# CQ Sr Analyst Techno-vigilance, Colombia at Johnson & Johnson

Johnson & Johnson is hiring a CQ Sr Analyst Techno-vigilance, Colombia in Bogotá, Colombia. Level rates it Little AI ●○○○; you can [apply on Level](https://jobsbylevel.com/go/a0a41120-7372-47bf-8014-b84c9ad28ebb?utm_medium=ai-agent).

AI Level 1, AI centrality 0 out of 100. Bogotá, Distrito Capital, Colombia.

## Details

- Company: [Johnson & Johnson](https://jobsbylevel.com/companies/johnson-johnson)
- AI level: AI Level 1 (score 0 out of 100)
- Location: Bogotá, Distrito Capital, Colombia
- Posted: September 22, 2026
- Apply: https://jobsbylevel.com/go/a0a41120-7372-47bf-8014-b84c9ad28ebb?utm_medium=ai-agent

## Prepare for this job

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## Description

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 Job Description: DePuy Synthes is recruiting for a CQ Sr Analyst Techno-vigilance, Colombia , located in Bogota, Colombia . Job Overview Experienced professional in a scientific or technological field. Supports the operational, medical, and scientific components of the organization’s drug safety and techno vigilance/pharmacovigilance processes and procedures. Contributes scientific, pharmaceutical, medical devices and clinical expertise, with a strategic focus on identifying, assessing, and responding to safety risks and detecting signals related to the organization’s products. Collaborates across disciplines to actively manage and mitigate risks as clinical, medical and pharmaceutical products progress from discovery and preclinical phases through clinical trials and regulatory approval Key Responsibilities Conducts root cause analyses and investigations related to signal detection and performs safety monitoring activities to identify, assess, and manage risks. Conducts medical devices/drug safety monitoring and follow-up in accordance with the organization’s standards and protocols. Prepares and delivers reports and presentations based on customers’ use of the organization’s products. Implements risk-based systems, with minimal supervision, to identify, assess, and manage techno vigilance /pharmacovigilance requirements. Assesses safety data and signals as part of ongoing techno vigilance/pharmacovigilance activities. Provides recommendations to improve processes and systems supporting the techno vigilance/Pharmacovigilance department’s activities. Responds to inquiries from external stakeholders regarding the organization’s product information and new developments. Trains less-experienced colleagues on techniques, processes, and responsibilities. Qualifications Education Chemistry, medicine, pharmacy (QFB), or biomedical engineering Experience and Skills Required Min 3 years of experience in Pharmacovigilance and Techno vigilance activities Demonstrates skills and competencies in process optimization, quality management systems (QMS) Serious adverse event reporting, report writing, health intelligence, safety orientation Root cause analysis (RCA) Clinical operations, regulatory affairs management, pharmacovigilance, performance measurement, critical thinking, and safety investigations. Other Languages: Spanish required, English proficiency preferred. Travel: Limited domestic or international travel may be required (generally <10%). 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

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