Onsite GMP Document Control Associate

HireLifeScience; West Greenwich (RI); On-site; USD 42,000 - 52,000; Full time

Job summary

HireLifeScience seeks an Admin/Document Control Specialist for our fully onsite Rhode Island site. You will maintain all required GMP documentation under Quality Management with coaching from the Document Management Subject Matter Expert.

This role focuses on accurate record-keeping and strict adherence to GMP practices. Responsibilities emphasize document control within the GMP framework, ensuring compliance with the Quality System and supporting admin operations during standard hours at the RI

Qualifications

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

Responsibilities

• Maintain all required documentation for the Rhode Island site under Quality Management with coaching from the DM SME.
• Provide comprehensive services in GMP within Document Management and adapt to needs within the Quality System space.

Skills

GMP experience

Document management

Regulated industry experience

Attention to detail

Education

Associate degree

Job description

HireLifeScience seeks an Admin/Document Control Specialist for our fully onsite Rhode Island site. You will maintain all required GMP documentation under Quality Management with coaching from the Document Management Subject Matter Expert.

This role focuses on accurate record-keeping and strict adherence to GMP practices. Responsibilities emphasize document control within the GMP framework, ensuring compliance with the Quality System and supporting admin operations during standard hours at the RI