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Healthtech • Biotech • Pharmaceutical • Manufacturing
Leads pharmacovigilance quality assurance audits, assessments, and inspection support in GxP-regulated environments. Manages complex audits, CAPA activities, audit planning, training, coaching, and inspection readiness. Supervises junior auditors and contractors, advises business partners on quality and compliance, interprets regulations, conducts peer reviews, and leads cross-functional projects. The role requires approximately 25% domestic and international travel.
Healthtech • Biotech • Pharmaceutical • Manufacturing
Leads global regulatory labeling strategy and development for pharmaceutical products, including target labeling, CCDS, USPI, EUPI, patient labeling, and derived documents. Partners with regulatory, clinical, safety, commercial, medical affairs, and market access teams; guides health authority discussions; manages labeling working groups, governance presentations, inspections, audits, compliance, risk mitigation, and process improvements.
One Month AgoSaved
Healthtech • Biotech • Pharmaceutical • Manufacturing
The IRDP Internship program at Johnson & Johnson is for MBA and master's students, focusing on leadership in healthcare innovation through real business projects and development opportunities.
