PM Eligibility, Rationalization, Compliance

Johnson & Johnson

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

Posted 9/23/2026full-timeSão Paulo • BrazilMid-LevelSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in regulatory compliance, product lifecycle management, and portfolio rationalization within the medical device and life sciences sectors. Proficient in analyzing complex data sets and driving process improvements to enhance operational efficiency and compliance.

Highest-signal resume keywords

Regulatory ComplianceProduct Lifecycle ManagementPortfolio RationalizationRegulatory Affairs Certification (RAC)Experience in Medical Device Regulations

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Data AnalysisRegulatory FrameworksQuality SystemsProduct ManagementCompliance Documentation

Soft Skills

CollaborationCommunicationProblem-Solving

Tools & Technologies

Regulatory Management SystemsProduct Lifecycle Management Systems

Certifications & Qualifications

Regulatory Affairs Certification (RAC)Quality Certification

Industry Keywords

Medical DeviceHealthcareLife SciencesInternational MarketsQuality Assurance

About the role

Key responsibilities & impact

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
Ensure ongoing regulatory compliance of products throughout their lifecycle in alignment with international and local requirements
Partner with Regulatory Affairs, Quality, Supply Chain, and Commercial teams to align product strategies and timelines
Maintain and update product compliance documentation, trackers, and databases for audit and inspection readiness
Support health authority interactions related to product changes, renewals, discontinuations, and remediation activities
Identify and drive process improvements to enhance efficiency, transparency, and consistency within eligibility and rationalization workflows

Requirements

What you’ll need

Bachelor’s degree in Life Sciences, Engineering, Regulatory Affairs, Quality, or a related discipline
Minimum 5 years of experience supporting product management, regulatory affairs, quality, compliance, or related activities within a medical device, healthcare, or life sciences environment
Working knowledge of international regulatory frameworks and product lifecycle management
Ability to analyze complex data sets to support eligibility and rationalization decisions
Fluency in English required
Limited domestic and international travel may be required, up to approximately 10%
Spanish strongly preferred
Advanced degree or certification in Regulatory Affairs, Quality Systems, or Business Administration preferred
Experience working in QARA International or global matrixed organizations preferred
Familiarity with medical device regulations across Latin America and other international regions preferred
Prior involvement in portfolio optimization, product discontinuation, or remediation initiatives preferred
Experience using regulatory or product lifecycle management systems preferred
Regulatory Affairs Certification (RAC) or Quality certification preferred but not required

Benefits

Comp & perks

Inclusive work environment
Employee wellness, career, and life support resources
Interview accommodations for applicants with disabilities
Equal employment opportunity protections
Potential transition to DePuy Synthes benefit plans following the planned separation, subject to applicable processes and consultations