Job Description
Newbury
An opportunity has arisen for a QA Associate to work within my clients QA group at their facility in Berkshire.
The Successful candidate's main duties will be:
·Ensure that the client's vaccine is manufactured in accordance within the principles of Good Manufacturing Practice.
·Assist in the maintenance and continual improvement of the quality management system and the development of strategies to ensure that product quality and customer satisfaction are maintained.
·Continuous quality improvement of products, processes and services.
·Documentation review and release including batch records, change controls, validation documents, product literature and standard operating procedures.
·Conduct internal process audits and QA training initiatives. Maintain QA metrics and act as an adviser on best Quality practice.
You must have a biological science degree and/or a relevant professional qualification and microbiological experience in bacteriology or virology.
Hands on experience in the Quality Department of a Pharmaceutical or Biotechnology company is essential as is experience of documentation and process auditing and CAPA programmes.
Due to the location your own transport will be essential as there is limited public transport.
If you feel that you have the right experience for this position then please apply with an updated CV or contact Harrison Smith on 01442 898 916 or harrison.s.a4ljeb7g6gj@entechts.aptrack.co.uk