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Lead Qualified Person

WALKER COLE INTERNATIONAL LTD
Posted 12 days ago, valid for 10 days
Location

London, Greater London EC1R 0WX

Salary

£55,000 - £66,000 per annum

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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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  • Walker Cole International is seeking a Lead Qualified Person (QP) for a pharmaceutical manufacturer in England.
  • The role involves ensuring GMP compliance, batch certification, and overseeing non-conformances.
  • Candidates should have extensive experience in Quality Assurance within the pharmaceutical industry, preferably with on-site manufacturing experience.
  • The position requires qualifications to be a named QP as per EU Directive 2001/83/EC and effective communication skills.
  • The salary for this role is competitive and commensurate with experience, with a minimum requirement of several years in relevant positions.

Walker Cole International is searching for a Lead Qualified Person (QP) to join a leading Pharmaceutical manufacturer in England. As the Lead Qualified Person, you will ensure GMP compliance for the site and focus on the release of small molecule batches.

Your responsibilities as the Qualified Person will be:

  • The batch certification and release for licensed products manufactured on site and through third party CMOs.
  • To oversee and verify non-conformances and OOS/OOTs in accordance with internal procedures.
  • To lead on manufacturing floor GEMBA walks.
  • To provide support, guidance and advice on Quality matters to all departments within the company, contributing to the company GMP strategy.

The successful candidate for the Qualified Person position will demonstrate the following:

  • Extensive experience in Quality Assurance roles within the Pharmaceutical industry, with on-site manufacturing experience preferred.
  • The qualifications and experience required to be a named QP on the license as defined in EU Directive 2001/83/EC and the Human Medicines Regulations.
  • Effective communication skills to allow collaboration and engagement with all stakeholders across the business.
  • A willingness to be agile and flexible to enable them to adapt to situations when required.

Quality Assurance | QA | QP | Qualified Person | Deviations | OOS | OOT | GEMBA | GMP | Good Manufacturing Practice | Orange Guide | Small molecule

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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.