The Role
Specialist, QA Systems will join the Document Control Team and, along with other team members, will act as a key point of contact and provide cross-departmental support for a variety of document management systems and processes.
Note this is an on-site role.
Key Duties and Responsibilities:
* Preparation and issuance of controlled documentation to support manufacturing and testing activities
* Development and maintenance of the Documentation Management System
* Provision of training and user support for the Document Management System
* Management of the Document Archive and Record Retention Systems
* Maintenance of other document systems and processes e.g. SharePoint, Periodic Review tracking.
* Delivery of GMP/GDP training
* Participation in the internal and external audit program
* Collection of quality metric data
* Support completion of investigation/CAPA activities as applicable to role
* Interface with relevant departments to ensure compliance with corporate policies, GMP and regulatory requirements
* Authoring, review and approval of QA-related procedures
Qualifications, Knowledge and Skills Required:
* The successful candidate will hold a BSc in life sciences/pharmacy or similar
* A minimum 1-2 years' Quality experience in a pharmaceutical environment is adventitious
* Working knowledge of cGMP requirements for manufacturing and/or systems and compliance.
* The candidate must be able to work across a team matrix in order to meet accelerated timelines
* The candidate must be able to reprioritise tasks as required to meet changing demands.
The Next Step for you:
Should this position be of interest to you please submit your CV to Jessica from Next Generation Recruitment using the apply button.
Next Generation will never share your data outside of our organisation without your prior written consent.
Please read our Data Protection Policy on our website.
If you require any reasonable accommodations during the recruitment process please let us know and we will do our best to support you.
