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Robert Half International Regulatory Affairs Coordinator in Goleta, California


We currently have an opening for a highly-skilled Regulatory Affairs Coordinator, who will provide support with various administrative duties in the Regulatory Affairs department at a growing medical device company. Are you a hard worker who loves handling multiple projects at once with a positive outlook? Then this may be the right opportunity for you!

What we are looking for:

• Prepare portions of US, EU or international product registrations for a range of globally regulated products

• Plan, coordinate and assist in product information requests from global partners.

• Participate in project team meetings as a regulatory representative.

• Coordinate and compile regulatory submissions.

• Track of global registration status of all products, managing change assessments and generating summary reports.

• Maintain a well-organized and efficient filing system of regulatory records

• Ensure compliance with regulations and guidelines as well as company SOP's and protocols

• Support internal and external regulatory audits, as required.

• Other activities, as assigned.


Requirements for this role:

• Bachelors' degree preferably in a scientific related discipline. Advanced degree preferred.

• 1-3 years related experience in health-care related industries (pharma, IVD or medical devices), preferred. •

• Medical device industry preferred.

• Prior experience as a project leader with strong project management skills, preferred.

• Some expertise in product development or regulatory processes preferred.

• Excellent communication skills demonstrated through technical writing experience is a must.

Please send your resume to for immediate consideration!

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Salary: $17.00 - $19.00 / Hourly

Location: Goleta, CA

Date Posted: January 8, 2021

Employment Type: Temporary

Job Reference: 01260-0011610529

Staffing Area: Office u0026 Administrative