PM Eligibility, Rationalization & Compliance
Johnson & Johnson · São Paulo, Brazil +1 more
OtherFull-timeCompany career page
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Role summary
Johnson & Johnson's DePuy Synthes seeks a regulatory professional to manage product eligibility assessments, portfolio rationalization, and compliance across international markets. The role supports global strategies through cross-functional collaboration and lifecycle management in medical devices.
What they're looking for
- Bachelor's degree in Life Sciences, Engineering, Regulatory Affairs, Quality, or related field
- Experience supporting product management, regulatory, quality, or compliance in medical devices
- Working knowledge of international regulatory frameworks and product lifecycle management
- Ability to analyze complex data sets for eligibility and rationalization decisions
- Fluency in English required; Spanish strongly preferred
- Advanced degree or regulatory/quality certification preferred
- Experience with medical device regulations in Latin America or global matrixed environments
What you'll be doing
- Lead product eligibility assessments to determine regulatory readiness and market viability internationally
- Execute portfolio rationalization activities including regulatory, quality, and business risk analysis
- Ensure ongoing regulatory compliance of products throughout lifecycle per international requirements
- Partner with Regulatory Affairs, Quality, Supply Chain, and Commercial teams on product strategies
- Maintain compliance documentation, trackers, and databases for audit and inspection readiness
Privacy & handoff
This role links to Johnson & Johnson's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.