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7 дней назад

Mexico CQ Analyst HSD (MedTech)

Формат работы
hybrid
Тип работы
fulltime
Грейд
junior
Английский
b2
Страна
Mexico
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
Mexico CQ Analyst HSD (MedTech): Supporting quality and regulatory compliance activities for medical device products and systems with an accent on quality documentation, QMS requirements, and regulatory standards. Focus on analyzing quality metrics, tracking deviations and CAPAs, and supporting audits and continuous improvement initiatives.

Location: Mexico City, Mexico; hybrid work arrangement

Company

Johnson & Johnson MedTech develops healthcare and medical device solutions, with DePuy Synthes operating in the orthopaedics sector.

What you will do

  • Support quality and compliance activities in line with internal procedures and regulatory requirements.
  • Prepare, review, and maintain quality procedures, records, trackers, and other documentation.
  • Monitor and follow up on deviations, nonconformances, and corrective and preventive actions.
  • Compile and analyze quality data and metrics for reporting and continuous improvement.
  • Support audits, inspections, and assessments by organizing documentation and responding to information requests.
  • Maintain quality-system records and collaborate with cross-functional partners on QMS compliance.

Requirements

  • Bachelor’s degree in Engineering, Life Sciences, Quality, Regulatory Affairs, or a related field.
  • 0–2 years of relevant experience in quality, compliance, regulated industries, or analytical roles.
  • Basic knowledge of quality systems and compliance principles, with strong attention to detail.
  • Ability to analyze basic data, prepare clear reports, follow procedures, and collaborate in a team.
  • Spanish is required; English proficiency is preferred.
  • Minimal domestic travel may be required, at less than 10%.

Nice to have

  • Experience in medical devices, pharmaceuticals, or another regulated industry.
  • Familiarity with QMS, ISO standards, audits, inspections, or quality improvement initiatives.
  • Experience with spreadsheets and document management systems.
  • Quality-related certifications such as Lean or Six Sigma.

Culture & Benefits

  • Inclusive work environment focused on individual dignity, diversity, and equal opportunity.
  • Exposure to quality systems within a global medical device organization.
  • Opportunity to support products, processes, and systems subject to regulatory requirements.
  • Accommodation support is available during the interview process for applicants with disabilities.

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