[Hiring] Regulatory Affairs Specialist @Three Point Solutions, Inc.

Role Description

Direct or performs coordination and preparation of document packages for regulatory submissions related to the MiniMed separation from all areas of company, internal audits and inspections.

• Lead and compile all materials required in submissions related to the MiniMed separation.
• Monitor and improve tracking as well as control systems.
• Update regulatory approval data in various systems to ensure data is kept up to date.
• Keep abreast of regulatory procedures and changes.
• May direct interaction with regulatory agencies on defined matters.

Qualifications

• Bachelor's degree in Life Sciences, Engineering, Chemistry, or a related technical field.
• 2-5 years of regulatory affairs experience within the medical device industry.

Company Description