Your role will be to ensure continued compliance with all relevant regulatory and quality requirements. You will need to provide timely identification of any regulatory changes to ensure the business is up to date and that no negative impacts occur. You will be handling various technical documentation such as DMR, recall files where necessary and product registration documents. You will be involved in the product registration process & CE Marking.
As well as a dynamic role they offer a phenomenal work environment at their state of the art facility with manufacturing on-site and outstanding facilities including a subsidised canteen.
To apply for this role you should demonstrate the following skills/experience:
- A good understanding of Medical Device Regulations
- Previous experience in a similar RA or QA/RA role
- Previous experience in a manufacturing environment is preferred
We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.