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Quality Officer, Pharmaceutical company

Vacancy Title: Quality Officer, Pharmaceutical company
Contract Type: Permanent
Location: Bolton, Greater Manchester
Industry:
Salary: £27500 - £32000 per annum
REF: J910952_1636558138
Contact Name: Tom Hammond
Contact Email: tom.hammond@russell-taylor.co.uk
Vacancy Published: 25 days ago

Vacancy Description

Quality Officer, Pharmaceutical company

Location: Bolton

Type: Permanent

Salary: £27,500 - £32,500 DOE

Hours: Rotating, Week 1 (Mon - Thurs) 6:00- 14:00. Fri 6:00 - 13:00

Week 2 (Mon - Thurs) 14:00 - 22:30, Fri 13:00 - 17:30

Additional: Parking onsite, company pension etc.

Our Client, a growing Pharmaceutical - manufacturing company are looking to recruit a Quality Officer to assist with the 'shop - floor' QA activities and preservation of the QMS. This could be an ideal role for someone with some basic Pharmaceutical QA experience or someone working in an QC hybrid position (with some CAPA, OOs, OOt etc experience in a GMP capacity).

The Role:

  • Support the QA Operations Manager with operational quality oversight, carrying out duties as directed to ensure that the required GMP standards and quality standards are met
  • Providing Quality oversight and technical input across all aspects of product manufacturing
  • Support production investigations such as Deviations and OOS
  • Support change control and CAPA activities
  • Prepare and review quality documentation including SOPs, technical documents
  • Provide strong factory floor presence, contributing to "Quality on the floor" including coaching, mentoring and training of operational teams on GMP and technical aspects of production
  • Support effective problem solving, co-ordinating with quality and operational functions to devise and implement effective solutions
  • Identify opportunities for continuous improvement and support the QA Operations Manager in delivering continuous improvement objectives
  • Support self-inspections and support regulatory inspections

The Person:

  • Will hold a Degree in a relevant/ Scientific discipline.
  • Experience in CAPA activities in an GMP setting (substantial amount of experience).
  • Experience updating / writing SOPs.
  • The ideal candidate will come from solid dose - pharmaceutical industries but not essential.

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