CQ Analyst Mexico

DePuy Synthes is recruiting for a CQ Analyst located in Mexico City Mexico or Bogota Colombia.

Job Overview

The Commercial Quality Analyst Mexico supports the execution of quality activities for commercial operations within the Mexican market. This role helps ensure that sales distribution and postmarket activitiescomply withapplicable regulatory requirements quality system standards and internal procedures. The position contributes directly to patient safety regulatory compliance and business continuity while partnering with Commercial Regulatory Affairs and Supply Chain teams.

Key Responsibilities

• Support commercial quality activities to ensure compliance with regulatory requirements quality system standards and internal policies.

• Assistwith postmarket surveillance activities including complaint handling adverse event reporting and field action support.

• Collaborate with Commercial Regulatory Affairs and Supply Chain teams to support compliant product distribution and lifecycle activities.

• Support implementation and adherence to global and local quality procedures work instructions and controls.

• Participate in internal audits external audits and healthauthorityinspections as.

• Monitor quality issues trends and metrics within the local market and support corrective and preventive actions.

• Maintainaccuratequality documentation records and reports related to commercial quality activities.

• Contribute to continuous improvement initiatives to strengthen quality compliance and operational effectiveness.

Qualifications

Education:

• Bachelors degree in Quality Engineering Life Sciences Regulatory Affairs ora relateddiscipline (required).

• Advanced degree in a scientific quality or regulatory field (preferred).

Experience and Skills:

Required:

• Typically2-4 years of experience in Quality Regulatory or Compliance roles within a regulated industry.

• Foundational understanding of quality system requirements and regulatory expectations for commercial operations.

• Experience supporting postmarket surveillance activities audits or inspections.

• Ability to interpret quality procedures and regulatory requirements and apply them to daily activities.

• Strong attention to detail documentation and organizational skills.

• Effective communication and crossfunctional collaboration skills.

Preferred:

• Experience in medical devices healthcare or other highly regulated industries.

• Familiarity with Mexican regulatory and quality requirements (e.g. COFEPRIS).

• Experience working in a multinational or matrixed organization.

• Exposure to health authority interactions or regulatory inspections.

• Quality or Regulatory certifications.

Other:

• Language: Spanish; Englishproficiencypreferred.

• Travel: Limited; occasional domestic travel within Mexico.

• Certifications: Quality or Regulatory certifications preferred but not.

Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race color religion sex sexual orientation gender identity age national origin disability protected veteran status or other characteristics protected by federal state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.

Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants needs. If you are an individual with a disability and would like to request an accommodation external applicants please contact us via internal employees contact AskGS to be directed to your accommodation resource.

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