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Regulatory Affairs Associate

Alameda, CA 94502

Posted: 01/09/2023 Employment Type: Contract Job Category: Regulatory Sciences and Medical Writing Job Number: 539077 Is job remote?: No Country: United States

Job Description


target PR: 50-57/hr
Regulatory Affairs Associate
This job role will be based in Alameda, reporting into the Europe, Middle East, Africa and Pakistan regulatory team.  The successful individual will be responsible for authoring and maintaining regulatory submissions for Europe and UK for medical devices (Class IIa/IIb) and IVDs (Class A-C) and may also be required to support other countries in the region.  Working with state-of-the-art products and leading technology, the individual will be responsible for management of design changes, including but not limited to conducting regulatory impact assessments, review and approval of labelling, design documentation, clinical evaluation and working with the global team to implement changes in line with the business strategy.  Role will also include assessment and implementation of new regulations. Requires an advanced degree in science, engineering or related discipline and a minimum of 3 years experience working in a regulated environment.  Experience with global regulations and/or CE marking beneficial.  Relies on experience and judgment to plan and accomplish goals. Performs a variety of tasks. May lead and direct the work of others. A wide degree of creativity and latitude is expected.  Typically reports to a manager.

BACKGROUND:
  • RA Associate with 2-3 years regulatory experience (or 1-2 yrs with a QA / R&D background)
  • RA Associate with 3+ years regulatory experience
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