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Quality Specialist

CK Group- Science, Clinical and Technical
Posted 2 days ago, valid for 8 days
Location

London, Greater London SW1A2DX, England

Salary

£0 - £267 per day

Contract type

Full Time

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Sonic Summary

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  • CK Group is seeking a Quality Specialist for a 12-month contract in the pharmaceutical industry, with the flexibility to work fully remotely or from their London site.
  • The position offers a salary of £331.27 per day and requires knowledge of quality systems principles and practical application, along with experience in cGMP.
  • Candidates should possess excellent organizational skills, effective time management, and the ability to manage multiple tasks independently.
  • The role involves managing project quality activities, conducting compliance and quality gap analysis, and delivering a Quality Agreement plan with stakeholders.
  • Applicants must have the right to work in the UK and may be subject to a basic Disclosure and Barring Service (DBS) check.
CK Group are recruiting for a Quality Specialist, to join a company in the pharmaceutical industry. This is based at our clients site in London, but can be worked fully remotely. This role ison a contract basis of 12 months.


Salary:

PAYE 331.27 per day.


Quality Specialist Role:
  • Management of project Quality workstream activities according to the project plans.
  • Contribute to compliance and quality gap analysis.
  • Deliver Quality Agreement plan between appropriate internal and external stakeholders and signatories.
  • Negotiation of Quality Agreement Content to deliver plan.
  • Monitor effective and timely registration through flow of information from sites and between project function.

Your Background:
  • Knowledge of quality systems principles and practical application.
  • Knowledge and experience applying cGMP.
  • Excellent organizational skills, effective time management, ability to clearly identify priorities and manage multiple tasks.
  • Demonstrated ability to work and collaborate in a matrix organization, across multiple and geographic boundaries and work independently with minimal supervision.
  • Technical knowledge of manufacturing, quality change and regulatory activities related to pharmaceutical products.

Company:

Our client is one of the largest global healthcare companies researching, developing and supplying innovative medicines, vaccines and healthcare products with their global headquarters in the UK. They invest around 1bn in research and development in the UK annually.


Location:

This role is based at our clients site in London. However, can be worked remotely.


Apply:

It is essential that applicants hold entitlement to work in the UK. Please quote job reference (Apply online only) in all correspondence.


Please note:

This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.


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By applying, a CV-Library account will be created for you. CV-Library's Terms & Conditions and Privacy Policy will apply.