Job: Regulatory Affairs Specialist

Job Title: Regulatory Affairs Specialist
Contract Type: Contract
Location: Essex
Salary: Competitive salary in line with experience
Start Date: 2018-08-09
Job Published: 5 days ago

Job Description

This new position for a Regulatory Affairs Specialist comes from a global leader in the development of medical devices. They are seeking an experienced regulatory professional with knowledge of medical device regulations to support current activity for a 12 month contract period.

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
To apply for this position apply online or call Tanya Zero on 01212373340. This role is a 12-month contract position and is urgent so please get in touch!
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.