My client is an emerging cancer immunotherapy company developing cell-based treatments for cancer and severe viral infections. The company have a clear vision to make CAR-T a mainstream therapy for eradicating cancer. They are developing safer, cheaper, consistent and durable CAR-T drugs for haematological and solid tumours.
Due to continuous growth in the company, my client is now looking for a driven, organised and proactive individual to join their team as a QA Supervisor.
You will become an integral part of the Quality team, supervising operations on site, ensuring everything is conducted according to all internal and external quality and regulatory compliance requirements and will additionally be responsible for overseeing correction and remediation activities affecting the quality system such as data quality issues, oversight of root cause analysis, and developing QA procedures.
What do you need?
A minimum of 5 years working experience within a QA role in a GMP regulated Life Science company, and previous Supervisory experience in a similar role is essential.
It’s fast-paced collaborative environment, so you need to be a clear communicator, to be able to work well under pressure while always thriving for excellence, and bringing new innovative idea’s forward for processes improvement.
If you’re an ambitious, QA leader looking to develop your expertise further, and want to become an integral member of an award-winning Biotech then get in touch ASAP.
***This client is still actively interview, onboarding remotely, and they offer relocation assistance if needed- You even get an extra day off in your first two weeks to help with settling in if you’ve relocated!***"
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