Quality Assurance Specialist
other jobs taylorollinson Ltd
Added before 3 Days
- England,East of England,Cambridgeshire
- full-time
- £32,000 - £40,000 per annum
Job Description:
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.
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.
Job number 1683400
metapel
Company Details:
taylorollinson Ltd
Taylorollinson Ltd is an independent, specialist recruitment organisation with offices on Manchester Science Park and Milton Park, Oxfordshire. We hav...