Senior Techno-Vigilance Analyst Pharmacovigilance & Safety

Brighter Signals; Bogotá ciudad; On-site; MXN 700,000 - 900,000; Full time

Job summary

DePuy Synthes in Mexico City seeks a CQ Sr. Analyst Techno-vigilance to support pharmacovigilance and drug safety processes across discovery to regulatory approval, applying scientific and clinical expertise to identify and respond to safety signals. You will collaborate across disciplines, perform RCA, risk assessments, and prepare reports.

Spanish required, English preferred; travel limited. Johnson & Johnson is an Equal Opportunity Employer and promotes an inclusive interview process for

Qualifications

• Minimum 3 years of experience in Pharmacovigilance and techno-vigilance activities.
• Experience with quality management systems (QMS).
• Proficient in adverse event reporting, health intelligence, and safety orientation.
• Strong analytical and problem-solving skills including RCA.
• Knowledge of clinical operations, regulatory affairs, and pharmacovigilance metrics.

Responsibilities

• Conducts root cause analyses and investigations for signal detection and safety monitoring.
• Performs safety monitoring for medical devices and drugs per standards.
• Prepares and delivers reports based on product safety data.
• Implements risk-based systems to identify and manage pharmacovigilance requirements.
• Assesses safety data and signals as part of techno-vigilance activities.
• Provides recommendations to improve processes and systems in pharmacovigilance.
• Responds to inquiries from external stakeholders regarding product information.
• Trains less-experienced colleagues on techniques and responsibilities.

Skills

Pharmacovigilance

Techno vigilance

Quality management systems

Root cause analysis

Clinical operations

Regulatory affairs

Data analysis

Education

Chemistry/Medicine/Pharmacy/ Biomedical engineering

Job description

DePuy Synthes in Mexico City seeks a CQ Sr. Analyst Techno-vigilance to support pharmacovigilance and drug safety processes across discovery to regulatory approval, applying scientific and clinical expertise to identify and respond to safety signals. You will collaborate across disciplines, perform RCA, risk assessments, and prepare reports.

Spanish required, English preferred; travel limited. Johnson & Johnson is an Equal Opportunity Employer and promotes an inclusive interview process for