Description
Position Summary:The successful candidate will have a strong background in Quality Management Systems.
This position is responsible for carrying out tasks and projects related to management of Quality Assurance activities as required by Good Manufacturing Practice (GMP).
These activities include change control, investigation, supplier qualification, incoming materials release, batch release, annual product review and validation compliance activities.
Main duties and responsibilities:
Providing support and direction to all departments in respect of specific quality system elements to ensure business, quality and compliance goals are met.
To carry out tasks related to the administration of site nonconformance management systems including review and/or approval of investigation.
Qualifications and Experience:
ESSENTIAL:
Bachelors Degree in a scientific/technical discipline required.
A minimum of 2 years' experience in a quality, manufacturing, validation or compliance role within the biological and/or pharmaceutical industry.
Knowledgeable of FDA/EMEA regulatory requirements applicable to biologics and/or pharmaceuticals.
Ability to apply GMP regulations and other FDA and international guidelines to all aspects of the position.
To learn more about this excellent opportunity to join a renowned Pharmaceutical company please contact Sarah Irvine on .