Our client, a major pharmaceutical company located in County Durham, has a number of long term temporary vacancies for Quality Assurance Officers with relevant experience in product release and cGMP compliance. Some but not all of these Quality Assurance Officer positions may involve shift working, for which there is a generous shift allowance.
As a Quality Assurance Officer you will have the following responsibilities:
- You will ensure that all products released for sale or further processing comply with cGMP standards, product quality specifications and regulatory requirements.
- You will also generate and review product related technical documents, and collate and interpret data such as analytical results/trends and regulatory, validation and engineering information.
- To lead and direct investigative work into products failing to meet requisite standards (and regulatory issues).
- You will also lead investigative work and develop and agree corrective actions.
Our client is looking for individuals with a strong background in Quality Assurance, good knowledge of cGMP and regulatory requirements and the ability to manage multiple activities concurrently within high volume, complex areas. Excellent communications skills are also required, together with demonstrable leadership and decision-making abilities.
For more information, or to apply for these Quality Assurance Officer roles, please contact Graeme at CK Science on 0191 384 8905 or email firstname.lastname@example.org. Please quote reference DH20139 in all correspondence.