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QA Specialist

Smart4Sciences
Posted 12 hours ago, valid for 7 days
Location

Salford, Greater Manchester M6 5BR

Contract type

Full Time

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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  • An exciting opportunity for a QA Specialist has arisen in a growing pharmaceutical company located in the Salford area of Manchester.
  • The ideal candidate should have 1 to 2 years of experience in quality assurance within the pharmaceutical sector.
  • Key responsibilities include overseeing product quality, ensuring compliance with GMP and GDP standards, and providing administrative support.
  • The position offers a competitive salary, along with benefits such as a generous pension plan, free car parking, and holiday entitlement.
  • This role presents a great chance for career progression in a dynamic environment.

Role: QA Specialist

Location: Manchester (Salford area)

An exciting opportunity has become available for a QA Specialist to join a growing pharmaceutical company that specialise in parallel import. The position will be based in the Salford area of Manchester. This would be a great opportunity for an experienced quality professional with one or two years of experience to join a growing team to accelerate progression within their career

Job Description, QA Specialist

  • Responsible for Database control within the department
  • Administrative support to Customers and Colleagues
  • Error Recording, execution of CAPAs and QMS compliance
  • Oversee the quality of all manufactured products and ensure adherence to GMP, GDP and documented procedures.

Responsibilities of the QA Specialist

  • Promote compliance with GMP and company policies
  • Reviewing Batch Record and GMP release
  • Provide support to ongoing preparation for Regulation License Approval
  • Develop and Enhance the QMS activities involved with the release of the product
  • Documentation writing including reports, non-compliances and deviations

Experience

  • Scientific degree or equivalent
  • Product release experience
  • 2 years' experience working within pharma QA
  • Experience of working within a compliance team working on procedures and policies
  • Hands on approach and a can do attitude

Benefits

  • Great Career progression
  • Generous company pension
  • Free car parking
  • Holiday entitlement
  • Annual pay review

To apply for the Senior Quality Control Analyst or here more information, please contact Jack Challinor at Smart4Sciecnes on

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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.