A new instruction for a Regulatory Affairs Associate with a global manufacturing client and key employer.

Duration
The role is initially being offered on a medium fixed term basis for 12 months. Thereafter to be confirmed.
A good rate of pay is available for a support role of this level.

What does the role entail?
You will complete day to day departmental administrative activities.
Carry out duties in line with regulatory affairs and ensure compliance with regulatory legislation and guidelines a company processes and procedures.
The Regulatory Affairs Associate will provide regulatory/technical support to the Senior Regulatory Affairs Specialist and be part of the Global Regulatory Affairs Team.
You will complete day-to-day departmental administrative duties.
Create and maintain Regulatory Technical documentation based on provided templates and guidance from the Senior Regulatory Affairs Specialist.
Understand upcoming UK MDR and essential standards to the products (Regulatory intelligence will be provided)
MD artwork approval. Training will be provided based on applicable standards.

The experience we are seeking:
The Regulatory Affairs Associate position is considered ideal for someone who already has a couple of years’ experience within the medical device industry, with any experience gained within the QA sector, also ideal.
You will require a proven ability to resolve issues
A team player.
Great communication skills.

If you would like to be considered for the above then please forward your CV providing an approximate salary banding you are seeking, for a support level position of this nature.





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