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 offershands‑onexposure 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 andfollow‑upof 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 withcross‑functionalpartners to support compliance with Quality Management System (QMS) requirements.

• Maintainaccuraterecords and ensuretimelyupdates within quality systems and databases.

Qualifications

Education

• Bachelor’s degreerequiredin Engineering, Life Sciences, Quality, Regulatory Affairs, ora relatedfield.

• Advanced degree preferred but notrequired

Experience and Skills

Required:

• 0–2 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 medicaldevice,pharmaceutical, 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: Spanishrequired; Englishproficiencypreferred.

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

• Certifications:Quality‑relatedcertifications (e.g., Lean, Six Sigma, internal quality training) preferred but notrequired

For more information on how we support the whole health of our employees throughout their wellness,careerand life journey, please visit www.careers.jnj.com