Senior Document Control & Change Analyst (MedTech)

Johnson & Johnson; Ciudad Juárez; Presencial; MXN 360.000 - 600.000; Jornada completa

Descripción de la vacante

Johnson & Johnson in Ciudad Juárez is seeking a Senior Document Control Change Analyst (Fixed Term: 12 months) to ensure proper execution of change control for quality system documents in the PLM system, and to support site records management.

You will analyze changes, review requests, proofread, translate Quality System documents, train users, and contribute to audits with FDA, ISO, and internal teams. This role emphasizes accuracy, compliance, and collaboration across functions.

Formación

• High School Diploma and/or technical career.
• Close to completion of college career or recently finished and related work experience.

Responsabilidades

• Analyze documentation changes based on description/rationale and the sites/functions affected.
• Review accuracy and consistency of document changes submitted.
• Review Change Requests/Change Notices in a timely manner.
• Proofread and edit documents for style, grammar, spelling, format, ensuring GDPs.
• Complete Quality System policy and procedure translations as required.
• Collaborate with relevant personnel to ensure accuracy of document revisions.
• Provide training/guidance to change originators, system users, and other internal customers in change control processes and system tools.
• Execute and support activities associated with Records Management program/procedures.
• Generate Document Change Control/Records Management reports as needed.
• Support implementation of Quality Systems initiatives and process improvements as required.
• Support Quality Systems audits; FDA, ISO/ TUV, Internal, etc.

Conocimientos

Document control

Change control

Quality systems

Educación

High School Diploma or technical career

Close to completion of college or related work experience

Herramientas

PLM system

Descripción del empleo

Johnson & Johnson in Ciudad Juárez is seeking a Senior Document Control Change Analyst (Fixed Term: 12 months) to ensure proper execution of change control for quality system documents in the PLM system, and to support site records management.

You will analyze changes, review requests, proofread, translate Quality System documents, train users, and contribute to audits with FDA, ISO, and internal teams. This role emphasizes accuracy, compliance, and collaboration across functions.