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6 часов назад

Manager, CQ Lead Mexico & Northern Cluster (MedTech)

Формат работы
hybrid
Тип работы
fulltime
Грейд
lead
Английский
b2
Страна
Mexico/Colombia
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Manager, CQ Lead Mexico & Northern Cluster (MedTech): Supporting quality management systems and compliance activities for orthopedic medical device operations with an accent on audits, documentation control, CAPA, and regulatory readiness. Focus on analyzing quality metrics, implementing corrective actions, and coordinating quality standards across manufacturing, supply chain, regulatory, and quality teams.

Location: Hybrid role based in Mexico City, Mexico, or Bogota, Colombia; up to 10% domestic and international travel. Valid work authorization for the United Kingdom is required.

Company

Johnson & Johnson MedTech develops healthcare and orthopedic solutions, with the role expected to transition to DePuy Synthes following the planned separation of the Orthopaedics business.

What you will do

  • Support the execution, maintenance, and documentation of quality management system processes.
  • Coordinate quality and compliance activities across manufacturing, supply chain, regulatory, and quality functions.
  • Support internal and external audits, inspections, compliance assessments, and regulatory readiness.
  • Maintain quality records, procedures, training materials, and document-control processes.
  • Support investigations, corrective and preventive actions, and continuous improvement initiatives.
  • Analyze quality metrics and trends, prepare stakeholder reports, and promote patient-focused quality.

Requirements

  • Bachelor’s degree in Life Sciences, Engineering, Quality, Regulatory Affairs, Biomedical Sciences, or a related discipline.
  • 2–4 years of experience in regulated quality, compliance, regulatory affairs, or medical devices.
  • Knowledge of quality systems, documentation control, compliance processes, and quality records.
  • Strong analytical, organizational, and problem-solving skills, with experience using Microsoft Office and quality-related systems.
  • English proficiency and valid work authorization for the United Kingdom are required.
  • A valid driver’s license may be required depending on business needs.

Nice to have

  • Experience in medical devices, orthopedics, healthcare, or life sciences.
  • Knowledge of ISO quality standards, quality management systems, and regulatory frameworks.
  • Experience with audits, inspections, CAPA, change management, training compliance, and quality data analysis.
  • ASQ, RAC, Lean Six Sigma, or similar quality certification.
  • Experience in a global, matrixed organization.

Culture & Benefits

  • Inclusive work environment guided by the company’s Credo.
  • Cross-functional collaboration supporting safe and innovative orthopedic solutions.
  • Opportunity to contribute to continuous improvement, operational excellence, and patient safety.
  • Domestic and international travel of up to 10% based on business needs.

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