Quality Assurance Officer

This Listing has Expired

We are sorry to say that this job is no longer available. However we are experts in recruitment and we are sure we can help you.  You can view the related jobs on this page and if there is nothing suitable then please contact us on 0114 238 0012, register your CV, or register for job alerts all in confidence.

  • A leader in the manufacture of a whole host of pharmaceutical products across Primary and Secondary Care
  • An expanding business with a strong national presence, looking to go international in the long term
  • New facilities, with excellent investment for the future

Are you a Quality Control or Quality Assurance (QA QC) professional working in Pharmaceutical manufacturing? Our client – a leader in pharmaceutical production across Primary and Secondary care – is looking for a Quality Assurance Officer to ensure the efficient running of the day to day quality function and take a lead in responding to QA queries.

 

Your experience:

 

Required:

  • Scientific / Life Sciences Degree (preferably Pharmacy / Pharmaceutical Sciences)
  • 2-5 years’ experience in Pharmaceutical Quality Assurance
  • Ability to write and review QA documentation, including SOPs, validation protocols, GMP Deviations, Change Controls, CAPAs, Technical Agreements, Risk Assessments, audit reports and the handling of recalls.
  • Exposure and understanding of regulatory requirements of bodies such as the MHRA
  • Understanding of formulation development and laboratory GMP, GCP / GxP requirements
  • Background in the handling quality queries
  • Commercially aware, with the ability to manage cross-functional interests
  • An understanding of needs within a small business environment, and a tight knit team

 

Highly desirable:

  • Experience in working with Specials and IMPs

 

Your new job:

 

  • Work as a key component of the quality team in a highly regarded manufacturer undergoing expansion
  • Write and review QA documentation, including SOPs, validation protocols, GMP Deviations, Change Controls, CAPAs, Technical Agreements, Risk Assessments, audit reports and the handling of recalls.
  • Act as the Quality lead for continuous improvement initiatives
  • Update and liaise with managers regarding Quality of manufacture
  • Mentor and develop more junior members of staff as to Good Clinical and Good Manufacturing Practices
  • Maintain the QC function according to company SOPs
  • Support the generation of regular data metrics

 

Your new partner company:

  • A leader in the manufacture of a whole host of pharmaceutical products across Primary and Secondary Care.
  • An expanding business with a strong national presence, looking to go international in the long term
  • An IMP licence holder, with a view to capitalise on the Clinical market and develop business further.

 

The package:

 

Our client recognises the need to get the right person in the role. As such, they have agreed to be flexible and negotiable as to salary. A consultant with Zest would however be happy to give you more information in a preliminary conversation.

 

Zest is working to a tight deadline for this position, so please apply now for a CV review, or get in touch with Jason Cox at Zest Medical to learn more.