Hi,
We are currently looking for candidates for an RA Specialist opening in San Diego, CA. Please read carefully the description below and send me your CV or resume if you are interested and very important that meet ALL of the key requirements for this position. Candidates that do not meet the requirements below will not be considered.
FUNCTION STATEMENT
Support the Regulatory Affairs international registration activities for drug products and medical devices.
POSITION SUMMARY
Reports to the Associate Director of Regulatory Affairs Department. Responsible for the gathering of documentation required by the Regulatory Authorities worldwide for the successful registration and maintenance of regulatory applications.
REQUIREMENTS
- Bachelor Degree in Science.
- At least 2 years of experience in a Regulatory, QA and/or QC position within the pharmaceutical or medical device industry.
- Basic knowledge of medical devices and/or drug products regulations and GMP's.
- Experience handling regulatory registrations of medical devices and/or drug products is highly desirable.
- Excellent technical writing skills and computer literate.
- Considerable communication skills at all levels and with diverse individuals and groups.
- Excellent employee relations and organization skills.
- Must have collaboration skills, team player and willingness to take on responsibilities and challenges.
Thanks!
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Wilberto Robles
United States
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