Quality Assurance Specialist

Salary: £33,600 – £42,000 per year

Quality Compliance Specialist – Hertfordshire

Opportunity:

Are you currently working in quality assurance looking for your next job opportunity? Have you implemented or maintained quality systems? Do you have good experience in GMP and GDP? Want to work for a growing pharmaceutical company? If yes then please read on.

Your role as a Quality Compliance Specialist based in Hertfordshire will involve:

* Maintaining the company’s Quality Management System.

* Monitoring the performance against quality compliance objectives.

* Maintaining schedule of routine GMP and GDP compliance activities.

* Maintaining schedule of routine non-GMP and GDP compliance activities (e.g, Home Office licencing).

* Creating and maintaining assigned SOPs.

* Monitoring ongoing product supply standards against registered and specified details.

* Identifying compliance gaps and making recommendations for continuous improvement.

* Supporting product recalls and stock recoveries.

* Administering product technical complaints, including progressing their investigation and report.

* Implementing product and process change controls.

* Implementing deviation investigations and CAPA’s.

* Compiling periodic product quality review reports in conjunction with contract manufacturers.

* Compiling data for reports and presentations.

* Maintaining currency of European GMP and GDP requirements.

* Implementing changes that arise from either the introduction of new or revised GMP and GDP regulations.

This is a full time permanent job based working at the site in Hertfordshire. It is a site based office role. The salary is around £33,600 – £42,000per annum negotiable for the right candidate.

Skills:

To apply for the role of Quality Compliance Specialist you will have the following:

* A degree level qualification, ideally in the life sciences.

* A minimum of 2 years recent experience working in this quality compliance role.

* Ideally working knowledge of oral and parenteral dose-form manufacture and testing.

* An awareness of European GMP and GDP legislation.

* Proven organisational and project management skills.

* IT skills, particularly in relation to using databases and familiarity with commercial software.

How to Apply:

To apply for this one off opportunity, please send a word copy of your CV to me now by clicking on the Apply button or call me for a confidential chat. Please ensure you have read and agree to our Privacy Policy on our website.

If this sounds like the role for you or a colleague then please don’t hesitate to contact us. If we manage to successfully fill a permanent placement from your recommendation then we will send you a cheque of £300. We also have many incentive schemes for referring contractors/temp staff so please contact us with the referral and we can provide you with more information.

For a list of our current vacancies, please apply.

If you do not hear from Quality Start within 2 weeks your CV has not been short listed for this role.

Quality Start are acting as a specialist recruitment consultancy for this role.