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Quality Assurance Manager

JR United Kingdom

Sheffield

On-site

GBP 40,000 - 60,000

Full time

2 days ago
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Job summary

An innovative pharmaceutical company based in Sheffield is looking for a Quality Assurance Manager for a 12-month contract. The ideal candidate will ensure compliance with quality legislation, lead external audits, and manage GMP/GDP documentation, contributing to the company's supply chain operations. This role offers a competitive salary and benefits, with a focus on quality management in the pharmaceutical industry.

Qualifications

  • Extensive quality experience in the pharmaceutical industry.
  • Previous experience of acting or deputising as a Responsible Person.
  • Experience working with medical devices or medicinal products.

Responsibilities

  • Acts as 'Responsible Person' or deputises when required.
  • Leads external supplier audits and qualification.
  • Requests, reviews, and processes GMP/GDP documentation.

Skills

Quality Assurance
GMP/GDP Documentation
Supplier Audits

Education

Life Sciences Degree

Job description

Social network you want to login/join with:

Quality Assurance Manager, Sheffield, South Yorkshire

Client:

Pharma-Partners Recruitment Limited

Location:

Sheffield, South Yorkshire, United Kingdom

Job Category:

Other

EU work permit required:

Yes

Job Views:

1

Posted:

04.06.2025

Expiry Date:

19.07.2025

Job Description:

Job title: QA Manager (12 month contract)

An innovative pharmaceutical company in Sheffield is seeking a QA Manager to join their growing team. This role will be responsible for ensuring the company's supply chain operations comply with all relevant quality legislation.

Responsibilities:

  • Acts as 'Responsible Person' or deputises for the 'Responsible Person' when required.
  • Acts as or deputises for the Management Representative relating to the development and continuous improvement of the processes needed for the Quality Management System.
  • Leads external supplier audits and qualification.
  • Requests, reviews, and processes all GMP/GDP documentation as defined in the QTAs.

Requirements:

  • Extensive quality experience in the pharmaceutical industry.
  • Previous experience of acting or deputising as a Responsible Person.
  • Experience working with medical devices or medicinal products.
  • A life sciences degree would be beneficial.

Salary and benefits:

A highly competitive salary and wider benefits scheme is on offer.

To apply for this position or hear further details, please contact Freddie Hill via [emailprotected].

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