Senior Quality Systems Officer

  • Location:

    Wrexham, Wales

  • Sector:


  • Job type:


  • Salary:

    £35000.00 - £40000.00 per annum

  • Contact:

    Alannah Fisher

  • Contact email:

  • Job ref:


  • Published:

    6 months ago

  • Expiry date:


  • Start date:


Senior Quality Systems Officer
Salary up to £40K per annum

Do you have experience of managing Quality Systems within a pharmaceutical environment?
Are you an expert in cGMP, GDP or other industry best practices? Do you have an excellent eye for detail?
A fantastic opportunity has arisen for a Senior Quality Systems Officer to join my client's Quality Systems team!

As a Senior Quality Systems Officer you will be responsible for maintaining and improving site quality systems in line with company, corporate and international standards to support cGMP/GDP compliance and to meet business expectations.

Responsibilities of the Senior Quality Systems Officer will include:

* Leading the continuous improvement of site quality systems, including Technical Agreements, Annual Product Reviews, Planned Change, Deviations, CAPA, Complaints and Internal Auditing
* Monitoring the effectiveness and level of site wide compliance, application of risk management, focussed initiatives and delivery of training, whilst maintaining associated GMP operating procedures and documentation.
* Preparation of Technical Agreements and Annual Product Reviews
* Liaising with Clients and vendors to ensure all documentation is completed as defined by cGMP/GDP.
* Support other site projects, from a Quality Assurance perspective, by reviewing and approving where appropriate, project documentation including risk assessments, ensuring compliance with cGMP/GDP, company and other regulatory agency requirements.

The ideal candidate for the Senior Quality Systems Officer role will have:

* a BSc (or equivalent) in a scientific discipline
* substantial experience within the pharmaceutical or equivalent quality assurance environment, ideally with experience of liaising with clients in relation to application and generation of technical contracts or agreements.
* a thorough understanding of cGMP/GDP and its relationship with Technical Agreements and Annual Product Quality Reviews and other current best practices for the Pharmaceutical Quality System, and also the ability to work with concepts and practices often outside the original area of academic qualification.

If this sounds like you then please apply now!

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