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.
I'm interested in this job
Please use the form provided to get in touch with us and we will respond as soon as possible.
Compulsory fields are in bold.
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