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QA Specialist

RBW Consulting
Posted 15 hours ago, valid for a month
Location

Barking, Greater London IG11 8DB

Salary

£32,000 - £38,400 per annum

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Contract type

Full Time

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Sonic Summary

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  • The Quality Assurance Specialist position is available in a growing service and solutions provider in the pharmaceutical industry based in Greater East London.
  • Candidates should have experience within the pharmaceutical industry, particularly with GMP and regulatory audits, and a degree or relevant industry experience is required.
  • The role involves providing technical quality support, reviewing analytical methods, and conducting audits to ensure compliance with GMP guidelines.
  • The company is expanding due to recent project wins, and the position promises immediate impact and value in a fast-paced environment.
  • The salary for this position is competitive, and applicants should have at least several years of experience in a regulated environment.

Quality Assurance Specialist

Are you passionate about ensuring top-notch quality in the pharmaceutical industry? Would you like somewhere where your impact is immediate and valued?

We are now starting to shortlist for an incoming, key hire for a growing service and solutions provider within the chemistry space, based in Greater East London. Given the businesses recent success in winning a number of new projects, they are now going through an expansion project.

For this role you will take on a wide range of technical quality responsibilities that relate to the analytical services team. Some of the key responsibilities will include:

  • Provide technical quality support for new and ongoing projects.
  • Review and approve analytical methods, test data, equipment maintenance, and more.
  • Support investigations and ensure compliance with GMP and regulatory guidelines.
  • Conduct self-inspection audits and assist in external inspections.
  • Promote quality improvements and prevent re-occurrence of non-compliance.

Key experience:

  • Educated to degree level or with relevant industry experience
  • Experience within the pharmaceutical industry
  • GMP experience is essential
  • Experienced in regulatory audits and working in a regulated environment.
  • A team player, with the ability to work in a growing and fast paced set up

For further information please contact Mark Bux-Ryan.

Quality, QA, system, operations, analytical, audit, capa, investigation, deviation, analytical, reports, validation, documentation, officer, specialist, executive, GMP, manufacturing

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