Quality Assurance Specialist
Location – Cambridge
Sector – Biotechnology
Salary – £32,000 - £40,000 (depending on interview performance & experience)
Full time, permanent role
Do you have experience working within a cGMP-compliant Quality Management System (QMS)? Do you have prior experience leading the implementation of a new QMS within a biotech or pharma setting?
We have an exciting opportunity available with a biotechnology company in Cambridge. Our client is looking to onboard an experienced QA professional with prior experience leading QMS activities.
Applicants must have current UK work eligibility.
The Role
As a Quality Assurance Specialist, you will be responsible for:
* Leading the implementation and management of a cGMP-compliant QMS,
* Ensuring procedural compliance throughout all parts of the business,
* Leading QMS activities to ensure the successful manufacturing of synthetic DNA products.
Skills and Experience Needed
The ideal candidate will have the following:
* Multiple years of experience working within a cGMP-compliant QMS (essential).
* Hands-on experience leading QMS activities within a cGMP environment – e.g. CAPAs, deviations, change controls, internal & external audits, documentation management (essential).
* Prior experience implementing and managing a cGMP-compliant QMS (essential).
* Comfortable working within both a paper and electronic QMS (eQMS) (essential).
* Relevant industry experience within a biotech / DNA / pharma setting (essential).
* Existing UK work eligibility (essential).
The Package
As an up-and-coming Cambridge Biotech, our client can offer a competitive salary and benefits package including private pension and private health insurance.
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