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Regulatory Affairs Specialist

Kansas City, MO

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Regulatory Affairs Specialist
Robert Half

Kansas City
Job #682330929
Robert Half Legal is currently assisting a national client in seeking a Regulatory Affairs Specialist to join their Kansas City location on a 6-8 week project, Responsibilities might include: - Audit/assess multi-year Design History File (including product and software) - Determine any possible risks - Prepare audit/assessment for review - Develop possible remediation strategy This position is expected to begin as soon as the right candidate is found and onboarded. It will require 40 hours a week onsite at the clients location in Kansas City. For immediate consideration, please send an updated resume to ~~~.
Located in major North American and global markets, Robert Half Legal is the premier provider of legal staffing and consulting solutions on a full-time, project, and temporary basis, serving both law firms and corporate legal departments. We also provide project and eDiscovery teams and workspace for a wide range of initiatives, including litigation support, mergers and acquisitions and document review matters. Our dedicated teams' industry experience allows us to quickly match skilled legal professionals with the best available jobs. We offer challenging opportunities, competitive compensation and benefits, and skills-enhancement training.
Call your local Robert Half Legal office at ~~~ to discover more about this position. Apply for this job now or contact our branch office for additional information.
All applicants applying for U.S. job openings must be authorized to work in the United States. All applicants applying for Canadian job openings must be authorized to work in Canada.
© 2018 Robert Half Legal. An Equal Opportunity Employer M/F/Disability/Veterans
By clicking 'Apply Now' you are agreeing to Robert Half Terms of Use.
Req ID:
Functional Role:
Account Executive/Staffing Manager
Kansas City
Postal Code:
$28.00 to $28.00 per hour
- 5 years of experience in regulatory affairs - 3 years of experience in IVD or medical device manufacturing environment - Strong knowledge of 21 CFR Part 820.30 Design Controls - Strong knowledge/experience conducting quality audits - Proficient with Microsoft Office, Word, Excel, PowerPoint
Updated 06/12/2018

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