CQ Regional Sr. Supervisor

Johnson Johnson; São Paulo; On-site; BRL 180,000 - 270,000; Full time

Job summary

Johnson & Johnson in Sao Paulo, Brazil, is recruiting a CQ Sr. Supervisor - Mkt Quality Regional. The role supports quality compliance processes, works with LATAM regional teams, and helps ensure products and systems meet regulatory requirements.

You will lead quality governance, drive process simplification, and work with cross‑functional partners in Commercial and Quality, with limited travel and opportunities for growth in Quality and Compliance.

Qualifications

• Graduation in pharmacy, engineering, or scientific discipline.
• Minimum 5 years experience in Quality for Medical Devices/Pharma/Consumer products.
• Basic knowledge of quality systems and compliance principles.
• Strong attention to detail and ability to document and track information.
• Able to analyze data and prepare summaries or reports.
• Able to work collaboratively and follow procedures.

Responsibilities

• Regional partner with Commercial and Quality at local level for LATAM quality elements.
• Lead Quality Analyst to execute doc control, training and metrics for LATAM.
• Lead regional quality systems governance model and define regional deployment strategies.
• Define and implement LATAM quality process models, including Master Data/System Administration.
• Shape the Quality Process environment with focus on simplification and new ways of working.
• Oversee key processes related to Marketing Quality and Operations (DSI, NPI, QSMR, Stop Shipment/Recall).

Skills

Quality experience

Documentation

Analytical skills

Team collaboration

Attention to detail

Audits

Education

Graduation in pharmacy/engineering/science

Tools

Office tools

QMS

ISO standards

Job description

Job Function

Quality

Job Sub Function

Customer/Commercial Quality

Job Category

Professional

All Job Posting Locations

São Paulo, Brazil

Job Description

DePuy Synthes is recruiting for a CQ Sr. Supervisor - Mkt Quality Regional, located in Sao Paulo, SP, Brazil.

Job Overview

The CQ - Mkt Quality Support Hub supports Quality activities within DePuy Synthes by assisting with quality compliance processes, documentation, and continuous improvement initiatives. This role plays a key part in helping ensure products, processes, and systems meet internal quality standards and applicable regulatory requirements. The position offers hands‑on exposure to quality systems in a global medical device organization and provides a strong foundation for growth in Quality and Compliance.

Key Responsibilities

• Regional partner working in collaboration with Commercial areas and Quality at local level related to the following Quality System Elements; Stop Shipment/Filed Action, Internal Audit Program, doc control, training and KPIs for LATAM region.
• Lead Quality Analyst to execute quality elements related to Doc Control, training and Metrics for LATAM.
• Lead regional quality systems governance model, including local quality SMEs representing related quality elements and pointing their participation at global forums. Consolidate information and define regional strategies for deployment.
• Define and implement quality process models for LATAM, such as; Quality aspect in Master Data/System Adm.
• Shape the Quality Process environment, with focus on simplification and creating new ways of working.
• Oversite of key process related to Mkt Quality and Operations such as; Customer Services (DSI), NPI, QSMR, Stop Shipment/Recall

Qualifications

Education

• Required: Graduation in pharmacy, engineering, or scientific discipline.

Experience and Skills

• Minimum of 5 years’ experience in the Quality Area related to Medical Devices, Pharmaceutical or Consumer products
• 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

• 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

• Languages: Spanish and English required.
• Travel: Minimal travel may be required (less than 10%), Regional LATAM scope

Johnson & Johnson announced plans to separate our Orthopaedics business to establish a standalone orthopaedics company, operating as DePuy Synthes. The process of the planned separation is anticipated to be completed within 18 to 24 months, subject to legal requirements, including consultation with works councils and other employee representative bodies, as may be required, regulatory approvals and other customary conditions and approvals. Should you accept this position, it is anticipated that, following conclusion of the transaction, you would be an employee of DePuy Synthes and your employment would be governed by DePuy Synthes employment processes, programs, policies, and benefit plans. In that case, details of any planned changes would be provided to you by DePuy Synthes at an appropriate time and subject to any necessary consultation processes.

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 https://www.jnj.com/contact-us/careers, internal employees contact AskGS to be directed to your accommodation resource.

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Preferred Skills

Audit Management, Business Savvy, Coaching, Communication, Compliance Management, Continuous Improvement, Fact-Based Decision Making, ISO 9001, Issue Escalation, Problem Solving, Quality Control (QC), Quality Management Systems (QMS), Quality Standards, Regulatory Environment, Standard Operating Procedure (SOP)