Regulatory Affairs Specialist – Medical Devices
Contract until December 2022
Inside IR35
Berkshire based – flexible working considered
0-2 years Regulatory Medical Device experience
Offering up to £22.50 Per Hour via PAYE
CPL Life Sciences is collaborating with a leading Pharmaceutical organisation who are seeking a Regulatory Affairs Specialist to join their established team working with their Medical Device portfolio.
Supporting the Regulatory Affairs Manager, you will be supporting and ensuring compliance of their devices with regulatory agency regulations and interpretations. This is an ideal opportunity for someone with 1-2 years Medical Device experience who are keen on expanding their skill set with one of the top leaders in the pharmaceutical industry.
Job Responsibilities include;
• Provides solutions to a variety of problems of moderate scope of complexity.
• Prepares necessary outlines, summaries, status reports, memos, graphs, charts, tables, and slides.
• Conducts searches of existing files for requested information.
• Maintains and archives all EU regulatory documentation.
• Responsible for communicating business related issues or opportunities to next management level
• Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures
• Partners with internal and external local, regional and global business partners, including Notified Bodies, Competent Authorities and Trade Associations.
• May take certain responsibilities in the Ethicon EU Authorized Representative organization and act as Local Actor Administrator
Candidate Requirements include;
- Eligibility to live and work in the united Kingdom
- 0-2 experience with a medical device or medical field industry
- Verbal and written communication skills (English – advanced, German – highly advantageous to have)
If this opportunity is of interest to yourself please forward your up to date CV to [email protected]