Associate Quality Assurance

Planet Pharma; West Greenwich (RI); On-site; USD 26,000 - 39,000; Full time

Job summary

Planet Pharma is seeking a documentation-focused professional to maintain site records under Quality Management with coaching from the Document Management SME. The role emphasizes GMP-compliant document handling and flexible support within the Quality System space.

The candidate should have at least an associate degree, basic GMP experience, and proven attention to detail in a regulated environment.

Qualifications

• Associate degree or higher in a related field.
• Basic GMP experience.
• Document management experience.
• Familiar with working in a regulated industry.
• Strong attention to detail.

Responsibilities

• Maintain all required documentation for the site under Quality Management oversight with coaching from the DM SME.
• Provide GMP-compliant document management services and support within the Quality System space as needed.

Skills

Attention to detail

GMP experience

Document management

Education

Associate degree

Tools

Document management system

Job description

Target PR Range: 19-28/hr DOE

Experience: Associates degree at a minimum. Basic GMP experience, Document management experience, Familiar with working within a regulated industry, Strong attention to detail.

Job Details: Responsible for the maintenance of all required documentation for the site under the direction of Quality Management with coaching from the Document Management Subject Matter Expert. Provide comprehensive services in accordance with Good Manufacturing Practices (GMP) within Document Management with ability to flex support as needed within the Quality System space.