We have a fantastic new opportunity working a busy Quality Assurance department for a QA Project Support. This role will be responsible for supporting business wide projects across multiple departments.
The successful candidate, will manage to completion the delivery of projects which have significant Quality Assurance and Regulatory impact on requirements.
These projects will have a direct impact on business elements such as compliance, cost saving and process efficiency. You are required to ensure that company wide projects meet all requirements of relevant regulatory standards and Regulations: (ISO13485, FDA 21CFR part 820 and the IVDR).
Working knowledge of FDA part 820, ISO13485, cGMP, IVDR
Experience of working within RA/QA environment within an IVD or medical device company
Working in a Quality Assurance Manager/Manager Level/Supervisor level - to ensure compliance
Knowledge of the application of quality systems in manufacturing.
Knowledge of New Product Development
Excellent communication skills both written and verbal
To have a good understanding of Quality principles/Quality systems and regulations for IVD/medical device company
To be flexible to the need of the business
You must be eligible to work in the UK. Learn more
- Agency: SRG
- Reference: J2157162
- Posted: 6th November 2020
- Expires: 4th December 2020