Description
Responsibilities:To support the management of GMP compliance systems.
To assess compliance systems on ongoing basis and identify opportunities for process improvement.
To develop and improve quality systems by identifying areas for improvement and take corrective action as required to ensure continuous improvement in accordance with Continuous Improvement Process.
Manages entry of nonconformance records into the appropriate electronic system.
Approves closure of nonconformance investigations on completion of the investigation and associated corrective actions.
To carry out tasks related to the management of project and site change control systems.
Qualifications and Experience:
* Bachelors Degree in a scientific/technical discipline required.
* A minimum of 5 years experience in a quality, validation or compliance role within the Medical Device or pharmaceutical industry.
* Knowledgeable of FDA/EMEA regulatory requirements. Ability to apply GMP regulations and other FDA and international guidelines to all aspects of the position.
If you would like to apply for the position please contact Sarah Irvine on . Otherwise submit your upto date CV.