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Quality Officer

Job Title: Quality Officer
Contract Type: Permanent
Location: South Wales
Salary: £20k-£25k
Contact Name: Matthew Rollinson
Contact Email:
Job Published: November 27, 2020 14:32

Job Description

Quality Officer




Permanent role




£20,000 - £25,000


We are working with a Pharmaceutical company in South Wales, they provide services in drug development, clinical trials and commercial packaging. This allows for quicker product development to market studies, approval and patients. They are seeking a Quality Officer to work in Operations.


What you’ll do:


To assist the Quality Management team in ensuring that all activities are in compliance with current Good Manufacturing Practice (GMP) standards in accordance with company policies to meet business requirements.


  • To work with primarily, the Manufacturing and Packaging departments to provide Quality Assurance (QA) guidance and expertise in the resolution of quality issues.
  • To ensure the timely release of product by the review of the critical process parameters of the batch documentation to assess the quality, safety and efficacy of the products prior to Qualified Person certification, in accordance with agreed schedules and Service Level agreements.
  • To perform process and departmental audits against the relevant GMP standards to ensure continued compliance and improvement of systems and processes.
  • The job holder is responsible for the interpretation of GMPs for all manufacturing and packaging areas, including development and distribution stages with support from the Head of Quality and Site QP’s
  • The scope of the Quality Officer role covers all manufacturing and packaging areas across site*.(*subject to entry and working practices and related SOPs)


Your background:


The job holder will ideally have experience and knowledge within the pharmaceutical industry, with a diverse knowledge of various dosage forms in both manufacturing and packaging.


  • Previous experience within a Quality department is also essential, ideally within a cGMP/pharma environment.
  • Excellent written and verbal communication skills are required by the job holder as in the course of the duties. The job holder will need to communicate with personnel outside of the Quality group, with external clients, in order to ensure timely completion of business demands and customer service.
  • The job holder will need to be able to lead by example and get results through persuasion and co-operation.


On this occasion, LiCa Scientific is working as an employment agency.



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