CQ Sr. Analyst Techno-vigilance, Mexico

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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 .

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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, Mexico City, Mexico

Job Description:

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.

DePuy Synthes is recruiting for a CQ Sr.

Analyst Techno-vigilance, Mexico located in Mexico City, DF, Mexico

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.


* P...