Regulatory Affairs (RAQA) Documentation Specialist
- Employer
- iMPact Business Group
- Location
- Minneapolis
- Salary
- Competitive
View more
- Industry
- Government and Public Services
- Role
- Other
- Job Type
- Long-Term
- Hours
- Full Time
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Our client, a Global Leader in the Medical Device Industry has an immediate opening for a Regulatory Affairs (RAQA) Documentation Specialist for a 12 month + Contract. Our client offers results-driven people a place where they can make a difference - every day! You will also have the opportunity to work with other like-minded, self-directed and detail oriented Top Talents in an extremely collaborative and professional environment.
Position Description (Principle Duties and Responsibilities)
Co-ordinates and prepares document packages for regulatory submissions from all areas of the organization.
Collects all materials required in submissions, license renewal, and annual registrations.
Keeps abreast of regulatory procedures and changes.
May interact with regulatory agencies.
Works on problems of complex scope where data analysis requires evaluation of specific factors.
Position focused on supporting the EU MDR program.
What you need
BS degree (engineering/technical) with 3years experience in a Regulatory Documentation role.
Medical device industry experience, preferred.
Position Description (Principle Duties and Responsibilities)
Co-ordinates and prepares document packages for regulatory submissions from all areas of the organization.
Collects all materials required in submissions, license renewal, and annual registrations.
Keeps abreast of regulatory procedures and changes.
May interact with regulatory agencies.
Works on problems of complex scope where data analysis requires evaluation of specific factors.
Position focused on supporting the EU MDR program.
What you need
BS degree (engineering/technical) with 3years experience in a Regulatory Documentation role.
Medical device industry experience, preferred.
You need to sign in or create an account to save a job.
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