Fedramp Documentation And Compliance Specialist Jobs

Excellent organizational, time management, and record keeping skills.

Lead document control requirements for the Regulatory & Quality Teams.

3+ years of experience in registration in cosmetic industry; international registration experience highly desired.

Working knowledge of industry regulations.

Experience in quality control environment a plus.

Advanced excel skills with ability to develop and maintain macro tools.

Manages necessary documentation for CHAP and/or FDA requirements such as annual oxygen prescription renewals.

Collaborates with management team to identify and prioritize quality improvement strategies that affect company operations.

Completes all annual education and competency requirements within the calendar year.

Leverage the skills and abilities of each person to enable great teams.

High school or vocational school graduate or an equivalent combination of education and experience.

Development – We believe equipping you with support and development opportunities is an essential part of delivering a remarkable employment experience. 

- Follow the FedRAMP documentation requirements and templates to ensure consistency and compliance with program guidelines.

- Document the results of the system's risk assessment, including identified risks, associated vulnerabilities, and recommended mitigations.

- Clearly articulate the system's risk posture and how the organization addresses and manages identified risks.

- Maintain accurate and up-to-date records of system monitoring activities, including security incidents, vulnerabilities, and remediation efforts.

- Strong understanding of FedRAMP requirements and documentation guidelines.

- Proven experience in developing system documentation and ensuring compliance with security standards and regulations.