Job title & location
mexico cq analyst hsd – mexico city, ciudad de méxico, mexico.
job summary
the mexico cq analyst hsd supports quality and regulatory affairs (qara) activities within depuy synthes by assisting with quality compliance processes, documentation, and continuous improvement initiatives. This role plays a key part in ensuring products, processes, and systems meet internal quality standards and applicable regulatory requirements.
key responsibilities
* support the execution of quality and compliance activities in alignment with internal procedures and regulatory requirements.
* assist with the preparation, review, and maintenance of quality documentation, including procedures, records, and trackers.
* participate in the monitoring and follow‑up of 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 with cross‑functional partners to support compliance with quality management system (qms) requirements.
* maintain accurate records and ensure timely updates within quality systems and databases.
qualifications
* education: bachelor’s degree required in engineering, life sciences, quality, regulatory affairs, or a related field. Advanced degree preferred but not required.
* experience: 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 qualifications
* prior exposure to medical device, 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.
* proficiency with standard office and documentation tools (e.g., spreadsheets, document management systems).
* effective written and verbal communication skills.
other requirements
* languages: spanish required; english proficiency preferred.
* travel: minimal travel may be required (less than 10%), primarily domestic.
* certifications: quality‑related certifications (e.g., lean, six sigma, internal quality training) preferred but not required.
equal opportunity employer
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.
#j-18808-ljbffr