QMS Document Control Specialist - ISO 9001

Odysea LLC; New Iberia (LA); Presencial; USD 60.000 - 80.000; Jornada completa

Descripción de la vacante

Odysea LLC is seeking a Document Control Specialist to coordinate and manage document control within the Quality Management System. You will support ISO 9001 compliant manufacturing processes and ensure documentation accuracy across projects.

Responsibilities include maintaining electronic and hard copy systems, guiding teams on QA records, assisting internal audits, and driving continuous improvement in documentation practices.

Formación

• High School Diploma or equivalent; technical degree preferred.
• Experience with ISO 9001 compliant manufacturing.
• Strong skills in Microsoft Office.
• Dependable with organizational and communication abilities.
• ISO 9001 Internal Auditor certification preferred.
• Six Sigma Yellow Belt desired.
• Experience in industrial/manufacturing environments desirable.
• Familiarity with Ideagen QMS (QPulse) or similar.

Responsabilidades

• Establish and manage document control systems for project documents.
• Handle document flow, revision, and archiving in QPulse or equivalent.
• Assist internal audits and ISO 9001 certification processes.
• Collaborate with departments to ensure QA and QC documentation.
• Support quality and regulatory compliance activities.
• Maintain organized records with timely updates and revisions.
• Communicate across teams to resolve documentation issues.
• Provide training on document control practices as needed.
• Demonstrate strong communication, problem-solving, and organizational skills.

Conocimientos

ISO 9001 compliance

Document control

Microsoft Office

Strong communication

Independent work

Educación

High School Diploma or equivalent

Technical college degree preferred

ISO 9001 Internal Auditor certification

Six Sigma Yellow Belt

Herramientas

Ideagen QMS (QPulse)

Descripción del empleo

Odysea LLC is seeking a Document Control Specialist to coordinate and manage document control within the Quality Management System. You will support ISO 9001 compliant manufacturing processes and ensure documentation accuracy across projects.

Responsibilities include maintaining electronic and hard copy systems, guiding teams on QA records, assisting internal audits, and driving continuous improvement in documentation practices.