Mexico CQ Analyst HSD

The Mexico CQ Analyst HSD supports Quality and Regulatory Affairs (QARA) activities within DePuy Synthes byassistingwith quality compliance processes documentation and continuous improvement initiatives. This role plays a keypartin helping ensure products processes and systems meet internal quality standards and applicable regulatory requirements. The position offershandsonexposure to quality systems in a global medical device organization and providesa strong foundationfor growth in Quality and Compliance.

Key Responsibilities

• Support the execution of quality and compliance activities in alignment with internal procedures and regulatory requirements.

• Assistwith the preparation review and maintenance of quality documentation including procedures records and trackers.

• Participate in the monitoring andfollowupof quality events such as deviations nonconformances and corrective and preventive actions (CAPA).

• Compile and analyze basic quality data and metrics to support reporting and continuous improvement efforts.

• Support internal audits inspections and assessments by organizing documentation and responding to information requests.

• Collaborate withcrossfunctionalpartners to support compliance with Quality Management System (QMS) requirements.

• Maintainaccuraterecords and ensuretimelyupdates within quality systems and databases.

Qualifications

Education

• Bachelors degreein Engineering Life Sciences Quality Regulatory Affairs ora relatedfield.

• Advanced degree preferred but not.

Experience and Skills

Required:

• 02 years of relevant work experience in quality compliance regulated industries or related analytical roles.

• Basic knowledge of quality systems and compliance principles.

• Strong attention to detail and ability to accurately document and track information.

• Ability to analyze basic data and prepare clear summaries or reports.

• Ability to work collaboratively in a team environment and follow established procedures.

Preferred:

• Priorexposure to medicaldevicepharmaceutical or other regulated industries.

• Familiarity with Quality Management Systems (QMS) and regulatory standards (e.g. ISO internal quality procedures).

• Experience supporting audits inspections or quality improvement initiatives.

• Proficiencywith standard office and documentation tools (e.g. spreadsheets document management systems).

• Effective written and verbal communication skills.

Other:

• Languages: Spanish; Englishproficiencypreferred.

• Travel: Minimal travel may be(less than 10%) primarily domestic.

• Certifications:Qualityrelatedcertifications (e.g. Lean Six Sigma internal quality training) preferred but not.

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