Transportation & Temp Control - LATAM at Johnson &… · São Paulo

TRANSPORTATION & TEMP CONTROL - LATAM Location: São Paulo, Brazil · Hybrid Work At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com. As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit. Job Function: Quality Job Sub Function: Customer/Commercial Quality Job Category: Professional All Job Posting Locations: Bogotá, Distrito Capital, Colombia, Las Condes, Santiago,, Region Metropolitana de Santiago, Chile, Mexico City, Mexico, São Paulo, Brazil Job Description: DePuy Synthes is recruiting for a Transportation & Temp Control - LATAM, located in São Paulo, São Paulo, Brazil or Bogota, Colombia or Mexico City, Mexico or Las Condes, Chile. The Transportation & Temp Control - LATAM supports the execution, maintenance, and continuous improvement of Commercial Quality System Support (CQSS) activities across the Latin America region within QARA International. This role plays a key part in ensuring compliance with global and regional quality system requirements, supporting audit readiness, and partnering with cross‑functional stakeholders to maintain high standards of product quality and patient safety. The position offers strong exposure to regional and global quality systems and the opportunity to make a meaningful impact across the DePuy Synthes portfolio.  Key Responsibilities  • Support day‑to‑day CQSS activities across LATAM, including documentation, tracking, and follow‑up of quality system actions and deliverables.  • Prepare, review, and maintain quality system documentation (e.g., SOPs, work instructions, records) in alignment with global standards and regional requirements.  • Support internal audits, health authority inspections, and quality system reviews, including preparation of evidence and follow‑up of corrective actions.  • Collect, analyze, and trend quality system data and metrics to support continuous improvement and management review activities.  • Assist with investigation, escalation, and remediation of quality system and compliance issues under guidance from senior quality staff.  • Partner with Regulatory Affairs, Commercial, Operations, and other cross‑functional teams to ensure alignment with quality system and compliance requirements.  • Apply DePuy Synthes and Johnson & Johnson quality principles, Credo values, and compliance expectations in all CQSS activities.  Qualifications  Education  • Bachelor’s degree required in Life Sciences, Engineering, Quality, Regulatory Affairs, or a related discipline.  • Advanced degree or quality‑related training preferred.  Experience and Skills  Required  • Generally requires 0–2 years of relevant experience in quality systems, commercial quality, regulatory, or a related regulated environment, aligned to a developing professional‑level role.  • Foundational knowledge of quality systems, documentation practices, and compliance requirements.  • Strong attention to detail with the ability to manage and maintain accurate quality system documentation.  • Ability to analyze basic data and support quality system metrics and trend reporting.  • Ability to work effectively in a cross‑functional, regional, and international environment.  Preferred  • Experience in a regulated industry such as medical devices, pharmaceuticals, or healthcare.  • Familiarity with global quality standards and regulations (e.g., ISO, GxP).  • Exposure to audit or inspection readiness activities.  • Experience using electronic quality management systems or document management tools.  • Experience supporting regional or multi‑country quality initiatives.  • Effective written and verbal communication skills.  Other  • Languages: Portuguese required; English proficiency preferred for regional and global collaboration.  • Travel: Limited regional travel across LATAM may be required (generally <15%).  • Certifications: Quality‑related certifications (e.g., ISO, Six Sigma, CQE) preferred but not required.  For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit www.careers.jnj.com.  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.     #LI-Hybrid  #DePuySynthesCareers      Required Skills:     Preferred Skills: Audit Management, Business Behavior, Coaching, Compliance Management, Continuous Improvement, Data Analysis, Detail-Oriented, Goal Attainment, Internal Controls, Issue Escalation, Problem Solving, Process Oriented, Quality Control (QC), Quality Management Systems (QMS), Quality Standards, Regulatory Environment