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PM Eligibility, Rationalization & Compliance

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.

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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:
Regulatory Affairs Group

Job Sub Function:
Regulatory Affairs

Job Category:
People Leader

All Job Posting Locations:
Las Condes, Santiago,, Region Metropolitana de Santiago, Chile, São Paulo, Brazil

Job Description:

DePuy Synthes is recruiting for position, located in Sao Paulo, Brazil.

 

Alternate Hybrid locations may be considered at Las Condes, Chile.

Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements.

While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s):

Sao Paulo, Brazil - Requisition Number: R-097924

Las Condes, Chile - Requisition Number: R-099896

Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.

Job Overview 

The PM Eligibility, Rationalization, Compliance role within QARA International plays a critical role in ensuring that DePuy Synthes products remain eligible, compliant, and optimally positioned across international markets.

This position supports global and regional strategies by managing product eligibility assessments, driving portfolio rationalization activities, and ensuring ongoing regulatory compliance throughout the product lifecycle.

The role offers strong cross‑functional exposure and the opportunity to influence portfolio decisions that directly impact patient access and business continuity. 

  

Key Responsibilities 


* Lead and support product eligibility assessments to determine regulatory readiness and market viability across international markets. 



* Execute portfolio rationalization activities, including analysis of regulatory, quality, and business risks to support informed decision‑making. 



* Ensure ongoing regulatory compliance of products throughout their lifecycle in alignment with international and local requirements. 



* Partner closely with Regulatory Affairs, Quality, Supply Chain, and Commercial teams to align product strategies an...




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