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PM Eligibility, Rationalization & Compliance
Johnson & Johnson. Lead and support product eligibility assessments to determine regulatory readiness and market viability across international markets .
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in regulatory compliance, product lifecycle management, and portfolio optimization within the medical device and life sciences sectors. Proficient in cross-functional collaboration and effective communication to drive product strategies and ensure market readiness.
Highest-signal resume keywords
Regulatory ComplianceProduct Lifecycle ManagementPortfolio OptimizationRegulatory Affairs Certification (RAC)Data Analysis
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Regulatory FrameworksQuality SystemsProduct ManagementCompliance DocumentationData AnalysisProcess ImprovementMedical Device RegulationsPortfolio RationalizationEligibility AssessmentsAudit Readiness
Soft Skills
Effective CommunicationOrganizational SkillsCross-Functional CollaborationStakeholder ManagementPrioritization
Tools & Technologies
Regulatory Management SystemsProduct Lifecycle Management Systems
Certifications & Qualifications
Regulatory Affairs Certification (RAC)Quality Certification
Industry Keywords
Life SciencesHealthcareMedical DeviceInternational MarketsQuality AssuranceRegulatory AffairsCompliancePortfolio ManagementMarket ViabilityHealth Authority Interactions
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 throughout the product 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 within eligibility and rationalization workflows
- Influence portfolio decisions affecting patient access and business continuity
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%
- 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
- Spanish strongly preferred
- Effective written and verbal communication skills for cross-functional collaboration
- Strong organizational skills with the ability to manage multiple priorities and stakeholders
Benefits
Comp & perks- Inclusive work environment
- Employee wellness, career, and life support resources
- Accommodation support for applicants with disabilities
- Potential future DePuy Synthes benefit plans and programs following the planned separation, subject to applicable processes and consultations