coordinate activities related to the document control procedure.
• Train employees on document control procedures and use of controlled documents.
• Prepare reports and assist with audits to ensure document accuracy and consistency.

To be successful, you will need to meet the following:

• Bachelor's degree in a scientific or technical discipline.
• Minimum 2 – 5 years of relevant experience within the Medical Devices industry in the UK.
• Experience in an FDA regulated environment.
• Knowledge of industry standards and regulatory requirements.
• Strong organizational, attention to detail and multitasking skills.
• Proficiency in Microsoft Office and quality management systems.
• Applicants should be available for face-to-face interviews in the location mentioned above. 

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Hiring? If you need help filling a similar position in your company, please contact us on +44 (0)208 137 0401 or click here.

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