OGT, Cambridge, UK +1
We are looking for a proactive and detail-oriented Quality Assurance Associate to join our Cambridge-based Quality function within a regulated medical device manufacturing environment operating to ISO 13485, MDSAP, EU IVDR and FDA requirements.
You will combine strong technical and analytical thinking with excellent interpersonal skills. You will need to be comfortable working with controlled processes, procedures, records and data, with the attention to detail and critical thinking necessary to identify inconsistencies, investigate issues and ensure that quality principles are applied.
The role requires an individual who can build positive relationships with colleagues across Quality, Manufacturing, Operations, R&D and other functions. You should be able to explain quality requirements clearly, listen to different perspectives and challenge constructively.
You'll need to be organised and resilient, comfortable juggling multiple priorities and able to take ownership of actions through to completion.
Application is via CV and a one-page covering letter outlining your suitability for the role, salary expectations and notice period.
Please note that we will need to establish your right to work during the recruitment process.
OGT is a leading global provider of clinical and diagnostic genomic solutions. We believe in creating products and partnerships that enable clinicians to deliver personalised healthcare to patients and that empower clinical researchers to develop the next generation of precision medicines.
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