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Quality Assurance Specialist

taylorollinson Ltd
Posted a day ago, valid for 17 days
Location

Cambridge, Cambridgeshire CB2 8AG, England

Salary

£28,000 - £33,600 per annum

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Contract type

Full Time

Health Insurance

In order to submit this application, a Reed account will be created for you. As such, in addition to applying for this job, you will be signed up to all Reed’s services as part of the process. By submitting this application, you agree to Reed’s Terms and Conditions and acknowledge that your personal data will be transferred to Reed and processed by them in accordance with their Privacy Policy.

Sonic Summary

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  • The Quality Assurance Specialist position is located in Cambridge within the biotechnology sector.
  • The salary for this full-time, permanent role ranges from £32,000 to £40,000, depending on interview performance and experience.
  • Candidates must have multiple years of experience working within a cGMP-compliant Quality Management System (QMS).
  • The role involves leading the implementation and management of a cGMP-compliant QMS and ensuring procedural compliance across the business.
  • Applicants must have current UK work eligibility and relevant industry experience in biotech, DNA, or pharma settings.

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.

Apply now in a few quick clicks

In order to submit this application, a Reed account will be created for you. As such, in addition to applying for this job, you will be signed up to all Reed’s services as part of the process. By submitting this application, you agree to Reed’s Terms and Conditions and acknowledge that your personal data will be transferred to Reed and processed by them in accordance with their Privacy Policy.