Onsite Document Control Specialist – GMP/Quality

MADE Scientific Inc; Princeton (NJ); Presencial; USD 60.000 - 85.000; Jornada completa

Descripción de la vacante

MADE Scientific Inc. in Princeton, NJ is seeking a Document Control Specialist to manage GMP and quality documentation, ensuring audit readiness. The role requires strong organization, attention to detail, and collaboration across teams to maintain confidential, compliant records in a regulated environment.

The position is full-time and on-site in Princeton, offering opportunities to support internal audits and continuous improvement of document workflows within a CDMO setting.

Formación

• Experience in GMP document control is preferred.
• Ability to manage high volumes of documentation in a regulated environment.
• Biotech/pharma CDMO experience is a plus.

Responsabilidades

• Organize and maintain the document control room and storage areas.
• Issue, reconcile, and archive GMP documents and training records.
• Maintain document traceability and archival records.
• Assist during audits by retrieving requested documentation.
• Support cross-functional teams with document requests.

Conocimientos

Org skills

Attention to detail

Communication

MS Word

MS Excel

Outlook

Document control

GMP knowledge

Educación

Associate or Bachelor's degree

Herramientas

Microsoft Office Suite

Descripción del empleo

MADE Scientific Inc. in Princeton, NJ is seeking a Document Control Specialist to manage GMP and quality documentation, ensuring audit readiness. The role requires strong organization, attention to detail, and collaboration across teams to maintain confidential, compliant records in a regulated environment.

The position is full-time and on-site in Princeton, offering opportunities to support internal audits and continuous improvement of document workflows within a CDMO setting.