Content Compliance Moderator

This job is with Johnson & Johnson, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community.

Please do not contact the recruiter directly.


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

Job Function
Medical Affairs Group

Job Sub Function
Medical Affairs

Job Category
Scientific/Technology

All Job Posting Locations:
Bogotá, Distrito Capital, Colombia, Buenos Aires, Argentina, Mexico City, Mexico, Panama, Panamá, Panama

Job Description
About Innovative Medicine
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.

Visionaries like you work on teams that save lives by developing the medicines of tomorrow.

Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.

Learn more at

We are searching for the best talent for Content Compliance Moderator (fixed term - 12 months) to be in Bogotá, Panamá City, Mexico City or Buenos Aires.
You Will Be Responsible For
Responsible for Promotional Content Review Process activities, including:

• Managing adherence to the Promotional Content Review process timeline
• Management of Promotional Content Review using the Promotional Content Review System Review Management
• Makes final determination on the outcome of reviewed Promotional Content Review materials - Sign-off
• Confirms final approved Promotional Content Review materials reflect the outcome of CAC review and approval:
• Changes required during CAC review are incorporated into Promotional Content
• Review materials
• Guarantee the Promotional Content Review process timeline for approve materials
• Performs Quality Check (QC) of Promotional Content Review materials submitted for review to ensure he following:
• Adherence to established quality standards
• Complete Promotional Content Review system fields
• Appropriate Reviewer assignments in the Promotional Content Review system
• Participate in the Promotional Material Plan of their respective therapeutic area (TA) to align the future demand and to contribute with the TA´s in the plan
• Manager support in:
• Governance activities
• System enhancement, process oversight, licenses optimization
• System clean-up
• Training
• Communication plan
• Documents: Development and maintain of process and system documentation to support the operation internally and with the stakeholders (including external).
  
  
• Compliance:
• Monitors and ensures appropriate use of policies, processes and procedures including: Development/implementation of corrective action plans for resolution of recurrent issues.
  
  Provides general guidance on how to avoid or deal with similar situations in the future

Qualifications / Requirements
Bachelor's in sciences degree or equivalent required, preferably in Life Sciences (e.g., Biology, Chemistry, Biochemistry, Nursing, and Pharmacy)

One year of experience can be in quality, marketing, or medical affairs, among others.

This experience can also be through an internship.

Intermediate level of English is required

Portuguese is desirable

Desirable experience in pharmaceutical industry, learning agility is necessary to quickly understand and support TAs and products.

Demonstrated track-record of results.

Capability to connect with different stakeholders providing a cooperative and high-performance environment.

High learning and change capability.

Experience in Veeva Promo Mats system is a plus

Effective communication and negotiation skills guarantee a productivity and cohesive process.

Availability to work for a 1 year fixed term contract

Work locations: Bogotá, Panamá City, Mexico City or Buenos Aires