Production Supervisor A - Medical Industry | Terán Terán

North American Production Sharing de México, S.A. de C.V.; Tijuana; Presencial; MXN 360.000 - 540.000; Jornada completa

Descripción de la vacante

North American Production Sharing de México, S.A. de C.V. seeks a Production Supervisor to lead daily manufacturing operations in a regulated environment in Tijuana.

You will ensure schedules are met, safety and quality are prioritized, and resources are aligned with production goals. The role requires 3–5 years in production supervision within Medical Device/biotech/pharma, strong ISO knowledge, and experience with SAP/Oracle, KPIs, CAPA, and Lean.

Formación

• 3–5 years of experience as a Production Supervisor in Medical Device, biotech, or pharma.
• Working knowledge of ISO 9001 and ISO 13485 QMS.
• Experience managing production personnel, equipment, and resources.
• Proficiency with SAP/Oracle or similar MRP/ERP systems.
• Experience monitoring KPIs and production metrics.
• Knowledge of RCA, non-conformance investigations, and CAPA.
• Advanced English required for meetings, reports, and cross-functional work.
• Experience in cleanroom environments and Lean/Six Sigma initiatives.

Responsabilidades

• Lead daily manufacturing operations to meet schedules safely and on time.
• Coordinate personnel, materials, and resources to meet quality and productivity goals.
• Ensure compliance with internal procedures, quality standards, and regulatory requirements.
• Lead investigations on deviations and CAPA implementations.
• Monitor and report production performance using KPIs and metrics.
• Manage employee performance, training, and competency certifications.
• Support workforce planning and development activities.
• Promote safety, quality, accountability, and continuous improvement.
• Drive Lean, 5S, and Six Sigma initiatives to improve efficiency.

Conocimientos

Production supervision

Leadership

Lean manufacturing

Six Sigma

Problem solving

Herramientas

SAP

Oracle

MRP/ERP

Descripción del empleo

We are seeking a Production Supervisor with experience in regulated manufacturing environments to lead daily production operations, ensure compliance with production schedules, and drive quality, safety, and operational performance.

Requirements

• 3 to 5 years of experience as a Production Supervisor or Manufacturing Supervisor in the Medical Device, Biotechnology, or Pharmaceutical industry.
• Working knowledge of ISO 9001 and ISO 13485 Quality Management Systems.
• Experience managing production personnel, equipment, and manufacturing resources.
• Proficiency with MRP/ERP systems such as SAP, Oracle, or similar.
• Experience monitoring and reporting KPIs and production metrics.
• Knowledge of Root Cause Analysis, Non-Conformance Investigations, and CAPA processes.
• Experience training, coaching, and developing production personnel.
• Strong leadership, communication, organization, and problem-solving skills.
• Advanced English level required, with the ability to communicate effectively in meetings, presentations, reports, and cross-functional interactions.
• Ability to work in production and cleanroom environments as required.
• Continuous improvement experience involving Lean Manufacturing, 5S, and Six Sigma methodologies is preferred.

Key Responsibilities

• Lead daily manufacturing operations and ensure production schedules are achieved safely, efficiently, and on time.
• Coordinate personnel, materials, and resources to meet quality, delivery, and productivity objectives.
• Ensure compliance with internal procedures, quality standards, and applicable regulatory requirements.
• Lead investigations related to deviations, non-conformances, root cause analysis, and CAPA implementation.
• Monitor and report production performance through established KPIs and operational metrics.
• Manage employee performance, training plans, and competency certifications.
• Support workforce planning, employee development, and performance management activities.
• Promote a culture of safety, quality, accountability, and continuous improvement.
• Drive Lean Manufacturing, 5S, and Six Sigma initiatives to improve efficiency, reduce waste, and optimize production processes.
• Collaborate with cross-functional teams to ensure customer requirements and production goals are consistently achieved.

Key Competencies

• Leadership and team management
• Results-oriented mindset
• Effective communication
• Analytical problem-solving
• Planning and organization
• Continuous improvement focus
• Quality and compliance orientation