RQM+ is looking for a Regulatory Affairs / Quality Assurance Associate/Specialist Contractor to support regulatory and quality initiatives for medical products. This is a contract role within the United States.
What You'll Do
- Support regulatory submissions and compliance activities
- Assist in maintaining and improving quality management systems
- Conduct document reviews and audits to ensure regulatory standards are met
- Provide quality and regulatory guidance to project teams
What We're Looking For
- Proven experience in regulatory affairs or quality assurance within a medical device or pharmaceutical setting
- Strong knowledge of FDA regulations and ISO quality standards
- Ability to manage multiple projects and work independently
- Excellent written and verbal communication skills
Work Mode
This is a fully remote contractor position open to candidates located anywhere within the United States.
RQM+ is an equal opportunity employer.
