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Quality Manager

JR United Kingdom

Watford

On-site

GBP 40,000 - 60,000

Full time

24 days ago

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Job summary

A leading pharmaceutical company in Watford is seeking an experienced QA Manager for a 12-month contract to ensure compliance with quality legislation within the supply chain. This role requires extensive experience in the pharmaceutical industry, including acting as a Responsible Person and working with medical devices. Competitive salary and benefits are offered to attract top talent.

Qualifications

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

Responsibilities

  • Responsible for ensuring supply chain operations comply with quality legislation.
  • Acts as 'Responsible Person' or deputises for it when required.
  • Leads external supplier audits and qualification.

Skills

Quality experience in the pharmaceutical industry
Responsible Person
Experience with medical devices

Education

Life sciences degree

Job description

Social network you want to login/join with:

Quality Assurance Manager, Watford, Hertfordshire

Client:

Pharma-Partners Recruitment Limited

Location:

Watford, Hertfordshire, 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 London 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 audit 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 are on offer.

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

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