Validation Specialist

**THIS IS A HYBRID ROLE AND REQUIRES SITE WORK IN OXFORD - PLEASE DO NOT APPLY IF YOU DO NOT HAVE RIGHTS TO WORK IN THE UK**
We are currently looking for a "CSV Specialist for qPCR Systems" to join a leading biotech company based in the Oxford area. As the CSV Specialist for qPCR Systems, you will be responsible for ensuring the successful introduction and validation of qPCR systems within the company's laboratory environment.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the CSV Specialist for qPCR Systems will be varied; however, the key duties and responsibilities are as follows:
1. Develop and execute validation protocols for qPCR systems.
2. Ensure compliance with regulatory requirements and industry standards.
3. Collaborate with cross-functional teams to support system implementation.
4. Provide training and support to laboratory staff on qPCR system usage.
ROLE REQUIREMENTS:
To be successful in your application to this exciting role as the CSV Specialist for qPCR Systems, we are looking to identify the following on your profile and past history:
1. Relevant degree in a scientific or engineering discipline.
2. Proven industry experience in computer system validation (CSV).
3. A working knowledge and practical experience with qPCR systems.