Regulatory Affairs Administrator
- Recruiter
- Confidential
- Location
- Falmouth
- Salary
- 25000.00 - 35000.00 GBP Annual
- Posted
- 07 Sep 2020
- Closes
- 05 Oct 2020
- Sectors
- Admin, Secretarial & PA
- Contract Type
- Permanent
- Hours
- Full Time
A rare and exciting opportunity has arisen for a Regulatory Affairs Associate based in Falmouth on a permanent basis
If you are from a strong administrative, medical devices, regulatory or quality background we would love to hear from you!
Joining a friendly team and reporting to the Regulatory Affairs Executive you will be responsible for:
- Compiling and maintaining the Technical Documentation Files
- Plan and execute audits to identify gap analysis
- To lead on submissions for new Medical Devices
- To coordinate the review and documentation of intended uses for each product
- To inform and educate internal partners of new and revised EU regulatory standards
- Being the main regulatory point of contact for product and process risk management
If you have knowledge of the national and international medical device regulatory requirements this would be beneficial but full training will be given to someone with the right aptitude and willingness to learn
You must be a fast learner, possess strong administration skills. A background in bio-science, regulatory or quality would be ideal but not essential
In return the company are offering a salary from GBP25,000 to GBP35,000 DOE
Hrs are 8am to 430pm Mon to Thurs and 8am to 330pm on Friday's
To find out more about this fantastic and rare opportunity please call Sally Appleby at the Truro, Cornwall Berry Recruitment Branch for more information
Please note that no terminology in this advert is intended to discriminate on the grounds of a person's gender, marital status, race, religion, colour, age, disability or sexual orientation. Every candidate will be assessed only in accordance with their merits, qualifications and ability to perform the duties of the job
If you are from a strong administrative, medical devices, regulatory or quality background we would love to hear from you!
Joining a friendly team and reporting to the Regulatory Affairs Executive you will be responsible for:
- Compiling and maintaining the Technical Documentation Files
- Plan and execute audits to identify gap analysis
- To lead on submissions for new Medical Devices
- To coordinate the review and documentation of intended uses for each product
- To inform and educate internal partners of new and revised EU regulatory standards
- Being the main regulatory point of contact for product and process risk management
If you have knowledge of the national and international medical device regulatory requirements this would be beneficial but full training will be given to someone with the right aptitude and willingness to learn
You must be a fast learner, possess strong administration skills. A background in bio-science, regulatory or quality would be ideal but not essential
In return the company are offering a salary from GBP25,000 to GBP35,000 DOE
Hrs are 8am to 430pm Mon to Thurs and 8am to 330pm on Friday's
To find out more about this fantastic and rare opportunity please call Sally Appleby at the Truro, Cornwall Berry Recruitment Branch for more information
Please note that no terminology in this advert is intended to discriminate on the grounds of a person's gender, marital status, race, religion, colour, age, disability or sexual orientation. Every candidate will be assessed only in accordance with their merits, qualifications and ability to perform the duties of the job