Do you have a background in Quality Assurance Document Management ? If so, we’d love to hear from you! Valneva is an award-winning, speciality vaccine company providing prevention against diseases with major unmet medical needs, and we are currently hiring for a QA Specialists within Document Management to join us during this unprecedented time of growth.
Job Summary
Responsible for document control and document archive. Assist in maintaining a comprehensive quality management system to achieve inspection readiness all portfolio products
Responsibilities
- Maintain a system of document control to meet the requirements of the company, taking into account any regulatory requirements i.e. GDP I cGMP I FDA
- Maintain company archive and pre archive system to ensure adequate and secure protection of quality documentation and data.
- Manage databases within the Quality System
- Good Manufacturing Practice for the manufacture and testing of pharmaceuticals
- Provide support during audits of Valneva Scotland Ltd
- Support and take part in Continuous Improvement activities
- Provide support for Pilgrim electronic document management system where required
- Perform training in areas of expertise where required
- Work within the Global Quality team to ensure efficient and effective roll-out of Global Quality Documents
- Support Quality Assurance activities as directed by line manager or Head of Quality Assurance
- Provide administrative support for Quality Assurance activities as directed by line manager or Head of Quality Assurance
- To undertake any other duties as requested by the line manager in accordance with company requirements
Job Requirements
Experience:
- Relevant experience in business administration/ document control and archiving
- Experience of GMP environment and specifically Quality Operations/ Quality Assurance
Required Skills:
- Self-motivated and conscientious team player
- Effective communication skills
- Excellent organisational skills