CQ Sr Analyst Techno-vigilance, Colombia

At Johnson & Johnson,we believe health is everything.

Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions 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...